Use of chiral auxiliaries in the asymmetric synthesis of biologically active compounds: A review
This review article describes the use of some of the most popular chiral auxiliaries in the asymmetric synthesis of biologically active compounds. Chiral auxiliaries derived from naturally occurring compounds, such as amino acids, carbohydrates, and terpenes, are considered essential tools for the c...
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Published in | Chirality (New York, N.Y.) Vol. 31; no. 10; pp. 776 - 812 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.10.2019
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Abstract | This review article describes the use of some of the most popular chiral auxiliaries in the asymmetric synthesis of biologically active compounds. Chiral auxiliaries derived from naturally occurring compounds, such as amino acids, carbohydrates, and terpenes, are considered essential tools for the construction of highly complex molecules. We highlight the auxiliaries of Evans, Corey, Yamada, Enders, Oppolzer, and Kunz, which led to remarkable progress in asymmetric synthesis in the last decades and continue to bring advances until the present day. |
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AbstractList | This review article describes the use of some of the most popular chiral auxiliaries in the asymmetric synthesis of biologically active compounds. Chiral auxiliaries derived from naturally occurring compounds, such as amino acids, carbohydrates, and terpenes, are considered essential tools for the construction of highly complex molecules. We highlight the auxiliaries of Evans, Corey, Yamada, Enders, Oppolzer, and Kunz, which led to remarkable progress in asymmetric synthesis in the last decades and continue to bring advances until the present day. |
Author | Sartori, Suélen Karine Diaz‐Muñoz, Gaspar Alves Nogueira Diaz, Marisa Rezende, Daniele Cristina Miranda, Izabel Luzia |
Author_xml | – sequence: 1 givenname: Gaspar orcidid: 0000-0002-7515-0420 surname: Diaz‐Muñoz fullname: Diaz‐Muñoz, Gaspar email: gaspardm@qui.ufmg.br organization: Universidade Federal de Minas Gerais – sequence: 2 givenname: Izabel Luzia surname: Miranda fullname: Miranda, Izabel Luzia organization: Universidade Federal de Minas Gerais – sequence: 3 givenname: Suélen Karine surname: Sartori fullname: Sartori, Suélen Karine organization: Universidade Federal de Minas Gerais – sequence: 4 givenname: Daniele Cristina surname: Rezende fullname: Rezende, Daniele Cristina organization: Universidade Federal de Minas Gerais – sequence: 5 givenname: Marisa orcidid: 0000-0002-3370-4149 surname: Alves Nogueira Diaz fullname: Alves Nogueira Diaz, Marisa organization: Universidade Federal de Viçosa |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31418934$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1351/pac199062071241 10.1007/s12039-015-0963-2 10.1016/S0040-4020(97)00412-2 10.1016/0040-4039(88)85179-7 10.1021/ol302761n 10.3390/md8072162 10.1021/ol061671q 10.1016/S0040-4039(97)01336-1 10.1002/chem.200701010 10.1021/ja010302g 10.1021/jacs.8b10364 10.1021/jo00014a052 10.1002/ardp.19122500151 10.1016/j.tet.2012.11.067 10.1016/S0040-4039(99)02131-0 10.1590/S0100-40421997000600015 10.1002/1521-3773(20020517)41:10<1650::AID-ANIE1650>3.0.CO;2-B 10.1002/anie.198910671 10.1039/c39870001053 10.1016/0957-4166(94)80155-X 10.1002/jcb.24785 10.1002/anie.201805370 10.1039/b009029h 10.2174/1385272043369485 10.1002/anie.199303361 10.1016/S0040-4020(02)00080-7 10.1139/v97-010 10.1016/00404-0399(50)1096Z- 10.1021/ja00832a031 10.1055/s-0037-1610148 10.1055/s-0030-1258458 10.1016/0040-4039(95)01312-6 10.1039/C7OB01341H 10.1016/0040-4039(95)00351-C 10.1016/S0040-4020(02)00516-1 10.1002/anie.200805606 10.1055/s-1990-20985 10.1021/ja00099a091 10.1002/9780470134979.ch16 10.1002/anie.197605492 10.1016/S0040-4039(98)01130-7 10.1002/9783527654543.ch1 10.1002/1521-3765(20020916)8:18<4272::AID-CHEM4272>3.0.CO;2-K 10.7164/antibiotics.53.123 10.2165/00002512-200320080-00005 10.1016/j.tetlet.2008.04.130 10.1021/jo00288a029 10.3233/JAD-2010-091621 10.1002/(SICI)1521-3773(19980504)37:8<1044::AID-ANIE1044>3.0.CO;2-E 10.1002/chem.19950010712 10.1021/op900299c 10.1002/9783527619566 10.1021/om700676w 10.1021/ja067264r 10.1021/jo2023119 10.1016/S0960-894X(01)80855-6 10.1016/S0040-4020(99)00964-3 10.1021/ol9003405 10.1002/adsc.201200761 10.1021/jacs.7b13776 10.1093/biolre/iox183 10.1055/s-0034-1380215 10.1021/jo9614811 10.3390/molecules19067429 10.1039/b207130b 10.1039/b701534h 10.1016/j.tetlet.2010.10.141 10.1021/acs.orglett.7b02274 10.1021/ja037643 10.1016/S0040-4039(01)88662-7 10.1039/C39940001151 10.1021/ol006457v 10.1590/S0100-40421998000300012 10.1021/ja00401a031 10.1016/j.jep.2011.07.035 10.1021/jo1019877 10.1016/0378-8741(95)01342-3 10.1002/9783527621071.ch10 10.1016/S0040-4039(01)96647-X 10.1016/S0040-4020(97)00766-7 10.2174/1570179413666160624112433 10.1080/00397911.2018.1458241 10.1016/j.tetlet.2006.05.043 10.1016/j.tetasy.2011.04.014 10.1021/ja01048a062 10.1021/cr990374e 10.1002/anie.198609473 10.1016/S0040-4039(00)82216-9 10.1016/j.tet.2017.09.041 10.1021/jo980942a 10.1055/s-1997-3185 10.1016/S0040-4039(01)95667-9 10.1016/j.tet.2007.10.056 10.1055/s-1991-26641 10.1021/jo0155052 10.1016/j.tet.2013.11.046 10.1095/biolreprod.112.100438 10.1016/S0040-4039(00)61925-1 10.3390/molecules171113330 10.1021/ja002556s 10.1002/jlac.1995199507161 10.1021/ja00210a084 10.1021/ol100969f 10.1021/jacs.5b08207 10.1021/acs.joc.6b00068 10.1038/nature11411 10.1021/jacs.5b10980 10.1021/ja0260014 10.1039/c3ra41718b 10.1002/anie.198705571 10.1021/ol991214s 10.1039/a815113y 10.1021/ja991190k 10.1039/c4ob00443d 10.3390/molecules17021177 10.1039/c2ob25400j 10.1016/j.tet.2011.03.064 10.1021/ja101913k 10.1002/anie.199202881 10.1002/hlca.19770600417 10.1351/pac199567101627 10.1246/bcsj.43.2223 10.1039/j29700001267 10.1016/S0040-4020(00)00337-9 10.1016/0040-4039(91)80116-N 10.1021/acs.joc.6b02838 10.1134/S1068162013060095 10.1021/ja036414k 10.1016/S0040-4020(01)86054-3 10.1016/0040-4039(94)85031-3 10.1021/ja00258a050 10.1002/9783527654543 10.1039/C6RA00653A 10.1021/np034077n 10.1021/acs.orglett.8b01087 10.1039/B617094C 10.1021/jo0001885 10.1016/S0040-4039(00)80504-3 10.1021/ja00856a074 10.1002/ejoc.201101673 10.1021/ja00175a038 10.1021/ja954211t 10.1021/ja00738a045 10.1016/S0040-4039(02)02452-8 10.1021/ja00165a094 10.1002/ardp.19572901002 10.1016/S0040-4039(00)71307-4 10.1021/jo701849x 10.1016/S0140-6736(14)62111-5 10.1021/ja00064a011 10.1016/S0040-4039(01)88663-9 10.1016/j.tet.2009.08.042 10.1016/S0040-4039(97)00482-6 10.1016/j.tet.2012.03.115 10.1016/j.tetlet.2008.10.074 10.1055/s-0032-1316865 10.1016/S0040-4020(01)86544-3 10.1080/09546630410017275 10.1016/j.tetlet.2012.04.042 |
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References | 2010; 12 1990; 55 2013; 3 2013; 69 2010; 14 2017; 82 2002; 19 1995; 36 1987; 109 2015; 385 2011; 52 1975; 97 2012; 17 1970 2012; 14 2012; 489 1989; 49 1957; 290/62 2012; 10 1985; 26 2018; 48 2017; 73 2009; 11 1998; 15 1990; 1990 2010; 20 1997; 51 1971; 93 1994; 304 2015; 137 1997; 53 1971; 12 1993; 32 2006; 26 2008; 25 2013; 355 1983 2014; 19 2011; 67 2000; 122 2007; 63 2014; 12 2010; 8 2011; 137 2018; 29 1991; 1991 2009; 65 1969; 91 2015; 127 1997; 20 2000; 65 1969; 10 2002; 8 2002; 1 1994 1993 1998; 63 1992; 31 1995; 1 2018; 20 2011; 8 2007; 13 2016; 6 1988; 29 2002; 124 2008; 49 2006; 47 1986; 25 1997; 38 2000; 100 1973; 5 1990; 112 1993; 115 2003; 20 1996; 118 2002; 58 2014; 70 2012; 2012 1991; 56 1974; 96 2017; 49 1981; 103 2000; 41 2004; 67 1999; 121 2008; 8 2000; 2 2011; 17 2008; 73 2012; 53 2009; 48 1977; 60 2015; 47 1991; 47 2014; 2 2002; 41 2000; 56 1995; 67 2002; 43 2000; 53 1988; 44 2011; 22 1994; 35 2016; 81 2003; 125 2012; 68 1997; 1997 2007; 26 2005; 36 1987; 14 2010; 75 2001; 123 1994; 116 1997; 62 2007; 129 2018; 140 1991; 32 2013; 45 1996; 50 2009 2006; 8 1912; 250 2007 2005 2004 2001; 66 2019; 141 1998; 21 2012; 77 2010; 1991 2014; 115 1989; 28 1990; 62 1998; 37 1998; 39 2013; 39 2017; 15 2017; 14 1997; 75 2017; 98 2004; 15 1995; 1995 2010; 132 2018 1970; 43 2017; 19 1988; 110 2016; 138 2013 1976; 17 1976; 15 2012; 87 1994; 5 1994; 4 1987; 26 2018; 57 e_1_2_5_27_1 e_1_2_5_166_1 e_1_2_5_120_1 e_1_2_5_147_1 e_1_2_5_23_1 e_1_2_5_46_1 e_1_2_5_162_1 e_1_2_5_124_1 e_1_2_5_101_1 e_1_2_5_143_1 e_1_2_5_65_1 e_1_2_5_88_1 e_1_2_5_128_1 e_1_2_5_105_1 e_1_2_5_69_1 e_1_2_5_109_1 e_1_2_5_80_1 e_1_2_5_61_1 Kunz H (e_1_2_5_169_1) 2010; 1991 e_1_2_5_42_1 Evans DA (e_1_2_5_2_1) 2007 e_1_2_5_15_1 e_1_2_5_38_1 e_1_2_5_132_1 e_1_2_5_178_1 e_1_2_5_11_1 e_1_2_5_34_1 e_1_2_5_57_1 e_1_2_5_113_1 e_1_2_5_136_1 e_1_2_5_151_1 e_1_2_5_7_1 e_1_2_5_76_1 e_1_2_5_99_1 e_1_2_5_117_1 e_1_2_5_19_1 e_1_2_5_159_1 e_1_2_5_91_1 e_1_2_5_72_1 Kurti L (e_1_2_5_82_1) 2005 e_1_2_5_95_1 Srivastava A (e_1_2_5_5_1) 2018 e_1_2_5_30_1 e_1_2_5_49_1 e_1_2_5_146_1 e_1_2_5_26_1 e_1_2_5_45_1 e_1_2_5_100_1 e_1_2_5_123_1 e_1_2_5_142_1 e_1_2_5_22_1 e_1_2_5_165_1 e_1_2_5_87_1 e_1_2_5_104_1 e_1_2_5_127_1 e_1_2_5_68_1 e_1_2_5_108_1 e_1_2_5_60_1 e_1_2_5_83_1 e_1_2_5_64_1 Fakhreddin J (e_1_2_5_3_1) 1993 e_1_2_5_41_1 e_1_2_5_14_1 e_1_2_5_131_1 e_1_2_5_177_1 Hanessian S (e_1_2_5_156_1) 1989; 49 e_1_2_5_158_1 e_1_2_5_8_1 e_1_2_5_10_1 e_1_2_5_56_1 e_1_2_5_135_1 e_1_2_5_33_1 e_1_2_5_112_1 e_1_2_5_4_1 e_1_2_5_98_1 e_1_2_5_139_1 e_1_2_5_79_1 e_1_2_5_116_1 e_1_2_5_18_1 e_1_2_5_90_1 e_1_2_5_71_1 e_1_2_5_94_1 e_1_2_5_75_1 Vilaivan T (e_1_2_5_174_1) 2005; 36 e_1_2_5_52_1 e_1_2_5_180_1 Saeidian H (e_1_2_5_53_1) 2014; 2 e_1_2_5_161_1 Hale KJ (e_1_2_5_150_1) 1993 Zhang Z (e_1_2_5_107_1) 2017; 82 e_1_2_5_145_1 e_1_2_5_25_1 e_1_2_5_48_1 e_1_2_5_168_1 e_1_2_5_103_1 e_1_2_5_141_1 e_1_2_5_21_1 e_1_2_5_44_1 e_1_2_5_164_1 e_1_2_5_122_1 Amjad M (e_1_2_5_32_1) 2006; 26 e_1_2_5_126_1 e_1_2_5_149_1 e_1_2_5_29_1 Hanessian S (e_1_2_5_155_1) 1983 e_1_2_5_63_1 e_1_2_5_86_1 Lehnert T (e_1_2_5_154_1) 2011; 17 e_1_2_5_40_1 e_1_2_5_171_1 e_1_2_5_17_1 e_1_2_5_36_1 e_1_2_5_59_1 e_1_2_5_130_1 e_1_2_5_157_1 e_1_2_5_9_1 e_1_2_5_13_1 e_1_2_5_55_1 e_1_2_5_111_1 e_1_2_5_134_1 e_1_2_5_153_1 e_1_2_5_176_1 e_1_2_5_78_1 e_1_2_5_115_1 e_1_2_5_138_1 e_1_2_5_119_1 e_1_2_5_70_1 e_1_2_5_93_1 e_1_2_5_74_1 e_1_2_5_97_1 e_1_2_5_51_1 e_1_2_5_160_1 Ióca LP (e_1_2_5_37_1) 2018; 29 e_1_2_5_121_1 e_1_2_5_144_1 e_1_2_5_167_1 e_1_2_5_28_1 e_1_2_5_47_1 e_1_2_5_140_1 e_1_2_5_102_1 e_1_2_5_125_1 e_1_2_5_24_1 e_1_2_5_163_1 e_1_2_5_43_1 e_1_2_5_106_1 e_1_2_5_129_1 e_1_2_5_66_1 e_1_2_5_89_1 Cowden CJ (e_1_2_5_84_1) 1997; 51 e_1_2_5_148_1 e_1_2_5_62_1 Tramontini M (e_1_2_5_172_1) 1994 e_1_2_5_85_1 e_1_2_5_170_1 e_1_2_5_20_1 e_1_2_5_39_1 e_1_2_5_110_1 e_1_2_5_16_1 e_1_2_5_58_1 Schaubach S (e_1_2_5_67_1) 2017; 49 e_1_2_5_179_1 Jones S (e_1_2_5_81_1) 2002; 1 e_1_2_5_35_1 e_1_2_5_114_1 e_1_2_5_152_1 e_1_2_5_6_1 e_1_2_5_12_1 e_1_2_5_54_1 e_1_2_5_133_1 e_1_2_5_175_1 e_1_2_5_77_1 e_1_2_5_118_1 Domingo LR (e_1_2_5_96_1) 2009 e_1_2_5_137_1 e_1_2_5_92_1 e_1_2_5_73_1 e_1_2_5_31_1 e_1_2_5_50_1 Trost B (e_1_2_5_173_1) 2007 |
References_xml | – volume: 25 start-page: 947 year: 1986 end-page: 959 article-title: Selective synthesis by use of Lewis acids in the presence of organocopper and related reagents. New synthetic methods (61) publication-title: Angew Chem Int Ed Engl – volume: 31 start-page: 288 year: 1992 end-page: 290 article-title: Sugars as chiral auxiliaries for the synthesis of enantiomerically pure compounds publication-title: Angew Chem Int Ed Engl – volume: 15 start-page: 280 issue: 5 year: 2004 end-page: 294 article-title: A comprehensive review and evaluation of the side effects of the tumor necrosis factor alpha blockers etanercept, infliximab and adalimumab publication-title: J Dermatolog Treat – volume: 2 start-page: 123 year: 2000 end-page: 125 article-title: A short and efficient stereoselective synthesis of the polyhydroxylated macrolactone (+)‐aspicilin publication-title: Org Lett – volume: 20 start-page: 597 year: 2003 end-page: 630 article-title: Latanoprost publication-title: Drugs Aging – volume: 55 start-page: 173 issue: 1 year: 1990 end-page: 181 article-title: Acyclic stereoselection. 48. Reversal of stereochemistry in the aldol reactions of a chiral boron enolate publication-title: J Org Chem – volume: 29 start-page: 4397 year: 1988 end-page: 4400 article-title: Reversal of asymmetric induction in stereoselective Strecker synthesis on galactosyl amine as the chiral matrix publication-title: Tetrahedron Lett – year: 2005 – volume: 8 start-page: 2162 year: 2010 end-page: 2174 article-title: Bromopyrrole alkaloids as lead compounds against protozoan parasites publication-title: Mar Drugs – volume: 28 start-page: 1067 year: 1989 end-page: 1068 article-title: Carbohydrates as chiral templates: stereoselective tandem Mannich‐Michael reactions for the synthesis of piperidine alkaloids publication-title: Angew Chem Int Ed Engl – volume: 70 start-page: 2207 issue: 13 year: 2014 end-page: 2236 article-title: Methods for direct generation of α‐alkyl‐substituted aldehydes publication-title: Tetrahedron – volume: 75 start-page: 68 year: 1997 end-page: 73 article-title: Use of aldolases in the synthesis of non‐carbohydrate natural products. Stereoselective synthesis of aspicilin C3‐C9 fragment publication-title: Can J Chem – volume: 1990 start-page: 51 issue: 01 year: 1990 end-page: 52 article-title: Carbohydrates as chiral templates: stereoselective synthesis of chiral homoallyl amines and β‐amino acids publication-title: Synlett – volume: 14 start-page: 61 year: 2017 end-page: 111 article-title: Recent advances in the applications of SAMP/RAMP as chiral auxiliares in asymmetric synthesis publication-title: Curr Org Synth – volume: 290/62 start-page: 441 issue: 10 year: 1957 end-page: 448 article-title: Alkaloids of publication-title: Arch Pharm Ber Dtsch Pharm Ges – volume: 1991 start-page: 1039 issue: 11 year: 1991 end-page: 1042 article-title: Stereoselective synthesis of ‐amino acids via Strecker and Ugi reactions on carbohydrate templates publication-title: Synthesis – volume: 62 start-page: 1241 issue: 7 year: 1990 end-page: 1250 article-title: Camphor as a natural source of chirality in asymmetric synthesis publication-title: Pure Appl Chem – volume: 22 start-page: 787 issue: 7 year: 2011 end-page: 790 article-title: Total synthesis of (5 )‐dihydroyashabushiketol publication-title: Tetrahedron: Asymmetry – volume: 26 start-page: 63 year: 2006 end-page: 66 article-title: Use of prostaglandin (PGF α) to induce oestrus in postpartum Sahiwal cows publication-title: Pakistan Vet J – volume: 82 start-page: 2414 issue: 5 year: 2017 end-page: 2435 article-title: Total synthesis of reported structure of baulamycin A and its congeners publication-title: J Org Chem – volume: 15 start-page: 549 issue: 9 year: 1976 end-page: 551 article-title: Asymmetric synthesis of α‐substituted ketones by metalation, and alkylation of chiral hydrazones publication-title: Angew Chem Int Engl Ed – volume: 17 start-page: 3 issue: 1 year: 1976 end-page: 6 article-title: Applications of , ‐dimethylhydrazones to synthesis. Use in efficient, positionally, and stereochemically selective C=C bond formation; oxidative hydrolysis to carbonyl compounds publication-title: Tetrahedron Lett – volume: 47 start-page: 5595 year: 2006 end-page: 5597 article-title: Stereoselective total synthesis of (+)‐aspicilin publication-title: Tetrahedron Lett – volume: 123 start-page: 4480 year: 2001 end-page: 4491 article-title: Enantioselective and diastereoselective Mukaiyama‐Michael reactions catalyzed by bi(oxazoline)copper (II) complexes publication-title: J Am Chem Soc – volume: 63 start-page: 12845 issue: 52 year: 2007 end-page: 12852 article-title: Convenient synthesis of taranabant (MK‐0364), a novel cannabinoid‐1 receptor inverse agonist as an anti‐obesity agent publication-title: Tetrahedron – volume: 17 start-page: 2685 year: 2011 end-page: 2708 article-title: More than just sweet–sugar derived stereodifferentiating agents for asymmetric synthesis publication-title: Synthesis – volume: 127 start-page: 2023 issue: 11 year: 2015 end-page: 2028 article-title: A facile and efficient synthesis of (15 )‐latanoprost from chiral precursor Corey lactone diol publication-title: J Chem Sci – volume: 29 start-page: 5885 issue: 46 year: 1988 end-page: 5888 article-title: Enantioselective synthesis and absolute configuration of (−)‐pulo'upone by asymmetric intramolecular Diels‐Alder reaction publication-title: Tetrahedron Lett – volume: 20 start-page: 1 issue: 1 year: 2003 end-page: 48 article-title: Marine natural products publication-title: Nat Prod Rep – volume: 8 start-page: 4299 year: 2006 end-page: 4302 article-title: Understanding the origins of remote asymmetric induction in the boron aldol reactions of β‐alkoxy methyl ketones publication-title: Org Lett – volume: 10 start-page: 4233 year: 1969 end-page: 4236 article-title: Asymmetric synthesis with amino acid I asymmetric induction in the alkylation of keto‐enamine publication-title: Tetrahedron Lett – volume: 67 start-page: 1262 issue: 8 year: 2004 end-page: 1267 article-title: Nagelamides A‐H, new dimeric bromopyrrole alkaloids from marine sponge species publication-title: J Nat Prod – volume: 125 start-page: 14666 issue: 48 year: 2003 end-page: 14667 article-title: Determining the solution state orientation of Ti enolate via stable isotope labeling, NMR spectroscopy, and modeling studies publication-title: J Am Chem Soc – volume: 38 start-page: 6011 issue: 34 year: 1997 end-page: 6014 article-title: Synthesis of the C1‐C16 fragment of the marine toxin, laulimalide publication-title: Tetrahedron Lett – volume: 5 start-page: 1195 year: 1994 end-page: 1198 article-title: Asymmetric Michael addition of thiols to (1 ,2 ,4 )‐(−)‐2,10‐ ‐enoylcamphorsultam publication-title: Temhedmn: Asy‐Ry – volume: 121 start-page: 7559 issue: 33 year: 1999 end-page: 7573 article-title: Chiral bis(oxazoline)copper (II) complexes as Lewis acid catalysts for the enantioselective Diels‐Alder reaction publication-title: J Am Chem Soc – volume: 53 start-page: 14823 issue: 44 year: 1997 end-page: 14870 article-title: Synthetic studies with carbohydrate‐derived chiral auxiliaries publication-title: Tetrahedron – volume: 56 start-page: 4405 issue: 26 year: 2000 end-page: 4413 article-title: Asymmetric desymmetrization of a σ‐symmetric erythritol derivative using C2‐symmetric bis‐sulfoxide: a total synthesis of (+)‐aspicilin publication-title: Tetrahedron – volume: 14 start-page: 5752 issue: 22 year: 2012 end-page: 5755 article-title: Noninnocent role of ‐methyl pyrrolidinone in thiazolidinethione‐promoted asymmetric aldol reactions publication-title: Org Lett – volume: 138 start-page: 345 issue: 1 year: 2016 end-page: 355 article-title: Structure‐reactivity relationships in lithiated Evans enolates: influence of aggregation and solvatation on the stereochemistry and mechanism of aldol additions publication-title: J Am Chem Soc – volume: 11 start-page: 1833 issue: 8 year: 2009 end-page: 1836 article-title: Synthetic studies on daphicyclidin A: enantiocontrolled construction of the BCD ring system publication-title: Org Lett – volume: 53 start-page: 3250 issue: 26 year: 2012 end-page: 3253 article-title: Efficient total synthesis of manzacidin B publication-title: Tetrahedron Lett – start-page: 375 year: 1993 end-page: 382 – volume: 1 start-page: 1 year: 2002 end-page: 21 article-title: Stoichiometric asymmetric processes publication-title: J Chem Soc, Perkin Trans – volume: 26 start-page: 511 issue: 4 year: 1985 end-page: 514 article-title: Structure of swinholide A, a new macrolide from the marine sponge publication-title: Tetrahedron Lett – volume: 14 start-page: 1053 year: 1987 end-page: 1054 article-title: Secondary Mannich bases via trimethylsilyl trifluoromethanesulphonate promoted addition of silyl enol ethers to Schiff bases publication-title: J Chem Soc Chem Commun – volume: 77 start-page: 1765 year: 2012 end-page: 1288 article-title: The role of β‐bulky substituents in aldol reactions of boron enolates of methylketones with aldehydes: experimental and theoretical studies by DFT analysis publication-title: J Org Chem – volume: 13 start-page: 8648 issue: 31 year: 2007 end-page: 8659 article-title: Carbohydrates as synthetic tools in organic chemistry publication-title: Chem A Eur J – volume: 19 start-page: 7429 issue: 6 year: 2014 end-page: 7439 article-title: Easy access to Evans oxazolidinones. Stereoselective synthesis and antibacterial activity of a new 2‐oxazolidinone derivative publication-title: Molecules – volume: 12 start-page: 1133 year: 1971 end-page: 1136 article-title: Total synthesis of (+)‐mesembrine by asymmetric synthesis with amino acid publication-title: Tetrahedron Lett – volume: 65 start-page: 8714 issue: 42 year: 2009 end-page: 8721 article-title: Addition of kinetic boron enolates generated from β‐alkoxy methyl ketones to aldehydes. Density functional theory calculations on the transition structures publication-title: Tetrahedron – volume: 118 start-page: 3059 year: 1996 end-page: 3060 article-title: Total synthesis of swinholide A publication-title: J Am Chem Soc – volume: 39 start-page: 5597 issue: 31 year: 1998 end-page: 5600 article-title: Concise enantioselective synthesis of (+)‐aspicilin based on a ruthenium catalyzed olefin metathesis reaction publication-title: Tetrahedron Lett – volume: 19 start-page: 4648 issue: 17 year: 2017 end-page: 4651 article-title: Construction of the [6,5,7,5] tetracyclic core of calyciphylline A type alkaloids via a tandem semipinacol rearrangement/Nicholas reaction publication-title: Org Lett – start-page: 234 year: 2007 end-page: 238 – volume: 29 start-page: 1441 year: 2018 end-page: 1446 article-title: Synthesis of a chiral auxiliary family from levoglucosenone and evaluation in the Diels‐Alder reaction publication-title: Synlett – volume: 81 start-page: 3890 year: 2016 end-page: 3900 article-title: Stereoselective α‐hydroxylation of amides using Oppolzer's sultam as chiral auxiliary publication-title: J Org Chem – volume: 2 start-page: 137 year: 2014 end-page: 146 article-title: The SAMP‐/RAMP‐hydrazone methodology in asymmetric synthesis of 4 ‐ferrugineone and 4 ,5 ‐ferrugineol: the pheromones of palm weevils publication-title: Iran Chem Commun – volume: 49 start-page: 4289 issue: 27 year: 2008 end-page: 4291 article-title: Enantioselective total synthesis of ( )‐(−)‐quinolactacin B publication-title: Tetrahedron Lett – volume: 51 start-page: 1 year: 1997 end-page: 200 article-title: Asymmetric aldol reactions using boron enolates publication-title: Org React – volume: 141 start-page: 388 issue: 1 year: 2019 end-page: 401 article-title: Structures and reactivities of sodiated Evans enolates: role of solvatation and mixed aggregation on the stereochemistry and mechanism of alkylations publication-title: J Am Chem Soc – volume: 3 start-page: 23105 year: 2013 end-page: 23118 article-title: Diastereoselective 1,3‐dipolar cycloadditions of both electronically modified phenyl‐nitrile oxides and stilbenes publication-title: RSC Adv – volume: 36 start-page: 1315 year: 2005 end-page: 1392 article-title: Recent advances in catalytic asymmetric addition to imines and related C=N systems publication-title: Chem Inform – volume: 39 start-page: 565 issue: 6 year: 2013 end-page: 586 article-title: Microbial metabolites inhibiting sterol biosynthesis: their chemical diversity and characteristics of the mechanism of action publication-title: Russ J Bioorganic Chem – volume: 36 start-page: 6527 year: 1995 end-page: 6530 article-title: Reversal of π‐face selectivity in the Evans aldol reaction with fluoral: a computational study on the transition states using semiempirical calculations publication-title: Tetrahedron Lett – volume: 44 start-page: 5487 year: 1988 end-page: 5494 article-title: Carbohydrates as chiral templates: asymmetric Ugi‐synthesis of α‐amino acids using galactosylamines as the chiral matrices publication-title: Tetrahedron – volume: 2012 start-page: 1819 issue: 9 year: 2012 end-page: 1824 article-title: Total synthesis of (+)‐aspicilin by an alkyne‐based approach and its biological evaluation publication-title: Eur J Org Chem – volume: 37 start-page: 1044 issue: 8 year: 1998 end-page: 1070 article-title: Modern variants of the Mannich reaction publication-title: Angew Chem Int Ed Engl – volume: 47 start-page: 2299 issue: 15 year: 2015 end-page: 2316 article-title: Stereoselective total synthesis of the diastereomeric tricyclic alkaloids tetraponerine‐7 and tetraponerine‐8 using ‐pivaloyled ‐arabinopyranosylamine as the common auxiliary publication-title: Synthesis – volume: 60 start-page: 1273 issue: 4 year: 1977 end-page: 1295 article-title: Stereoselektivität und reaktivität bei der 1,3‐dipolaren cycloaddition chiraler ‐(alkoxyalkyl)nitrone publication-title: Helv Chim Acta – volume: 112 start-page: 3710 year: 1990 end-page: 3712 article-title: Absolute stereostructure of swinholide A, a potent cytotoxic macrolide from the Okinawan marine sponge publication-title: J Am Chem Soc – volume: 20 start-page: 3053 year: 2018 end-page: 3056 article-title: Stereocontrolled construction of ABCD tetracyclic ring system with vicinal all‐carbon quaternary stereogenic centers of calyciphylline A type alkaloids publication-title: Org Lett – volume: 91 start-page: 5675 issue: 20 year: 1969 end-page: 5677 article-title: Stereo‐controlled synthesis of dl‐prostaglandins F α and E2 publication-title: J Am Chem Soc – volume: 116 start-page: 9391 issue: 20 year: 1994 end-page: 9392 article-title: Total synthesis of swinholide A and hemiswinholide A publication-title: J Am Chem Soc – volume: 69 start-page: 1092 year: 2013 end-page: 1104 article-title: Synthesis of spiroindoline phytoalexin ( )‐(−)‐spirobrassinin and its unnatural ( )‐(+)‐enantiomer publication-title: Tetrahedron – volume: 6 start-page: 30498 year: 2016 end-page: 30551 article-title: Applications of oxazolidinones as chiral auxiliaries in the asymmetric alkylation reaction applied to total synthesis publication-title: RSC Adv – volume: 36 start-page: 2607 year: 1995 end-page: 2610 article-title: Total synthesis of the macrolide (+)‐aspicilin by an asymmetric catalyzed macrocyclization of an ω‐alkynal ester publication-title: Tetrahedron Lett – volume: 489 start-page: 278 issue: 7415 year: 2012 end-page: 281 article-title: Stereocontrolled organocatalytic synthesis of prostaglandin PGF α in seven steps publication-title: Nature – volume: 124 start-page: 10759 issue: 36 year: 2002 end-page: 10764 article-title: Mechanism of the double aldol reaction: the first spectroscopic characterization of a carbon‐bound boron enolate derived from carboxylic esters publication-title: J Am Chem Soc – volume: 1 start-page: 467 year: 1995 end-page: 494 article-title: Synthesis of zaragozic acid A/squalestatin S1 publication-title: Chem A Eur J – volume: 129 start-page: 4981 issue: 16 year: 2007 end-page: 4991 article-title: BH ‐catalyzed oligomerization of ethyl diaxoacetate: the role of C‐boron enolates publication-title: J Am Chem Soc – volume: 137 start-page: 1124 year: 2011 end-page: 1129 article-title: Pharmacological actions of the South African medicinal and functional food plant and its principal alkaloids publication-title: J Ethnopharmacol – volume: 29 start-page: 998 year: 2018 end-page: 1031 article-title: Natural products from marine invertebrates and microorganisms in Brazil between 2004 and 2017: still the challenges, more rewards publication-title: J Braz Chem Soc – volume: 75 start-page: 8578 issue: 24 year: 2010 end-page: 8584 article-title: Origins of stereoselectivity in the α‐alkylation of chiral hydrazones publication-title: J Org Chem – volume: 62 start-page: 377 issue: 2 year: 1997 end-page: 386 article-title: Total synthesis of (+)‐aspicilin. The naked carbon skeleton strategy vs the bioorganic approach publication-title: J Org Chem – volume: 122 start-page: 10708 issue: 43 year: 2000 end-page: 10709 article-title: Total synthesis and absolute structure of manzacidin A and C publication-title: J Am Chem Soc – volume: 12 start-page: 3362 issue: 21 year: 2014 end-page: 3365 article-title: Diastereoselective formation of aziridines from diazocarbonyl compounds and ‐( ‐pivaloylated ‐galactosyl)benzylideneamines and ring‐opening reactions with ‐toluenethiol publication-title: Org Biomol Chem – volume: 115 start-page: 1308 issue: 7 year: 2014 end-page: 1321 article-title: Prostaglandin F α inhibits adipogenesis via an autocrine‐mediated interleukin‐11/glycoprotein 130/STAT1‐dependent signaling cascade publication-title: J Cell Biochem – volume: 97 start-page: 6908 year: 1975 end-page: 6909 article-title: Preparation of an optically active prostaglandin intermediate via asymmetric induction publication-title: J Am Chem Soc – volume: 93 start-page: 2325 issue: 9 year: 1971 end-page: 2327 article-title: Plant antitumor agents. VI. The isolation and structure of taxol, a novel antileukemic and antitumor agent from publication-title: J Am Chem Soc – volume: 355 start-page: 303 year: 2013 end-page: 307 article-title: Diastereoselective Povarov‐like reaction involving ‐pivaloylated ‐galactosylimine publication-title: Adv Synth Catal – volume: 63 start-page: 7505 issue: 21 year: 1998 end-page: 7515 article-title: Efficient conditions for conversion of 2‐ substituted furans into 4‐oxygenated 2‐enoic acids and its application to synthesis of (+)‐aspicilin, (+)‐patulolide A, and (−)‐pyrenophorin publication-title: J Org Chem – volume: 12 start-page: 2868 issue: 12 year: 2010 end-page: 2871 article-title: The pivotal role of chelation as a stereochemical control element in non‐Evans aldol product formation publication-title: Org Lett – volume: 125 start-page: 13531 issue: 44 year: 2003 end-page: 13540 article-title: A cycloaddition cascade approach to the total synthesis of (−)‐FR182877 publication-title: J Am Chem Soc – volume: 385 start-page: 1295 issue: 9975 year: 2015 end-page: 1304 article-title: Latanoprost for open‐angle glaucoma (UKGTS): a randomized, multicenter, placebo‐controlled trial publication-title: The Lancet – volume: 56 start-page: 917 year: 2000 end-page: 947 article-title: Advances in asymmetric enolate methodology publication-title: Tetrahedron – volume: 48 start-page: 2228 year: 2009 end-page: 2230 article-title: Stereoselective synthesis of enantiomerically pure nupharamine alkaloids from castoreum publication-title: Angew Chem Int Ed Engl – volume: 66 start-page: 3940 year: 2001 end-page: 3947 article-title: Synthesis, absolute configuration, and enantiomeric enrichment of a cruciferous oxindole phytoalexin, ( )‐(−)‐spirobrassinin, and its oxazoline analog publication-title: J Org Chem – year: 2013 – volume: 112 start-page: 7001 issue: 19 year: 1990 end-page: 7031 article-title: Total synthesis of the macrolide antibiotic cytovaricin publication-title: J Am Chem Soc – volume: 36 start-page: 5773 issue: 32 year: 1995 end-page: 5776 article-title: One‐pot synthesis of β‐amino esters from aldehydes using lanthanide triflate as a catalyst publication-title: Tetrahedron Lett – volume: 87 start-page: 1 year: 2012 end-page: 14 article-title: Intraluteal prostaglandin biosynthesis and signaling are selectively directed towards PGF α during luteolysis but towards PGE during the establishment of pregnancy in sheep publication-title: Biol Reprod – volume: 43 start-page: 9489 year: 2002 end-page: 9492 article-title: Spirocyclization strategy toward indole phytoalexins. The first synthesis of (±)‐1‐methoxyspirobrassinin, (±)‐1‐methoxyspirobrassinol, and (±)‐1‐methoxyspirobrassinol methyl ether publication-title: Tetrahedron Lett – year: 2009 – volume: 48 start-page: 1657 issue: 13 year: 2018 end-page: 1662 article-title: Alternative total synthesis of (+)‐aspicilin publication-title: Synth Commun – volume: 14 start-page: 466 issue: 2 year: 2010 end-page: 469 article-title: In situ FTIR study and scale‐up of an enolization‐azidation sequence publication-title: Org Process Res Dev – volume: 25 start-page: 35 issue: 1 year: 2008 end-page: 94 article-title: Marine natural products publication-title: Nat Prod Rep – volume: 8 start-page: 1739 issue: 18 year: 2008 end-page: 1761 article-title: Amino sugars and glycosylamines as tools in stereoselective synthesis publication-title: Curr Org Chem – volume: 50 start-page: 119 issue: 3 year: 1996 end-page: 130 article-title: Psychoactive constituents of the genus N.E.Br. and other Mesembryanthemaceae: a review publication-title: J Ethnopharmacol – volume: 115 start-page: 4497 year: 1993 end-page: 4513 article-title: Total synthesis of (+)‐A83543A [(+)‐lepicidin A] publication-title: J Am Chem Soc – volume: 68 start-page: 4830 issue: 24 year: 2012 end-page: 4837 article-title: Asymmetric aza‐Friedel–Crafts reaction of indoles induced by ‐pivaloylated ‐galactosylamine as the chiral auxiliary publication-title: Tetrahedron – volume: 19 start-page: 1 issue: 1 year: 2002 end-page: 48 article-title: Marine natural products publication-title: Nat Prod Rep – volume: 58 start-page: 5573 year: 2002 end-page: 5590 article-title: Proline‐catalyzed asymmetric reactions publication-title: Tetrahedron – volume: 4 start-page: 823 year: 1994 end-page: 826 article-title: Enantioselective synthesis of PD144723: a potent stereospecific anticonvulsant publication-title: Bioorg Med Chem Lett – volume: 5 start-page: 381 year: 1973 end-page: 384 article-title: A biogenetic‐type asymmetric cyclization syntheses of optically active α‐cyclocitral and ‐α‐damascone publication-title: Tetrahedron Lett – start-page: 1363 issue: 13 year: 2007 end-page: 1365 article-title: Reversibility in the boron‐mediated ketone‐ketone aldol reaction publication-title: J Chem Commun – year: 2018 – volume: 1991 start-page: 649 year: 2010 end-page: 654 article-title: Carbohydrates as chiral templates: stereoselective Strecker synthesis of ‐α‐amino nitriles and acids using ‐pivaloylated ‐galactosylamine as the auxiliary publication-title: Eur J Org Chem – start-page: 1151 issue: 9 year: 1994 end-page: 1152 article-title: Stereoselective construction of the C18‐C32 fragment of swinholide A publication-title: J Chem Soc Chem Commun – volume: 10 start-page: 4237 issue: 48 year: 1969 end-page: 4240 article-title: Asymmetric synthesis with amino acid II asymmetric synthesis of optically active 4,4‐disubstituted‐cyclohexenone publication-title: Tetrahedron Lett – volume: 65 start-page: 5031 issue: 16 year: 2000 end-page: 5033 article-title: Solution structure of a chiral dialkylboron enolate by NMR spectroscopy and simulated annealing: unusual stabilization of this intermediate by a boron‐nitrogen interaction publication-title: J Org Chem – volume: 49 start-page: 7426 issue: 52 year: 2008 end-page: 7429 article-title: Short and stereoselective synthesis of manzacidins A and C, and their enantiomers publication-title: Tetrahedron Lett – volume: 1997 start-page: 1151 issue: 10 year: 1997 end-page: 1160 article-title: Enantioselective syntheses of 2‐alkyl‐, 2,6‐dialkylpiperidines and indolizidine alkaloids through diastereoselective Mannich‐Michael reactions publication-title: Synthesis – start-page: 1267 year: 1970 end-page: 1271 article-title: Absolute configuration of mesembrine and related alkaloids: X‐ray analysis of 6‐epimesembranol methiodide publication-title: J Chem Soc B: Phisical Organic – volume: 2 start-page: 3583 issue: 23 year: 2000 end-page: 3586 article-title: Chemoenzymatic synthesis of (+)‐aspicilin from chlorobenzene publication-title: Org Lett – volume: 304 year: 1994 – volume: 109 start-page: 7534 issue: 24 year: 1987 end-page: 7536 article-title: Total synthesis of a C15 ginkgolide, (±)‐bilobalide publication-title: J Am Chem Soc – volume: 53 start-page: 7127 year: 1997 end-page: 7138 article-title: Asymmetric synthesis of a taxol C‐ring by aldol condensation and radical cyclization publication-title: Tetrahedron – volume: 56 start-page: 4574 year: 1991 end-page: 4576 article-title: Manzacidins A‐C, novel tetrahydropyrimidine alkaloids from the okinawan marine sponge sp publication-title: J Org Chem – volume: 49 start-page: 202 year: 2017 end-page: 208 article-title: Hydroxyl‐assisted ‐reduction of 1,3‐enynes: application to the formal synthesis of (+)‐aspicilin publication-title: Synthesis – volume: 17 start-page: 13330 year: 2012 end-page: 13344 article-title: Asymmetric construction of all‐carbon quaternary stereocenters by chiral‐auxiliary‐mediated Claisen rearrangement and total synthesis of (+)‐bakuchiol publication-title: Molecules – year: 2004 – volume: 38 start-page: 2859 year: 1997 end-page: 2860 article-title: Callystatin A, a potent cytotoxic polyketide from the marine sponge, publication-title: Tetrahedron Lett – start-page: 273 year: 1993 – volume: 140 start-page: 3077 issue: 8 year: 2018 end-page: 3090 article-title: Lithium amino alkoxide‐Evans enolate mixed aggregates: aldol addition with matched and mismatched stereocontrol publication-title: J Am Chem Soc – volume: 41 start-page: 587 issue: 5 year: 2000 end-page: 590 article-title: Total synthesis of (−)‐eburnamonine and (+)‐ ‐eburnamonine from a chiral non‐racemic 4,4‐disubstituted γ‐lactone publication-title: Tetrahedron Lett – volume: 8 start-page: 1279 year: 2011 end-page: 1282 article-title: A concise stereoselective total synthesis of synargentolide A from 3,4,6‐tri‐ ‐acetyl‐ ‐glucal publication-title: Synthesis – volume: 15 start-page: 113 year: 1998 end-page: 158 article-title: Marine natural products publication-title: Nat Prod Rep – volume: 20 start-page: 1215 year: 2010 end-page: 1231 article-title: Statins and the squalene synthase inhibitor zaragozic acid stimulate the non‐amyloidogenic pathway of amyloid‐β protein precursor processing by suppression of cholesterol synthesis publication-title: J Alzheimers Dis – volume: 49 start-page: 1989 year: 1989 article-title: ChemInform abstract: design and implementation of tactically novel strategies for stereochemical control using the chiron approach publication-title: Chem Inform – volume: 96 start-page: 7807 issue: 25 year: 1974 end-page: 7808 article-title: Useful diene for the Diels‐Alder reaction publication-title: J Am Chem Soc – volume: 20 start-page: 657 issue: 6 year: 1997 end-page: 663 article-title: Os fármacos e a quiralidade: uma breve abordagem publication-title: Quim Nova – year: 1983 – volume: 110 start-page: 651 year: 1988 end-page: 652 article-title: Asymmetric synthesis on carbohydrate templates: stereoselective Ugi‐synthesis of α‐amino acid derivatives publication-title: J Am Chem Soc – volume: 82 start-page: 7595 year: 2017 end-page: 7601 article-title: Evans enolates: structures and mechanisms underlying the aldol addition of oxazolidinone‐derived boron enolates publication-title: J Am Chem Soc – volume: 103 start-page: 3099 year: 1981 end-page: 3111 article-title: Stereoselective aldol reactions condensations via boron enolates publication-title: J Am Chem Soc – volume: 8 start-page: 4272 year: 2002 end-page: 4284 article-title: Asymmetric total synthesis of (−)‐callystatin A and (−)‐20‐ ‐callystatin A employing chemical and biological methods publication-title: Chem A Eur J – volume: 250 start-page: 647 issue: 1 year: 1912 end-page: 667 article-title: Ueber ein kondensationsprodukt aus formaldehyd, ammoniak und antipyrin publication-title: Arch Pharm – volume: 67 start-page: 1627 year: 1995 end-page: 1635 article-title: Stereoselective syntheses using carbohydrates as chiral auxiliaries publication-title: Pure Appl Chem – volume: 58 start-page: 2253 issue: 12 year: 2002 end-page: 2329 article-title: The SAMP/RAMP‐hydrazone methodology in asymmetric synthesis publication-title: Tetrahedron – start-page: 3 year: 2007 end-page: 9 – volume: 21 start-page: 312 year: 1998 end-page: 318 article-title: Abordagens em síntese assimétrica publication-title: Quim Nova – start-page: 271 year: 2007 end-page: 146 – volume: 15 start-page: 6281 year: 2017 end-page: 6301 article-title: Recent advances in asymmetric total synthesis of prostaglandins publication-title: Org Biomol Chem – volume: 100 start-page: 4267 issue: 12 year: 2000 end-page: 4282 article-title: Toward a carbohydrate‐based chemistry: progress in the development of general‐purpose chiral synthons from carbohydrates publication-title: Chem Rev – volume: 73 start-page: 6443 year: 2017 end-page: 6447 article-title: Chiron approach for the total synthesis of (+)‐synargentolide B publication-title: Tetrahedron – volume: 98 start-page: 465 year: 2017 end-page: 479 article-title: Mechanisms for rescue of corpus luteum during pregnancy: gene expression in bovine corpus luteum following intrauterine pulses of prostaglandins E and F α publication-title: Biol Reprod – volume: 132 start-page: 12319 year: 2010 end-page: 12330 article-title: Transition state models for probing stereoinduction in Evans chiral auxiliary‐based asymmetric aldol reactions publication-title: J Am Chem Soc – volume: 35 start-page: 6883 issue: 37 year: 1994 end-page: 6886 article-title: TMSO‐triflate‐assisted addition of enols to heteroaromatic imines or hydroxyaminal intermediates publication-title: Tetrahedron Lett – volume: 45 start-page: 959 year: 2013 end-page: 965 article-title: Asymmetric synthesis of synargentolide A and its 3‐epimer using the RAMP‐hydrazone methodology publication-title: Synthesis – volume: 43 start-page: 2223 issue: 7 year: 1970 end-page: 2229 article-title: Chemical constituents of A (Betulaceae). I. Phenyl propane derivatives isolated from publication-title: Bull Chem Soc Jpn – start-page: 355 year: 2007 – volume: 52 start-page: 2080 issue: 17 year: 2011 end-page: 2084 article-title: Enantioselective formal total synthesis of the dendrobatidae frog toxin, (+)‐pumiliotoxin B, via ‐directed alkyne free radical hydrostannation publication-title: Tetrahedron Lett – volume: 10 start-page: 4851 year: 2012 end-page: 4863 article-title: Proline sulfonamide‐catalyzed Yamada‐Otoni condensation: reaction development, substrate scope and scaffold reactivity publication-title: Org Biomol Chem – volume: 67 start-page: 6753 issue: 35 year: 2011 end-page: 6761 article-title: Enantioselective syntheses of the assigned structures of the helibisabonols A and B publication-title: Tetrahedron – volume: 73 start-page: 1253 issue: 4 year: 2008 end-page: 1263 article-title: 1,5‐Anti stereocontrol in the boron‐mediated aldol reactions of β‐alkoxy methyl ketones: the role of the formyl hydrogen bond publication-title: J Org Chem – volume: 32 start-page: 336 issue: 3 year: 1993 end-page: 358 article-title: Carbohydrates as chiral auxiliaries in stereoselective synthesis. New synthetic methods publication-title: Angew Chem Int Ed Engl – volume: 26 start-page: 5834 year: 2007 end-page: 5839 article-title: Synthesis and structural characterization of the bis(diisopropylamino)boron enolate of ‐butyl methyl ketone publication-title: Organometallics – volume: 26 start-page: 557 year: 1987 end-page: 559 article-title: Diastereoselective Strecker synthesis of α‐aminonitriles on carbohydrate templates publication-title: Angew Chem Int Ed Engl – volume: 41 start-page: 1650 issue: 10 year: 2002 end-page: 1667 article-title: Catalytic enantioselective Diels–Alder reactions: methods, mechanistic fundamentals, pathways, and applications publication-title: Angew Chem Int Ed Engl – volume: 1995 start-page: 1185 issue: 7 year: 1995 end-page: 1191 article-title: Diastereo‐ and enantioselective synthesis of the 18‐membered lichen macrolide (+)‐aspicilin publication-title: Liebigs Ann – volume: 47 start-page: 6079 issue: 32 year: 1991 end-page: 6111 article-title: Asymmetric synthesis of α‐amino acids from carbohydrates as chiral templates publication-title: Tetrahedron – volume: 137 start-page: 13087 issue: 40 year: 2015 end-page: 13095 article-title: Evans enolates: solution structures of lithiated oxazolidinone‐derived enolates publication-title: J Am Chem Soc – volume: 17 start-page: 1177 issue: 2 year: 2012 end-page: 1190 article-title: Mild and efficient Winterfeldt oxidation of 1,2,3,4‐tetrahydro‐γ‐carbolines for the synthesis of dihydropyrrolo[3,2‐ ]‐quinolones and pyrrolo[3,2‐ ]quinolones publication-title: Molecules – volume: 32 start-page: 7397 issue: 50 year: 1991 end-page: 7400 article-title: Substantial refinement of the photochemical synthesis of (+)‐aspicilin publication-title: Tetrahedron Lett – volume: 29 start-page: 3423 issue: 28 year: 1988 end-page: 3426 article-title: Enantioselective total synthesis of bilobalide, a C15 ginkgolide publication-title: Tetrahedron Lett – volume: 57 start-page: 9117 issue: 29 year: 2018 end-page: 9121 article-title: Enantioselective synthesis of (−)‐halenaquinone publication-title: Angew Chem Int Ed – volume: 53 start-page: 123 issue: 2 year: 2000 end-page: 130 article-title: A new antimitotic substance, FR182877 publication-title: J Antibiot – ident: e_1_2_5_122_1 doi: 10.1351/pac199062071241 – ident: e_1_2_5_33_1 doi: 10.1007/s12039-015-0963-2 – ident: e_1_2_5_117_1 doi: 10.1016/S0040-4020(97)00412-2 – ident: e_1_2_5_46_1 doi: 10.1016/0040-4039(88)85179-7 – ident: e_1_2_5_87_1 doi: 10.1021/ol302761n – volume-title: The Chemistry of Metal Enolates year: 2009 ident: e_1_2_5_96_1 contributor: fullname: Domingo LR – volume: 82 start-page: 7595 year: 2017 ident: e_1_2_5_107_1 article-title: Evans enolates: structures and mechanisms underlying the aldol addition of oxazolidinone‐derived boron enolates publication-title: J Am Chem Soc contributor: fullname: Zhang Z – ident: e_1_2_5_133_1 doi: 10.3390/md8072162 – volume-title: Topics in Heterocyclic Chemistry year: 2018 ident: e_1_2_5_5_1 contributor: fullname: Srivastava A – ident: e_1_2_5_95_1 doi: 10.1021/ol061671q – ident: e_1_2_5_120_1 doi: 10.1016/S0040-4039(97)01336-1 – ident: e_1_2_5_147_1 doi: 10.1002/chem.200701010 – ident: e_1_2_5_105_1 doi: 10.1021/ja010302g – ident: e_1_2_5_109_1 doi: 10.1021/jacs.8b10364 – ident: e_1_2_5_132_1 doi: 10.1021/jo00014a052 – volume: 49 start-page: 1989 year: 1989 ident: e_1_2_5_156_1 article-title: ChemInform abstract: design and implementation of tactically novel strategies for stereochemical control using the chiron approach publication-title: Chem Inform contributor: fullname: Hanessian S – ident: e_1_2_5_171_1 doi: 10.1002/ardp.19122500151 – ident: e_1_2_5_43_1 doi: 10.1016/j.tet.2012.11.067 – ident: e_1_2_5_121_1 doi: 10.1016/S0040-4039(99)02131-0 – ident: e_1_2_5_6_1 doi: 10.1590/S0100-40421997000600015 – ident: e_1_2_5_25_1 doi: 10.1002/1521-3773(20020517)41:10<1650::AID-ANIE1650>3.0.CO;2-B – ident: e_1_2_5_161_1 doi: 10.1002/anie.198910671 – ident: e_1_2_5_178_1 doi: 10.1039/c39870001053 – ident: e_1_2_5_123_1 doi: 10.1016/0957-4166(94)80155-X – ident: e_1_2_5_30_1 doi: 10.1002/jcb.24785 – ident: e_1_2_5_22_1 doi: 10.1002/anie.201805370 – ident: e_1_2_5_138_1 doi: 10.1039/b009029h – ident: e_1_2_5_153_1 doi: 10.2174/1385272043369485 – volume: 26 start-page: 63 year: 2006 ident: e_1_2_5_32_1 article-title: Use of prostaglandin (PGF2α) to induce oestrus in postpartum Sahiwal cows publication-title: Pakistan Vet J contributor: fullname: Amjad M – volume: 1 start-page: 1 year: 2002 ident: e_1_2_5_81_1 article-title: Stoichiometric asymmetric processes publication-title: J Chem Soc, Perkin Trans contributor: fullname: Jones S – ident: e_1_2_5_142_1 doi: 10.1002/anie.199303361 – volume-title: Strategic Applications of Named Reactions in Organic Synthesis year: 2005 ident: e_1_2_5_82_1 contributor: fullname: Kurti L – ident: e_1_2_5_14_1 doi: 10.1016/S0040-4020(02)00080-7 – ident: e_1_2_5_74_1 doi: 10.1139/v97-010 – volume: 36 start-page: 1315 year: 2005 ident: e_1_2_5_174_1 article-title: Recent advances in catalytic asymmetric addition to imines and related C=N systems publication-title: Chem Inform contributor: fullname: Vilaivan T – ident: e_1_2_5_176_1 doi: 10.1016/00404-0399(50)1096Z- – ident: e_1_2_5_160_1 doi: 10.1021/ja00832a031 – ident: e_1_2_5_23_1 doi: 10.1055/s-0037-1610148 – ident: e_1_2_5_61_1 doi: 10.1055/s-0030-1258458 – ident: e_1_2_5_85_1 doi: 10.1016/0040-4039(95)01312-6 – ident: e_1_2_5_27_1 doi: 10.1039/C7OB01341H – ident: e_1_2_5_76_1 doi: 10.1016/0040-4039(95)00351-C – ident: e_1_2_5_11_1 doi: 10.1016/S0040-4020(02)00516-1 – ident: e_1_2_5_180_1 doi: 10.1002/anie.200805606 – ident: e_1_2_5_175_1 doi: 10.1055/s-1990-20985 – ident: e_1_2_5_56_1 doi: 10.1021/ja00099a091 – ident: e_1_2_5_111_1 doi: 10.1002/9780470134979.ch16 – ident: e_1_2_5_48_1 doi: 10.1002/anie.197605492 – ident: e_1_2_5_73_1 doi: 10.1016/S0040-4039(98)01130-7 – ident: e_1_2_5_144_1 doi: 10.1002/9783527654543.ch1 – ident: e_1_2_5_63_1 doi: 10.1002/1521-3765(20020916)8:18<4272::AID-CHEM4272>3.0.CO;2-K – ident: e_1_2_5_114_1 doi: 10.7164/antibiotics.53.123 – ident: e_1_2_5_34_1 doi: 10.2165/00002512-200320080-00005 – ident: e_1_2_5_36_1 doi: 10.1016/j.tetlet.2008.04.130 – ident: e_1_2_5_100_1 doi: 10.1021/jo00288a029 – ident: e_1_2_5_80_1 doi: 10.3233/JAD-2010-091621 – ident: e_1_2_5_163_1 doi: 10.1002/(SICI)1521-3773(19980504)37:8<1044::AID-ANIE1044>3.0.CO;2-E – ident: e_1_2_5_79_1 doi: 10.1002/chem.19950010712 – ident: e_1_2_5_104_1 doi: 10.1021/op900299c – ident: e_1_2_5_83_1 doi: 10.1002/9783527619566 – ident: e_1_2_5_89_1 doi: 10.1021/om700676w – ident: e_1_2_5_91_1 doi: 10.1021/ja067264r – ident: e_1_2_5_94_1 doi: 10.1021/jo2023119 – ident: e_1_2_5_110_1 doi: 10.1016/S0960-894X(01)80855-6 – ident: e_1_2_5_10_1 doi: 10.1016/S0040-4020(99)00964-3 – ident: e_1_2_5_42_1 doi: 10.1021/ol9003405 – ident: e_1_2_5_166_1 doi: 10.1002/adsc.201200761 – ident: e_1_2_5_108_1 doi: 10.1021/jacs.7b13776 – ident: e_1_2_5_28_1 doi: 10.1093/biolre/iox183 – ident: e_1_2_5_179_1 doi: 10.1055/s-0034-1380215 – ident: e_1_2_5_75_1 doi: 10.1021/jo9614811 – ident: e_1_2_5_9_1 doi: 10.3390/molecules19067429 – ident: e_1_2_5_137_1 doi: 10.1039/b207130b – ident: e_1_2_5_135_1 doi: 10.1039/b701534h – ident: e_1_2_5_126_1 doi: 10.1016/j.tetlet.2010.10.141 – ident: e_1_2_5_41_1 doi: 10.1021/acs.orglett.7b02274 – ident: e_1_2_5_115_1 doi: 10.1021/ja037643 – ident: e_1_2_5_12_1 doi: 10.1016/S0040-4039(01)88662-7 – volume: 2 start-page: 137 year: 2014 ident: e_1_2_5_53_1 article-title: The SAMP‐/RAMP‐hydrazone methodology in asymmetric synthesis of 4S‐ferrugineone and 4S,5S‐ferrugineol: the pheromones of palm weevils publication-title: Iran Chem Commun contributor: fullname: Saeidian H – ident: e_1_2_5_58_1 doi: 10.1039/C39940001151 – ident: e_1_2_5_69_1 doi: 10.1021/ol006457v – ident: e_1_2_5_7_1 doi: 10.1590/S0100-40421998000300012 – ident: e_1_2_5_102_1 doi: 10.1021/ja00401a031 – volume-title: Total Synthesis of Natural Products: The "Chiron" Approach year: 1983 ident: e_1_2_5_155_1 contributor: fullname: Hanessian S – ident: e_1_2_5_19_1 doi: 10.1016/j.jep.2011.07.035 – ident: e_1_2_5_51_1 doi: 10.1021/jo1019877 – ident: e_1_2_5_17_1 doi: 10.1016/0378-8741(95)01342-3 – ident: e_1_2_5_134_1 doi: 10.1002/9783527621071.ch10 – ident: e_1_2_5_15_1 doi: 10.1016/S0040-4039(01)96647-X – ident: e_1_2_5_152_1 doi: 10.1016/S0040-4020(97)00766-7 – ident: e_1_2_5_50_1 doi: 10.2174/1570179413666160624112433 – ident: e_1_2_5_66_1 doi: 10.1080/00397911.2018.1458241 – volume: 49 start-page: 202 year: 2017 ident: e_1_2_5_67_1 article-title: Hydroxyl‐assisted trans‐reduction of 1,3‐enynes: application to the formal synthesis of (+)‐aspicilin publication-title: Synthesis contributor: fullname: Schaubach S – ident: e_1_2_5_65_1 doi: 10.1016/j.tetlet.2006.05.043 – volume: 29 start-page: 998 year: 2018 ident: e_1_2_5_37_1 article-title: Natural products from marine invertebrates and microorganisms in Brazil between 2004 and 2017: still the challenges, more rewards publication-title: J Braz Chem Soc contributor: fullname: Ióca LP – ident: e_1_2_5_128_1 doi: 10.1016/j.tetasy.2011.04.014 – ident: e_1_2_5_26_1 doi: 10.1021/ja01048a062 – ident: e_1_2_5_157_1 doi: 10.1021/cr990374e – ident: e_1_2_5_164_1 doi: 10.1002/anie.198609473 – ident: e_1_2_5_130_1 doi: 10.1016/S0040-4039(00)82216-9 – ident: e_1_2_5_59_1 doi: 10.1016/j.tet.2017.09.041 – ident: e_1_2_5_72_1 doi: 10.1021/jo980942a – ident: e_1_2_5_162_1 doi: 10.1055/s-1997-3185 – ident: e_1_2_5_20_1 doi: 10.1016/S0040-4039(01)95667-9 – ident: e_1_2_5_112_1 doi: 10.1016/j.tet.2007.10.056 – ident: e_1_2_5_167_1 doi: 10.1055/s-1991-26641 – ident: e_1_2_5_44_1 doi: 10.1021/jo0155052 – ident: e_1_2_5_52_1 doi: 10.1016/j.tet.2013.11.046 – ident: e_1_2_5_31_1 doi: 10.1095/biolreprod.112.100438 – ident: e_1_2_5_54_1 doi: 10.1016/S0040-4039(00)61925-1 – ident: e_1_2_5_124_1 doi: 10.3390/molecules171113330 – ident: e_1_2_5_140_1 doi: 10.1021/ja002556s – volume: 1991 start-page: 649 year: 2010 ident: e_1_2_5_169_1 article-title: Carbohydrates as chiral templates: stereoselective Strecker synthesis of d‐α‐amino nitriles and acids using O‐pivaloylated d‐galactosylamine as the auxiliary publication-title: Eur J Org Chem contributor: fullname: Kunz H – ident: e_1_2_5_64_1 doi: 10.1002/jlac.1995199507161 – ident: e_1_2_5_158_1 doi: 10.1021/ja00210a084 – ident: e_1_2_5_88_1 doi: 10.1021/ol100969f – ident: e_1_2_5_98_1 doi: 10.1021/jacs.5b08207 – ident: e_1_2_5_127_1 doi: 10.1021/acs.joc.6b00068 – volume-title: Mannich Bases—Chemistry and Uses year: 1994 ident: e_1_2_5_172_1 contributor: fullname: Tramontini M – ident: e_1_2_5_24_1 doi: 10.1038/nature11411 – ident: e_1_2_5_99_1 doi: 10.1021/jacs.5b10980 – ident: e_1_2_5_90_1 doi: 10.1021/ja0260014 – ident: e_1_2_5_125_1 doi: 10.1039/c3ra41718b – ident: e_1_2_5_146_1 doi: 10.1002/anie.198705571 – ident: e_1_2_5_71_1 doi: 10.1021/ol991214s – ident: e_1_2_5_139_1 doi: 10.1039/a815113y – ident: e_1_2_5_106_1 doi: 10.1021/ja991190k – ident: e_1_2_5_143_1 doi: 10.1039/c4ob00443d – ident: e_1_2_5_38_1 doi: 10.3390/molecules17021177 – ident: e_1_2_5_21_1 doi: 10.1039/c2ob25400j – ident: e_1_2_5_29_1 doi: 10.1016/j.tet.2011.03.064 – ident: e_1_2_5_86_1 doi: 10.1021/ja101913k – ident: e_1_2_5_149_1 doi: 10.1002/anie.199202881 – ident: e_1_2_5_145_1 doi: 10.1002/hlca.19770600417 – ident: e_1_2_5_151_1 doi: 10.1351/pac199567101627 – ident: e_1_2_5_129_1 doi: 10.1246/bcsj.43.2223 – ident: e_1_2_5_16_1 doi: 10.1039/j29700001267 – ident: e_1_2_5_70_1 doi: 10.1016/S0040-4020(00)00337-9 – ident: e_1_2_5_77_1 doi: 10.1016/0040-4039(91)80116-N – ident: e_1_2_5_113_1 doi: 10.1021/acs.joc.6b02838 – volume: 17 start-page: 2685 year: 2011 ident: e_1_2_5_154_1 article-title: More than just sweet–sugar derived stereodifferentiating agents for asymmetric synthesis publication-title: Synthesis contributor: fullname: Lehnert T – ident: e_1_2_5_78_1 doi: 10.1134/S1068162013060095 – ident: e_1_2_5_103_1 doi: 10.1021/ja036414k – ident: e_1_2_5_159_1 doi: 10.1016/S0040-4020(01)86054-3 – ident: e_1_2_5_177_1 doi: 10.1016/0040-4039(94)85031-3 – start-page: 3 volume-title: Asymmetric Synthesis—The Essentials year: 2007 ident: e_1_2_5_2_1 contributor: fullname: Evans DA – ident: e_1_2_5_47_1 doi: 10.1021/ja00258a050 – ident: e_1_2_5_168_1 doi: 10.1002/9783527654543 – ident: e_1_2_5_4_1 doi: 10.1039/C6RA00653A – ident: e_1_2_5_136_1 doi: 10.1021/np034077n – ident: e_1_2_5_40_1 doi: 10.1021/acs.orglett.8b01087 – ident: e_1_2_5_97_1 doi: 10.1039/B617094C – ident: e_1_2_5_101_1 doi: 10.1021/jo0001885 – ident: e_1_2_5_170_1 doi: 10.1016/S0040-4039(00)80504-3 – ident: e_1_2_5_8_1 doi: 10.1021/ja00856a074 – ident: e_1_2_5_68_1 doi: 10.1002/ejoc.201101673 – ident: e_1_2_5_116_1 doi: 10.1021/ja00175a038 – ident: e_1_2_5_57_1 doi: 10.1021/ja954211t – ident: e_1_2_5_118_1 doi: 10.1021/ja00738a045 – ident: e_1_2_5_45_1 doi: 10.1016/S0040-4039(02)02452-8 – ident: e_1_2_5_55_1 doi: 10.1021/ja00165a094 – ident: e_1_2_5_18_1 doi: 10.1002/ardp.19572901002 – ident: e_1_2_5_49_1 doi: 10.1016/S0040-4039(00)71307-4 – ident: e_1_2_5_93_1 doi: 10.1021/jo701849x – ident: e_1_2_5_35_1 doi: 10.1016/S0140-6736(14)62111-5 – volume: 51 start-page: 1 year: 1997 ident: e_1_2_5_84_1 article-title: Asymmetric aldol reactions using boron enolates publication-title: Org React contributor: fullname: Cowden CJ – start-page: 273 volume-title: Second Supplement to the Second Edition of Rodd's Chemistry of Carbon Compounds, Vol. 1E/F/G year: 1993 ident: e_1_2_5_150_1 contributor: fullname: Hale KJ – ident: e_1_2_5_119_1 doi: 10.1021/ja00064a011 – ident: e_1_2_5_13_1 doi: 10.1016/S0040-4039(01)88663-9 – start-page: 355 volume-title: Comprehensive Organic Synthesis year: 2007 ident: e_1_2_5_173_1 contributor: fullname: Trost B – ident: e_1_2_5_92_1 doi: 10.1016/j.tet.2009.08.042 – ident: e_1_2_5_62_1 doi: 10.1016/S0040-4039(97)00482-6 – start-page: 375 volume-title: Drug Stereochemistry: Analytical Methods and Pharmacology year: 1993 ident: e_1_2_5_3_1 contributor: fullname: Fakhreddin J – ident: e_1_2_5_165_1 doi: 10.1016/j.tet.2012.03.115 – ident: e_1_2_5_141_1 doi: 10.1016/j.tetlet.2008.10.074 – ident: e_1_2_5_60_1 doi: 10.1055/s-0032-1316865 – ident: e_1_2_5_148_1 doi: 10.1016/S0040-4020(01)86544-3 – ident: e_1_2_5_39_1 doi: 10.1080/09546630410017275 – ident: e_1_2_5_131_1 doi: 10.1016/j.tetlet.2012.04.042 |
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SubjectTerms | Amino acids Asymmetric synthesis Asymmetry Bioactive compounds Biological activity biologically active compounds Carbohydrates chiral auxiliaries Corey's chiral auxiliary Evans' oxazolidinones Modularity Synthesis Terpenes |
Title | Use of chiral auxiliaries in the asymmetric synthesis of biologically active compounds: A review |
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