Transition Metal‐Catalyzed Dicarbofunctionalization of Unactivated Olefins
Transition metal (TM)‐catalyzed difunctionalization of unactivated olefins with two carbon‐based entities is a powerful method to construct complex molecular architectures rapidly from simple and readily available feedstock chemicals. While dicarbofunctionalization of unactivated olefins has a long...
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| Published in | Chemical record Vol. 18; no. 9; pp. 1314 - 1340 |
|---|---|
| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Wiley Subscription Services, Inc
01.09.2018
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| Subjects | |
| Online Access | Get full text |
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| Abstract | Transition metal (TM)‐catalyzed difunctionalization of unactivated olefins with two carbon‐based entities is a powerful method to construct complex molecular architectures rapidly from simple and readily available feedstock chemicals. While dicarbofunctionalization of unactivated olefins has a long history typically with the use of either carbon monoxide to intercept C(sp3)‐[M] (alkyl‐TM) species or substrates lacking in β‐hydrogen (β‐Hs), development of this class of reaction still remains seriously limited due to complications of β‐H elimination arising from the in situ‐generated C(sp3)‐[M] intermediates. Over the years, different approaches have been harnessed to suppress β‐H elimination, which have led to the development of various types of olefin dicarbofunctionalization reactions even in substrates that generate C(sp3)‐[M] intermediates bearing β‐Hs with a wide range of electrophiles and nucleophiles. In this review, these developments will be discussed both through the lens of historical perspectives as well as the strategies scrutinized over the years to address the issue of β‐H elimination. However, this review article by no means is designed to be exhaustive in the field, and is merely presented to provide the readers an overview of the key reaction developments.
Various transition metal‐catalyzed dicarbofunctionalization reactions of olefins are described. These reactions are conducted with transition metals such as Ti, Cr, Mn, Fe, Co, Ni, Cu, Rh and Pd, and are performed both intra‐ and intermolecularly in two‐, three‐ and multi‐component manners to contruct complex carbon skeletons from simple and readily available feedstock chemicals. |
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| AbstractList | Transition metal (TM)‐catalyzed difunctionalization of unactivated olefins with two carbon‐based entities is a powerful method to construct complex molecular architectures rapidly from simple and readily available feedstock chemicals. While dicarbofunctionalization of unactivated olefins has a long history typically with the use of either carbon monoxide to intercept C(sp3)‐[M] (alkyl‐TM) species or substrates lacking in β‐hydrogen (β‐Hs), development of this class of reaction still remains seriously limited due to complications of β‐H elimination arising from the in situ‐generated C(sp3)‐[M] intermediates. Over the years, different approaches have been harnessed to suppress β‐H elimination, which have led to the development of various types of olefin dicarbofunctionalization reactions even in substrates that generate C(sp3)‐[M] intermediates bearing β‐Hs with a wide range of electrophiles and nucleophiles. In this review, these developments will be discussed both through the lens of historical perspectives as well as the strategies scrutinized over the years to address the issue of β‐H elimination. However, this review article by no means is designed to be exhaustive in the field, and is merely presented to provide the readers an overview of the key reaction developments. Transition metal (TM)‐catalyzed difunctionalization of unactivated olefins with two carbon‐based entities is a powerful method to construct complex molecular architectures rapidly from simple and readily available feedstock chemicals. While dicarbofunctionalization of unactivated olefins has a long history typically with the use of either carbon monoxide to intercept C(sp 3 )‐[M] (alkyl‐TM) species or substrates lacking in β‐hydrogen (β‐Hs), development of this class of reaction still remains seriously limited due to complications of β‐H elimination arising from the in situ‐generated C(sp 3 )‐[M] intermediates. Over the years, different approaches have been harnessed to suppress β‐H elimination, which have led to the development of various types of olefin dicarbofunctionalization reactions even in substrates that generate C(sp 3 )‐[M] intermediates bearing β‐Hs with a wide range of electrophiles and nucleophiles. In this review, these developments will be discussed both through the lens of historical perspectives as well as the strategies scrutinized over the years to address the issue of β‐H elimination. However, this review article by no means is designed to be exhaustive in the field, and is merely presented to provide the readers an overview of the key reaction developments. Transition metal (TM)-catalyzed difunctionalization of unactivated olefins with two carbon-based entities is a powerful method to construct complex molecular architectures rapidly from simple and readily available feedstock chemicals. While dicarbofunctionalization of unactivated olefins has a long history typically with the use of either carbon monoxide to intercept C(sp3 )-[M] (alkyl-TM) species or substrates lacking in β-hydrogen (β-Hs), development of this class of reaction still remains seriously limited due to complications of β-H elimination arising from the in situ-generated C(sp3 )-[M] intermediates. Over the years, different approaches have been harnessed to suppress β-H elimination, which have led to the development of various types of olefin dicarbofunctionalization reactions even in substrates that generate C(sp3 )-[M] intermediates bearing β-Hs with a wide range of electrophiles and nucleophiles. In this review, these developments will be discussed both through the lens of historical perspectives as well as the strategies scrutinized over the years to address the issue of β-H elimination. However, this review article by no means is designed to be exhaustive in the field, and is merely presented to provide the readers an overview of the key reaction developments.Transition metal (TM)-catalyzed difunctionalization of unactivated olefins with two carbon-based entities is a powerful method to construct complex molecular architectures rapidly from simple and readily available feedstock chemicals. While dicarbofunctionalization of unactivated olefins has a long history typically with the use of either carbon monoxide to intercept C(sp3 )-[M] (alkyl-TM) species or substrates lacking in β-hydrogen (β-Hs), development of this class of reaction still remains seriously limited due to complications of β-H elimination arising from the in situ-generated C(sp3 )-[M] intermediates. Over the years, different approaches have been harnessed to suppress β-H elimination, which have led to the development of various types of olefin dicarbofunctionalization reactions even in substrates that generate C(sp3 )-[M] intermediates bearing β-Hs with a wide range of electrophiles and nucleophiles. In this review, these developments will be discussed both through the lens of historical perspectives as well as the strategies scrutinized over the years to address the issue of β-H elimination. However, this review article by no means is designed to be exhaustive in the field, and is merely presented to provide the readers an overview of the key reaction developments. Transition metal (TM)‐catalyzed difunctionalization of unactivated olefins with two carbon‐based entities is a powerful method to construct complex molecular architectures rapidly from simple and readily available feedstock chemicals. While dicarbofunctionalization of unactivated olefins has a long history typically with the use of either carbon monoxide to intercept C(sp3)‐[M] (alkyl‐TM) species or substrates lacking in β‐hydrogen (β‐Hs), development of this class of reaction still remains seriously limited due to complications of β‐H elimination arising from the in situ‐generated C(sp3)‐[M] intermediates. Over the years, different approaches have been harnessed to suppress β‐H elimination, which have led to the development of various types of olefin dicarbofunctionalization reactions even in substrates that generate C(sp3)‐[M] intermediates bearing β‐Hs with a wide range of electrophiles and nucleophiles. In this review, these developments will be discussed both through the lens of historical perspectives as well as the strategies scrutinized over the years to address the issue of β‐H elimination. However, this review article by no means is designed to be exhaustive in the field, and is merely presented to provide the readers an overview of the key reaction developments. Various transition metal‐catalyzed dicarbofunctionalization reactions of olefins are described. These reactions are conducted with transition metals such as Ti, Cr, Mn, Fe, Co, Ni, Cu, Rh and Pd, and are performed both intra‐ and intermolecularly in two‐, three‐ and multi‐component manners to contruct complex carbon skeletons from simple and readily available feedstock chemicals. Transition metal (TM)-catalyzed difunctionalization of unactivated olefins with two carbon-based entities is a powerful method to construct complex molecular architectures rapidly from simple and readily available feedstock chemicals. While dicarbofunctionalization of unactivated olefins has a long history typically with the use of either carbon monoxide to intercept C(sp )-[M] (alkyl-TM) species or substrates lacking in β-hydrogen (β-Hs), development of this class of reaction still remains seriously limited due to complications of β-H elimination arising from the in situ-generated C(sp )-[M] intermediates. Over the years, different approaches have been harnessed to suppress β-H elimination, which have led to the development of various types of olefin dicarbofunctionalization reactions even in substrates that generate C(sp )-[M] intermediates bearing β-Hs with a wide range of electrophiles and nucleophiles. In this review, these developments will be discussed both through the lens of historical perspectives as well as the strategies scrutinized over the years to address the issue of β-H elimination. However, this review article by no means is designed to be exhaustive in the field, and is merely presented to provide the readers an overview of the key reaction developments. |
| Author | KC, Shekhar Dhungana, Roshan K. Giri, Ramesh Basnet, Prakash |
| Author_xml | – sequence: 1 givenname: Roshan K. surname: Dhungana fullname: Dhungana, Roshan K. organization: The University of New Mexico – sequence: 2 givenname: Shekhar surname: KC fullname: KC, Shekhar organization: The University of New Mexico – sequence: 3 givenname: Prakash surname: Basnet fullname: Basnet, Prakash organization: The University of New Mexico – sequence: 4 givenname: Ramesh surname: Giri fullname: Giri, Ramesh email: rgiri@unm.edu organization: The University of New Mexico |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29517841$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1021/jacs.6b13299 10.1246/cl.1987.193 10.1002/(SICI)1521-3773(19980202)37:1/2<152::AID-ANIE152>3.0.CO;2-8 10.1021/jacs.7b12160 10.1016/0040-4020(89)80008-0 10.1016/S0040-4020(97)00754-0 10.1021/ja00312a095 10.1039/b813246a 10.1016/S0040-4039(00)93407-5 10.1021/ja054754v 10.1021/acs.orglett.6b00447 10.1021/jacs.7b10529 10.1055/s-2006-951508 10.1039/b306797c 10.1016/j.tetlet.2012.02.096 10.1055/s-2003-42082 10.1021/ol0356643 10.1021/ja210307s 10.1021/ja00437a018 10.1021/jo00977a038 10.1021/ja046810i 10.1016/S0040-4020(01)80763-8 10.1021/ol200536h 10.1021/ja304344h 10.1002/anie.198701531 10.1016/0040-4039(95)01676-9 10.1021/jo1002032 10.1021/ja309978c 10.1002/anie.200900218 10.1021/jo202221c 10.1021/ja8066308 10.1021/cr00032a009 10.1021/cr100327p 10.1021/ja412881j 10.1021/ja8084065 10.1038/nrd2060 10.1016/S0010-8545(96)90182-4 10.1016/S0040-4020(00)01030-9 10.1021/jo025665t 10.1021/ja504458j 10.1021/acs.orglett.6b00517 10.1055/s-0036-1588804 10.1021/ja3110544 10.1002/anie.201607976 10.1016/S0040-4020(00)00661-X 10.1002/anie.200500195 10.1021/jacs.6b10468 10.1002/anie.201511624 10.1002/9783527612222 10.1016/S0040-4020(01)90073-0 10.1021/jo00239a054 10.1021/ol049702 10.1039/C4SC03074E 10.1021/jo960677y 10.1055/s-1998-6086 10.1021/ja109686v 10.1021/ja00191a066 10.1002/anie.201311009 10.1016/S0040-4039(00)92673-X 10.1021/ol4023358 10.1016/S0040-4039(01)01811-1 10.1021/ja0100423 10.1021/acs.orglett.5b00775 10.1021/ja909555d 10.1021/acs.orglett.6b02665 10.1021/acs.organomet.6b00532 10.1021/ja1034123 10.1021/jacs.5b10176 10.1021/ol303003g 10.1002/anie.200702528 10.1021/ja045047p 10.1016/S0040-4039(00)74293-6 10.1021/cr0505268 10.1021/ol4009848 10.1039/b918358b 10.1021/jo0255779 10.1126/science.aaf6123 10.1002/anie.200500368 10.1016/j.tet.2015.03.012 10.1021/cr9903048 10.1021/jacs.6b09170 10.1021/ja00317a059 10.1002/tcr.10026 10.1021/ja201358b 10.1016/S0040-4039(00)80814-X 10.1246/bcsj.66.3522 10.1016/S0040-4039(00)96556-0 10.1021/ja054549f 10.1002/anie.201600379 10.1021/ja0762240 10.1055/s-0032-1316555 10.1021/ja0460920 10.1021/jm0512903 10.1002/anie.201210250 10.1039/C7SC03149A 10.1021/ol1009575 10.1021/ol502279u 10.1021/ja00796a056 10.1002/anie.201107017 10.1021/jacs.5b07203 10.1021/ol0056426 10.1002/adsc.200404041 10.1016/0022-328X(84)80586-0 10.1002/anie.201402462 10.1039/c39950000295 10.1016/S0040-4039(97)00195-0 10.1021/acs.orglett.6b02154 10.1021/jacs.7b03195 10.1002/chem.201300882 10.1021/jacs.5b08734 10.1039/b820636h 10.1080/00397918708063944 10.1002/anie.201108446 10.1021/ol901799p 10.1021/jacs.7b06917 10.1021/jo960617s 10.1016/S0040-4039(00)73183-2 10.1021/ja500706v 10.1002/open.201100010 10.1002/(SICI)1521-3773(19990517)38:10<1452::AID-ANIE1452>3.0.CO;2-P 10.1016/j.jfluchem.2014.04.004 10.1021/ja00105a096 10.1021/cr00026a008 10.1016/B978-0-08-052349-1.00110-4 10.1002/anie.201303724 10.1021/jo016212b 10.1039/C3CC47780K 10.1021/jacs.5b04691 10.1002/anie.201500636 10.1021/jacs.6b02158 10.1016/S0040-4020(01)80760-2 10.1039/C7SC01204G 10.1021/acs.orglett.5b01722 10.1021/ja00423a028 10.1021/jacs.7b06567 10.1021/om700311x 10.1021/jacs.7b06191 10.1002/ejoc.201403511 10.1002/anie.201101857 10.1021/cr800420x 10.1021/ja052099l 10.1016/S0040-4039(00)85642-7 10.1021/ja982732l 10.1021/ja3034075 10.1021/cr900184e 10.1002/anie.201404802 10.1021/acs.orglett.7b01036 10.1021/ja0430346 10.1016/S0040-4020(00)00659-1 10.1021/ja00068a092 10.1002/anie.201606458 10.1016/0040-4039(95)01696-F 10.1021/jo401831t 10.1016/S0040-4020(01)88469-6 10.1002/chem.201200190 10.1021/ja9533196 10.1021/jo402705w 10.1021/om00125a008 10.1016/j.tet.2004.03.023 10.1021/ol403263c 10.1002/ejoc.200300543 10.1002/anie.201202771 10.1021/ja00763a028 10.1016/S0040-4039(96)02442-2 10.1002/anie.201002739 10.1515/pac-2014-5041 10.1002/anie.200903178 10.1039/b816707a 10.1021/ja017315e 10.1021/jacs.7b01922 10.1016/S0040-4020(01)81100-5 10.1021/ar9000058 10.1021/jm9806998 10.1016/j.tet.2015.06.030 10.1021/ol9900663 10.1016/0040-4039(91)80445-C 10.2533/chimia.2015.187 10.1002/chem.19960021006 10.1002/anie.198707711 10.1039/C7SC04351A 10.1021/cr020027w 10.1021/ja2091883 10.1021/ol801168j 10.1021/jacs.7b06340 10.1021/acs.chemrev.6b00833 10.1039/C6CC10075A 10.1021/jo1018188 10.1021/jo0625958 10.1016/S0040-4039(00)98060-2 10.1021/ja9533205 10.1021/acs.orglett.7b00794 10.1021/ja509056j |
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| References | 2010; 12 1973; 95 1989; 45 2015; 71 1995; 36 1989; 111 2004; 6 1999; 42 2012; 18 2007; 72 2014; 136 2011; 111 2016; 35 2001; 42 2009; 11 2018; 9 1993; 34 1984; 275 2012; 134 1990; 46 2015; 137 1997; 53 2013; 52 2014; 16 2010; 110 1996; 61 2006; 2006 1992; 48 2001; 57 2012; 23 1998; 1998 1990; 31 2003; 2003 1984; 106 2015; 54 1998 2002; 2 2011; 76 1995 1991 2016; 18 1992; 33 2011; 133 2017; 139 2017; 53 2015; 69 2010; 49 2006; 45 1988; 29 2013; 78 2002; 67 2006; 49 2002; 124 1999; 38 2005; 127 2015; 2015 1997; 38 2000; 100 2003; 103 1994; 94 2006; 106 1993; 115 2003; 20 1996; 118 2017; 8 2004; 126 2009; 42 2004; 60 2017; 49 1993; 66 2011; 13 2000; 2 2008; 6 2009; 48 2012; 53 2017; 117 2012; 51 1982; 23 2013; 19 2013; 15 2000; 56 1972; 94 2016; 352 2003; 5 1994; 35 2014; 50 1996; 2 1998; 120 2014; 167 2007; 26 2014; 53 2010; 75 2001; 123 2007; 129 2015; 6 2015; 17 1994; 116 2004; 346 2018; 140 1985; 4 1991; 32 2009 2006; 5 2008; 10 1985; 107 2009; 131 1988; 53 1999; 1 2012; 77 2005; 44 1987; 17 2016; 55 1987; 16 2014; 86 1976; 98 1998; 37 2012; 1 2011; 50 2010; 132 2018 2014; 79 2013; 135 2016 2017; 19 1996; 155 2016; 138 1994; 50 2009; 38 1987; 28 2007; 46 1987; 26 1972; 37 e_1_2_6_114_1 e_1_2_6_137_1 e_1_2_6_53_1 e_1_2_6_76_1 e_1_2_6_30_2 e_1_2_6_91_2 e_1_2_6_198_1 e_1_2_6_152_2 e_1_2_6_175_2 e_1_2_6_38_2 e_1_2_6_15_1 e_1_2_6_99_1 e_1_2_6_212_2 e_1_2_6_125_2 e_1_2_6_64_1 e_1_2_6_148_1 e_1_2_6_41_1 e_1_2_6_140_2 e_1_2_6_186_2 e_1_2_6_163_1 e_1_2_6_102_1 e_1_2_6_200_1 e_1_2_6_223_1 e_1_2_6_5_1 e_1_2_6_208_1 e_1_2_6_49_2 e_1_2_6_87_2 e_1_2_6_26_2 e_1_2_6_136_2 e_1_2_6_159_1 e_1_2_6_31_2 e_1_2_6_92_2 e_1_2_6_151_2 Iwasaki T. (e_1_2_6_68_2) 2018 e_1_2_6_174_1 e_1_2_6_113_1 e_1_2_6_197_1 e_1_2_6_211_1 e_1_2_6_219_1 e_1_2_6_16_2 e_1_2_6_39_2 e_1_2_6_54_2 e_1_2_6_77_1 e_1_2_6_147_1 e_1_2_6_42_2 e_1_2_6_65_1 e_1_2_6_80_2 e_1_2_6_109_1 e_1_2_6_162_1 e_1_2_6_101_1 e_1_2_6_124_1 e_1_2_6_185_2 e_1_2_6_222_1 e_1_2_6_6_2 e_1_2_6_207_1 e_1_2_6_88_2 e_1_2_6_27_1 e_1_2_6_74_1 e_1_2_6_97_1 e_1_2_6_51_2 e_1_2_6_135_2 e_1_2_6_158_2 e_1_2_6_150_1 e_1_2_6_173_1 e_1_2_6_112_1 e_1_2_6_196_1 e_1_2_6_210_1 e_1_2_6_59_1 e_1_2_6_13_2 e_1_2_6_218_1 e_1_2_6_36_2 e_1_2_6_85_1 e_1_2_6_62_2 e_1_2_6_169_2 e_1_2_6_108_1 e_1_2_6_161_1 e_1_2_6_100_1 e_1_2_6_146_1 e_1_2_6_184_1 e_1_2_6_123_1 e_1_2_6_221_1 e_1_2_6_3_2 e_1_2_6_24_2 e_1_2_6_206_1 e_1_2_6_47_1 e_1_2_6_52_1 e_1_2_6_98_1 e_1_2_6_157_2 e_1_2_6_75_1 e_1_2_6_119_2 e_1_2_6_90_1 e_1_2_6_172_2 e_1_2_6_111_1 e_1_2_6_195_1 e_1_2_6_134_1 e_1_2_6_160_1 e_1_2_6_217_2 e_1_2_6_14_2 e_1_2_6_37_2 e_1_2_6_63_1 e_1_2_6_86_2 e_1_2_6_168_2 e_1_2_6_107_1 e_1_2_6_40_2 e_1_2_6_122_1 e_1_2_6_145_1 e_1_2_6_183_1 e_1_2_6_220_1 e_1_2_6_4_2 e_1_2_6_48_1 e_1_2_6_205_2 e_1_2_6_25_2 e_1_2_6_95_2 e_1_2_6_118_2 e_1_2_6_72_1 e_1_2_6_171_2 e_1_2_6_110_1 e_1_2_6_179_1 e_1_2_6_194_1 e_1_2_6_156_2 e_1_2_6_133_2 e_1_2_6_19_2 e_1_2_6_182_1 e_1_2_6_34_2 e_1_2_6_11_2 e_1_2_6_216_2 e_1_2_6_57_1 e_1_2_6_83_2 e_1_2_6_106_1 e_1_2_6_129_2 e_1_2_6_60_1 e_1_2_6_144_2 e_1_2_6_121_1 e_1_2_6_167_1 e_1_2_6_9_2 e_1_2_6_170_1 e_1_2_6_1_1 e_1_2_6_22_2 e_1_2_6_45_1 e_1_2_6_204_2 e_1_2_6_50_2 e_1_2_6_73_1 e_1_2_6_96_1 e_1_2_6_117_2 e_1_2_6_132_2 e_1_2_6_155_2 e_1_2_6_193_2 e_1_2_6_178_1 e_1_2_6_181_1 e_1_2_6_12_2 e_1_2_6_35_2 e_1_2_6_215_1 e_1_2_6_58_1 e_1_2_6_61_2 e_1_2_6_84_2 e_1_2_6_105_1 e_1_2_6_128_1 e_1_2_6_120_1 e_1_2_6_189_1 e_1_2_6_166_2 e_1_2_6_143_2 e_1_2_6_192_2 e_1_2_6_23_2 e_1_2_6_2_1 e_1_2_6_203_2 e_1_2_6_226_1 e_1_2_6_46_1 e_1_2_6_69_1 e_1_2_6_116_1 e_1_2_6_93_2 e_1_2_6_139_2 e_1_2_6_70_2 e_1_2_6_131_1 e_1_2_6_154_1 e_1_2_6_177_1 e_1_2_6_180_1 Haas D. (e_1_2_6_10_2) 2016 e_1_2_6_32_2 e_1_2_6_78_1 e_1_2_6_17_2 e_1_2_6_55_2 e_1_2_6_214_1 e_1_2_6_104_1 e_1_2_6_127_1 e_1_2_6_20_2 e_1_2_6_81_2 e_1_2_6_142_1 e_1_2_6_188_2 e_1_2_6_165_2 e_1_2_6_7_2 e_1_2_6_191_1 e_1_2_6_28_2 e_1_2_6_43_2 e_1_2_6_66_1 e_1_2_6_89_1 e_1_2_6_202_1 e_1_2_6_225_1 e_1_2_6_115_1 e_1_2_6_94_2 e_1_2_6_138_1 e_1_2_6_71_2 e_1_2_6_153_1 e_1_2_6_199_1 e_1_2_6_130_2 e_1_2_6_176_2 e_1_2_6_18_2 e_1_2_6_33_2 e_1_2_6_56_1 e_1_2_6_79_2 e_1_2_6_213_2 e_1_2_6_103_1 e_1_2_6_149_1 e_1_2_6_126_2 e_1_2_6_82_2 e_1_2_6_141_1 e_1_2_6_164_1 e_1_2_6_187_2 e_1_2_6_8_2 e_1_2_6_190_1 e_1_2_6_201_1 e_1_2_6_29_2 e_1_2_6_209_1 e_1_2_6_21_2 e_1_2_6_44_2 e_1_2_6_67_2 e_1_2_6_224_1 |
| References_xml | – volume: 6 start-page: 4083 year: 2008 end-page: 4088 publication-title: Org. Biomol. Chem. – volume: 352 start-page: 801 year: 2016 end-page: 805 publication-title: Science – volume: 55 start-page: 14389 year: 2016 end-page: 14393 publication-title: Angew. Chem. Int. Ed. – volume: 20 start-page: 558 year: 2003 end-page: 564 publication-title: Nat. Prod. Rep. – start-page: 7587 year: 2009 end-page: 7589 publication-title: Chem. Commun. – volume: 1 start-page: 49 year: 2012 end-page: 56 publication-title: ChemistryOpen – volume: 5 start-page: 493 year: 2006 publication-title: Nat. Rev. Drug Discov. – volume: 131 start-page: 2052 year: 2009 end-page: 2053 publication-title: J. Am. Chem. Soc. – volume: 55 start-page: 3187 year: 2016 end-page: 3191 publication-title: Angew. Chem. Int. Ed. – volume: 129 start-page: 12948 year: 2007 end-page: 12949 publication-title: J. Am. Chem. Soc. – volume: 5 start-page: 3959 year: 2003 end-page: 3961 publication-title: Org. Lett. – volume: 138 start-page: 15122 year: 2016 end-page: 15125 publication-title: J. Am. Chem. Soc. – volume: 134 start-page: 11372 year: 2012 end-page: 11375 publication-title: J. Am. Chem. Soc. – volume: 53 start-page: 6383 year: 2014 end-page: 6387 publication-title: Angew. Chem. Int. Ed. – volume: 4 start-page: 1006 year: 1985 end-page: 1014 publication-title: Organometallics – volume: 51 start-page: 5062 year: 2012 end-page: 5085 publication-title: Angew. Chem. Int. Ed. – volume: 137 start-page: 11246 year: 2015 end-page: 11249 publication-title: J. Am. Chem. Soc. – volume: 38 start-page: 1452 year: 1999 end-page: 1454 publication-title: Angew. Chem. Int. Ed. – volume: 111 start-page: 1417 year: 2011 end-page: 1492 publication-title: Chem. Rev. – volume: 11 start-page: 4560 year: 2009 end-page: 4563 publication-title: Org. Lett. – volume: 132 start-page: 8885 year: 2010 end-page: 8887 publication-title: J. Am. Chem. Soc. – volume: 18 start-page: 5170 year: 2016 end-page: 5173 publication-title: Org. Lett. – volume: 56 start-page: 7553 year: 2000 end-page: 7560 publication-title: Tetrahedron – volume: 12 start-page: 2848 year: 2010 end-page: 2851 publication-title: Org. Lett. – volume: 46 start-page: 8790 year: 2007 end-page: 8795 publication-title: Angew. Chem. Int. Ed. – volume: 52 start-page: 9284 year: 2013 end-page: 9288 publication-title: Angew. Chem. Int. Ed. – volume: 98 start-page: 6521 year: 1976 end-page: 6528 publication-title: J. Am. Chem. Soc. – volume: 61 start-page: 5743 year: 1996 end-page: 5753 publication-title: J. Org. Chem. – volume: 131 start-page: 412 year: 2009 end-page: 413 publication-title: J. Am. Chem. Soc. – volume: 140 start-page: 58 year: 2018 end-page: 61 publication-title: J. Am. Chem. Soc. – volume: 36 start-page: 8019 year: 1995 end-page: 8022 publication-title: Tetrahedron Lett. – volume: 118 start-page: 5904 year: 1996 end-page: 5918 publication-title: J. Am. Chem. Soc. – volume: 126 start-page: 16820 year: 2004 end-page: 16833 publication-title: J. Am. Chem. Soc. – volume: 36 start-page: 8137 year: 1995 end-page: 8140 publication-title: Tetrahedron Lett. – volume: 103 start-page: 2921 year: 2003 end-page: 2944 publication-title: Chem. Rev. – volume: 15 start-page: 5008 year: 2013 end-page: 5011 publication-title: Org. Lett. – volume: 32 start-page: 1641 year: 1991 end-page: 1644 publication-title: Tetrahedron Lett. – volume: 110 start-page: 2366 year: 2010 end-page: 2447 publication-title: Chem. Rev. – volume: 35 start-page: 1871 year: 1994 end-page: 1874 publication-title: Tetrahedron Lett. – volume: 38 start-page: 827 year: 1997 end-page: 830 publication-title: Tetrahedron Lett. – volume: 37 start-page: 152 year: 1998 end-page: 155 publication-title: Angew. Chem. Int. Ed. – volume: 71 start-page: 5959 year: 2015 end-page: 5964 publication-title: Tetrahedron – volume: 35 start-page: 3170 year: 2016 end-page: 3181 publication-title: Organometallics – volume: 42 start-page: 3251 year: 1999 end-page: 3264 publication-title: J. Med. Chem. – volume: 29 start-page: 5565 year: 1988 end-page: 5568 publication-title: Tetrahedron Lett. – volume: 127 start-page: 16468 year: 2005 end-page: 16476 publication-title: J. Am. Chem. Soc. – volume: 28 start-page: 4533 year: 1987 end-page: 4536 publication-title: Tetrahedron Lett. – volume: 2015 start-page: 1781 year: 2015 end-page: 1789 publication-title: Eur. J. Org. Chem. – volume: 45 start-page: 961 year: 1989 end-page: 967 publication-title: Tetrahedron – volume: 31 start-page: 5319 year: 1990 end-page: 5322 publication-title: Tetrahedron Lett. – volume: 78 start-page: 11087 year: 2013 end-page: 11091 publication-title: J. Org. Chem. – volume: 46 start-page: 7763 year: 1990 end-page: 7774 publication-title: Tetrahedron – volume: 16 start-page: 4666 year: 2014 end-page: 4669 publication-title: Org. Lett. – volume: 10 start-page: 3303 year: 2008 end-page: 3306 publication-title: Org. Lett. – volume: 136 start-page: 10202 year: 2014 end-page: 10205 publication-title: J. Am. Chem. Soc. – volume: 134 start-page: 715 year: 2012 end-page: 722 publication-title: J. Am. Chem. Soc. – volume: 139 start-page: 10228 year: 2017 end-page: 10231 publication-title: J. Am. Chem. Soc. – volume: 66 start-page: 3522 year: 1993 end-page: 3524 publication-title: Bull. Chem. Soc. Jpn. – volume: 2 start-page: 249 year: 2002 end-page: 258 publication-title: Chem. Rec. – start-page: 1571 year: 2009 end-page: 1573 publication-title: Chem. Commun. – volume: 6 start-page: 1573 year: 2004 end-page: 1575 publication-title: Org. Lett. – volume: 17 start-page: 3742 year: 2015 end-page: 3745 publication-title: Org. Lett. – volume: 18 start-page: 4148 year: 2016 end-page: 4150 publication-title: Org. Lett. – volume: 56 start-page: 7525 year: 2000 end-page: 7539 publication-title: Tetrahedron – volume: 133 start-page: 2031 year: 2011 end-page: 2033 publication-title: J. Am. Chem. Soc. – volume: 136 start-page: 3788 year: 2014 end-page: 3791 publication-title: J. Am. Chem. Soc. – volume: 127 start-page: 13154 year: 2005 end-page: 13155 publication-title: J. Am. Chem. Soc. – volume: 72 start-page: 3145 year: 2007 end-page: 3148 publication-title: J. Org. Chem. – volume: 49 start-page: 3033 year: 2006 end-page: 3044 publication-title: J. Med. Chem. – start-page: 6 year: 2016 end-page: 1552 publication-title: ACS Catal. – volume: 55 start-page: 5044 year: 2016 end-page: 5048 publication-title: Angew. Chem. Int. Ed. – volume: 53 start-page: 913 year: 1988 end-page: 915 publication-title: J. Org. Chem. – volume: 118 start-page: 5919 year: 1996 end-page: 5931 publication-title: J. Am. Chem. Soc. – volume: 18 start-page: 6039 year: 2012 end-page: 6048 publication-title: Chem. Eur. J. – volume: 134 start-page: 20005 year: 2012 end-page: 20008 publication-title: J. Am. Chem. Soc. – volume: 132 start-page: 1474 year: 2010 end-page: 1475 publication-title: J. Am. Chem. Soc. – volume: 51 start-page: 7567 year: 2012 end-page: 7571 publication-title: Angew. Chem. Int. Ed. – volume: 13 start-page: 2114 year: 2011 end-page: 2117 publication-title: Org. Lett. – volume: 34 start-page: 3163 year: 1993 end-page: 3164 publication-title: Tetrahedron Lett. – volume: 44 start-page: 4442 year: 2005 end-page: 4489 publication-title: Angew. Chem. Int. Ed. – volume: 111 start-page: 3454 year: 1989 end-page: 3456 publication-title: J. Am. Chem. Soc. – volume: 117 start-page: 11680 year: 2017 end-page: 11752 publication-title: Chem. Rev. – volume: 55 start-page: 12270 year: 2016 end-page: 12274 publication-title: Angew. Chem. Int. Ed. – volume: 26 start-page: 771 year: 1987 end-page: 773 publication-title: Angew. Chem. Int. Ed. – volume: 134 start-page: 12149 year: 2012 end-page: 12156 publication-title: J. Am. Chem. Soc. – volume: 86 start-page: 395 year: 2014 publication-title: Pure Appl. Chem. – volume: 6 start-page: 1355 year: 2015 end-page: 1361 publication-title: Chem. Sci. – volume: 106 start-page: 1496 year: 1984 end-page: 1498 publication-title: J. Am. Chem. Soc. – volume: 275 start-page: 129 year: 1984 end-page: 138 publication-title: J. Organomet. Chem. – volume: 67 start-page: 7155 year: 2002 end-page: 7157 publication-title: J. Org. Chem. – volume: 137 start-page: 14578 year: 2015 end-page: 14581 publication-title: J. Am. Chem. Soc. – volume: 138 start-page: 15547 year: 2016 end-page: 15550 publication-title: J. Am. Chem. Soc. – volume: 50 start-page: 6626 year: 2011 end-page: 6629 publication-title: Angew. Chem. Int. Ed. – volume: 15 start-page: 2502 year: 2013 end-page: 2505 publication-title: Org. Lett. – volume: 42 start-page: 8677 year: 2001 end-page: 8680 publication-title: Tetrahedron Lett. – volume: 77 start-page: 999 year: 2012 end-page: 1009 publication-title: J. Org. Chem. – volume: 23 start-page: 2749 year: 2012 end-page: 2752 publication-title: Synlett – volume: 18 start-page: 1784 year: 2016 end-page: 1787 publication-title: Org. Lett. – volume: 2003 start-page: 4346 year: 2003 end-page: 4348 publication-title: Eur. J. Org. Chem. – volume: 94 start-page: 2712 year: 1972 end-page: 2716 publication-title: J. Am. Chem. Soc. – volume: 19 start-page: 2154 year: 2017 end-page: 2157 publication-title: Org. Lett. – volume: 127 start-page: 10323 year: 2005 end-page: 10333 publication-title: J. Am. Chem. Soc. – volume: 155 start-page: 209 year: 1996 end-page: 243 publication-title: Coord. Chem. Rev. – volume: 1 start-page: 165 year: 1999 end-page: 168 publication-title: Org. Lett. – volume: 76 start-page: 2433 year: 2011 end-page: 2438 publication-title: J. Org. Chem. – volume: 19 start-page: 2702 year: 2017 end-page: 2705 publication-title: Org. Lett. – volume: 9 start-page: 600 year: 2018 end-page: 607 publication-title: Chem. Sci. – volume: 95 start-page: 5062 year: 1973 end-page: 5064 publication-title: J. Am. Chem. Soc. – volume: 100 start-page: 3009 year: 2000 end-page: 3066 publication-title: Chem. Rev. – volume: 167 start-page: 55 year: 2014 end-page: 60 publication-title: J. Fluorine Chem. – volume: 94 start-page: 2483 year: 1994 end-page: 2547 publication-title: Chem. Rev. – volume: 53 start-page: 11803 year: 1997 end-page: 11826 publication-title: Tetrahedron – year: 1998 – volume: 16 start-page: 193 year: 1987 end-page: 194 publication-title: Chem. Lett. – volume: 57 start-page: 607 year: 2001 end-page: 615 publication-title: Tetrahedron – volume: 48 start-page: 7224 year: 2009 end-page: 7226 publication-title: Angew. Chem. Int. Ed. – volume: 18 start-page: 1792 year: 2016 end-page: 1795 publication-title: Org. Lett. – volume: 49 start-page: 5519 year: 2010 end-page: 5522 publication-title: Angew. Chem. Int. Ed. – volume: 16 start-page: 270 year: 2014 end-page: 273 publication-title: Org. Lett. – volume: 137 start-page: 8274 year: 2015 end-page: 8283 publication-title: J. Am. Chem. Soc. – volume: 33 start-page: 3499 year: 1992 end-page: 3502 publication-title: Tetrahedron Lett. – volume: 67 start-page: 5005 year: 2002 end-page: 5008 publication-title: J. Org. Chem. – volume: 126 start-page: 13906 year: 2004 end-page: 13907 publication-title: J. Am. Chem. Soc. – volume: 139 start-page: 10653 year: 2017 end-page: 10656 publication-title: J. Am. Chem. Soc. – volume: 26 start-page: 153 year: 1987 end-page: 155 publication-title: Angew. Chem. Int. Ed. – start-page: 10 year: 2018 publication-title: Chem. Sci. – volume: 45 start-page: 354 year: 2006 end-page: 366 publication-title: Angew. Chem. Int. Ed. – volume: 50 start-page: 359 year: 1994 end-page: 370 publication-title: Tetrahedron – volume: 79 start-page: 769 year: 2014 end-page: 776 publication-title: J. Org. Chem. – volume: 17 start-page: 877 year: 1987 end-page: 892 publication-title: Synth. Commun. – volume: 136 start-page: 14730 year: 2014 end-page: 14733 publication-title: J. Am. Chem. Soc. – volume: 61 start-page: 5895 year: 1996 end-page: 5904 publication-title: J. Org. Chem. – volume: 120 start-page: 11822 year: 1998 end-page: 11823 publication-title: J. Am. Chem. Soc. – start-page: 295 year: 1995 end-page: 296 publication-title: J. Chem. Soc., Chem. Commun. – volume: 45 start-page: 5263 year: 1989 end-page: 5268 publication-title: Tetrahedron – volume: 123 start-page: 5374 year: 2001 end-page: 5375 publication-title: J. Am. Chem. Soc. – volume: 2006 start-page: 3061 year: 2006 end-page: 3064 publication-title: Synlett – volume: 26 start-page: 4756 year: 2007 end-page: 4762 publication-title: Organometallics – volume: 94 start-page: 519 year: 1994 end-page: 564 publication-title: Chem. Rev. – volume: 51 start-page: 2485 year: 2012 end-page: 2488 publication-title: Angew. Chem. Int. Ed. – volume: 8 start-page: 5181 year: 2017 end-page: 5185 publication-title: Chem. Sci. – volume: 50 start-page: 403 year: 1994 end-page: 414 publication-title: Tetrahedron – volume: 71 start-page: 4413 year: 2015 end-page: 4417 publication-title: Tetrahedron – volume: 15 start-page: 46 year: 2013 end-page: 49 publication-title: Org. Lett. – volume: 53 start-page: 10733 year: 2014 end-page: 10736 publication-title: Angew. Chem. Int. Ed. – volume: 137 start-page: 13476 year: 2015 end-page: 13479 publication-title: J. Am. Chem. Soc. – volume: 2003 start-page: 2115 year: 2003 end-page: 2134 publication-title: Synthesis – volume: 346 start-page: 905 year: 2004 end-page: 908 publication-title: Adv. Synth. Catal. – volume: 48 start-page: 3146 year: 2009 end-page: 3149 publication-title: Angew. Chem. Int. Ed. – volume: 9 start-page: 904 year: 2018 end-page: 909 publication-title: Chem. Sci. – volume: 37 start-page: 2034 year: 1972 end-page: 2035 publication-title: J. Org. Chem. – volume: 50 start-page: 472 year: 2014 end-page: 474 publication-title: Chem. Commun. – volume: 38 start-page: 3242 year: 2009 end-page: 3272 publication-title: Chem. Soc. Rev. – volume: 136 start-page: 4101 year: 2014 end-page: 4104 publication-title: J. Am. Chem. Soc. – volume: 127 start-page: 8644 year: 2005 end-page: 8651 publication-title: J. Am. Chem. Soc. – volume: 133 start-page: 20146 year: 2011 end-page: 20148 publication-title: J. Am. Chem. Soc. – volume: 49 start-page: 3576 year: 2017 end-page: 3581 publication-title: Synthesis – volume: 53 start-page: 3001 year: 2014 end-page: 3005 publication-title: Angew. Chem. Int. Ed. – volume: 110 start-page: 1147 year: 2010 end-page: 1169 publication-title: Chem. Rev. – volume: 126 start-page: 10250 year: 2004 end-page: 10251 publication-title: J. Am. Chem. Soc. – volume: 60 start-page: 4007 year: 2004 end-page: 4017 publication-title: Tetrahedron – volume: 106 start-page: 2651 year: 2006 end-page: 2710 publication-title: Chem. Rev. – volume: 98 start-page: 1810 year: 1976 end-page: 1823 publication-title: J. Am. Chem. Soc. – volume: 23 start-page: 4517 year: 1982 end-page: 4520 publication-title: Tetrahedron Lett. – volume: 140 start-page: 159 year: 2018 end-page: 162 publication-title: J. Am. Chem. Soc. – volume: 139 start-page: 5700 year: 2017 end-page: 5703 publication-title: J. Am. Chem. Soc. – volume: 32 start-page: 6923 year: 1991 end-page: 6926 publication-title: Tetrahedron Lett. – volume: 53 start-page: 2386 year: 2017 end-page: 2389 publication-title: Chem. Commun. – volume: 124 start-page: 3812 year: 2002 end-page: 3813 publication-title: J. Am. Chem. Soc. – volume: 53 start-page: 2308 year: 2012 end-page: 2311 publication-title: Tetrahedron Lett. – start-page: 833 year: 1991 – volume: 116 start-page: 12133 year: 1994 end-page: 12134 publication-title: J. Am. Chem. Soc. – volume: 2 start-page: 1213 year: 2000 end-page: 1216 publication-title: Org. Lett. – volume: 67 start-page: 5860 year: 2002 end-page: 5863 publication-title: J. Org. Chem. – volume: 135 start-page: 4167 year: 2013 end-page: 4170 publication-title: J. Am. Chem. Soc. – volume: 19 start-page: 8405 year: 2013 end-page: 8410 publication-title: Chem. Eur. J. – volume: 42 start-page: 1074 year: 2009 end-page: 1086 publication-title: Acc. Chem. Res. – volume: 139 start-page: 10657 year: 2017 end-page: 10660 publication-title: J. Am. Chem. Soc. – volume: 48 start-page: 3891 year: 1992 end-page: 3902 publication-title: Tetrahedron – volume: 139 start-page: 2904 year: 2017 end-page: 2907 publication-title: J. Am. Chem. Soc. – volume: 139 start-page: 6835 year: 2017 end-page: 6838 publication-title: J. Am. Chem. Soc. – volume: 17 start-page: 2174 year: 2015 end-page: 2177 publication-title: Org. Lett. – volume: 52 start-page: 4000 year: 2013 end-page: 4003 publication-title: Angew. Chem. Int. Ed. – volume: 138 start-page: 4014 year: 2016 end-page: 4017 publication-title: J. Am. Chem. Soc. – volume: 69 start-page: 187 year: 2015 end-page: 190 publication-title: Chimia – volume: 1998 start-page: 1249 year: 1998 end-page: 1251 publication-title: Synthesis – volume: 38 start-page: 1763 year: 1997 end-page: 1766 publication-title: Tetrahedron Lett. – volume: 115 start-page: 7027 year: 1993 end-page: 7028 publication-title: J. Am. Chem. Soc. – volume: 139 start-page: 12688 year: 2017 end-page: 12695 publication-title: J. Am. Chem. Soc. – volume: 2 start-page: 1204 year: 1996 end-page: 1220 publication-title: Chem. Eur. J. – volume: 107 start-page: 8289 year: 1985 end-page: 8291 publication-title: J. Am. Chem. Soc. – volume: 54 start-page: 5250 year: 2015 end-page: 5254 publication-title: Angew. Chem. Int. Ed. – volume: 75 start-page: 2134 year: 2010 end-page: 2137 publication-title: J. Org. Chem. – volume: 133 start-page: 5784 year: 2011 end-page: 5787 publication-title: J. Am. Chem. Soc. – ident: e_1_2_6_106_1 doi: 10.1021/jacs.6b13299 – ident: e_1_2_6_51_2 doi: 10.1246/cl.1987.193 – ident: e_1_2_6_58_1 doi: 10.1002/(SICI)1521-3773(19980202)37:1/2<152::AID-ANIE152>3.0.CO;2-8 – ident: e_1_2_6_205_2 doi: 10.1021/jacs.7b12160 – ident: e_1_2_6_49_2 doi: 10.1016/0040-4020(89)80008-0 – ident: e_1_2_6_171_2 doi: 10.1016/S0040-4020(97)00754-0 – ident: e_1_2_6_155_2 doi: 10.1021/ja00312a095 – ident: e_1_2_6_62_2 doi: 10.1039/b813246a – ident: e_1_2_6_195_1 doi: 10.1016/S0040-4039(00)93407-5 – ident: e_1_2_6_18_2 doi: 10.1021/ja054754v – ident: e_1_2_6_197_1 doi: 10.1021/acs.orglett.6b00447 – ident: e_1_2_6_40_2 doi: 10.1021/jacs.7b10529 – ident: e_1_2_6_180_1 doi: 10.1055/s-2006-951508 – ident: e_1_2_6_94_2 doi: 10.1039/b306797c – ident: e_1_2_6_173_1 doi: 10.1016/j.tetlet.2012.02.096 – ident: e_1_2_6_139_2 doi: 10.1055/s-2003-42082 – ident: e_1_2_6_59_1 doi: 10.1021/ol0356643 – ident: e_1_2_6_212_2 doi: 10.1021/ja210307s – ident: e_1_2_6_79_2 doi: 10.1021/ja00437a018 – ident: e_1_2_6_202_1 – ident: e_1_2_6_123_1 doi: 10.1021/jo00977a038 – ident: e_1_2_6_224_1 doi: 10.1021/ja046810i – ident: e_1_2_6_153_1 doi: 10.1016/S0040-4020(01)80763-8 – ident: e_1_2_6_112_1 doi: 10.1021/ol200536h – ident: e_1_2_6_75_1 doi: 10.1021/ja304344h – ident: e_1_2_6_83_2 doi: 10.1002/anie.198701531 – ident: e_1_2_6_148_1 doi: 10.1016/0040-4039(95)01676-9 – ident: e_1_2_6_33_2 doi: 10.1021/jo1002032 – ident: e_1_2_6_220_1 doi: 10.1021/ja309978c – ident: e_1_2_6_114_1 doi: 10.1002/anie.200900218 – ident: e_1_2_6_91_2 doi: 10.1021/jo202221c – ident: e_1_2_6_210_1 doi: 10.1021/ja8066308 – ident: e_1_2_6_1_1 doi: 10.1021/cr00032a009 – ident: e_1_2_6_9_2 doi: 10.1021/cr100327p – ident: e_1_2_6_101_1 doi: 10.1021/ja412881j – ident: e_1_2_6_22_2 doi: 10.1021/ja8084065 – ident: e_1_2_6_93_2 doi: 10.1038/nrd2060 – ident: e_1_2_6_135_2 doi: 10.1016/S0010-8545(96)90182-4 – ident: e_1_2_6_168_2 doi: 10.1016/S0040-4020(00)01030-9 – ident: e_1_2_6_78_1 – ident: e_1_2_6_178_1 doi: 10.1021/jo025665t – ident: e_1_2_6_167_1 – ident: e_1_2_6_105_1 doi: 10.1021/ja504458j – ident: e_1_2_6_76_1 doi: 10.1021/acs.orglett.6b00517 – ident: e_1_2_6_188_2 doi: 10.1055/s-0036-1588804 – ident: e_1_2_6_70_2 doi: 10.1021/ja3110544 – ident: e_1_2_6_142_1 – ident: e_1_2_6_198_1 doi: 10.1002/anie.201607976 – ident: e_1_2_6_169_2 doi: 10.1016/S0040-4020(00)00661-X – ident: e_1_2_6_3_2 doi: 10.1002/anie.200500195 – ident: e_1_2_6_110_1 doi: 10.1021/jacs.6b10468 – ident: e_1_2_6_113_1 doi: 10.1002/anie.201511624 – ident: e_1_2_6_6_2 doi: 10.1002/9783527612222 – ident: e_1_2_6_141_1 doi: 10.1016/S0040-4020(01)90073-0 – ident: e_1_2_6_158_2 doi: 10.1021/jo00239a054 – ident: e_1_2_6_32_2 doi: 10.1021/ol049702 – ident: e_1_2_6_71_2 doi: 10.1039/C4SC03074E – ident: e_1_2_6_138_1 – start-page: 10 year: 2018 ident: e_1_2_6_68_2 publication-title: Chem. Sci. – ident: e_1_2_6_176_2 doi: 10.1021/jo960677y – ident: e_1_2_6_85_1 – ident: e_1_2_6_56_1 doi: 10.1055/s-1998-6086 – ident: e_1_2_6_8_2 – ident: e_1_2_6_213_2 doi: 10.1021/ja109686v – ident: e_1_2_6_189_1 doi: 10.1021/ja00191a066 – ident: e_1_2_6_216_2 doi: 10.1002/anie.201311009 – ident: e_1_2_6_170_1 – ident: e_1_2_6_55_2 doi: 10.1016/S0040-4039(00)92673-X – ident: e_1_2_6_74_1 doi: 10.1021/ol4023358 – ident: e_1_2_6_172_2 doi: 10.1016/S0040-4039(01)01811-1 – ident: e_1_2_6_179_1 doi: 10.1021/ja0100423 – ident: e_1_2_6_66_1 – ident: e_1_2_6_121_1 doi: 10.1021/acs.orglett.5b00775 – ident: e_1_2_6_24_2 doi: 10.1021/ja909555d – ident: e_1_2_6_184_1 – ident: e_1_2_6_187_2 doi: 10.1021/acs.orglett.6b02665 – ident: e_1_2_6_45_1 doi: 10.1021/acs.organomet.6b00532 – ident: e_1_2_6_23_2 doi: 10.1021/ja1034123 – ident: e_1_2_6_207_1 doi: 10.1021/jacs.5b10176 – ident: e_1_2_6_100_1 doi: 10.1021/ol303003g – ident: e_1_2_6_182_1 doi: 10.1002/anie.200702528 – ident: e_1_2_6_80_2 doi: 10.1021/ja045047p – ident: e_1_2_6_143_2 doi: 10.1016/S0040-4039(00)74293-6 – ident: e_1_2_6_12_2 doi: 10.1021/cr0505268 – ident: e_1_2_6_38_2 doi: 10.1021/ol4009848 – ident: e_1_2_6_48_1 – ident: e_1_2_6_117_2 doi: 10.1039/b918358b – ident: e_1_2_6_127_1 doi: 10.1021/jo0255779 – ident: e_1_2_6_4_2 doi: 10.1126/science.aaf6123 – ident: e_1_2_6_13_2 doi: 10.1002/anie.200500368 – ident: e_1_2_6_222_1 doi: 10.1016/j.tet.2015.03.012 – ident: e_1_2_6_60_1 – ident: e_1_2_6_44_2 doi: 10.1021/cr9903048 – ident: e_1_2_6_102_1 doi: 10.1021/jacs.6b09170 – ident: e_1_2_6_25_2 doi: 10.1021/ja00317a059 – ident: e_1_2_6_111_1 doi: 10.1002/tcr.10026 – ident: e_1_2_6_63_1 doi: 10.1021/ja201358b – ident: e_1_2_6_165_2 doi: 10.1016/S0040-4039(00)80814-X – ident: e_1_2_6_41_1 – ident: e_1_2_6_150_1 – ident: e_1_2_6_50_2 doi: 10.1246/bcsj.66.3522 – ident: e_1_2_6_137_1 doi: 10.1016/S0040-4039(00)96556-0 – ident: e_1_2_6_98_1 doi: 10.1021/ja054549f – ident: e_1_2_6_19_2 doi: 10.1002/anie.201600379 – ident: e_1_2_6_31_2 doi: 10.1021/ja0762240 – ident: e_1_2_6_225_1 doi: 10.1055/s-0032-1316555 – ident: e_1_2_6_131_1 – ident: e_1_2_6_28_2 doi: 10.1021/ja0460920 – ident: e_1_2_6_92_2 doi: 10.1021/jm0512903 – ident: e_1_2_6_226_1 doi: 10.1002/anie.201210250 – ident: e_1_2_6_97_1 doi: 10.1039/C7SC03149A – ident: e_1_2_6_115_1 doi: 10.1021/ol1009575 – ident: e_1_2_6_64_1 doi: 10.1021/ol502279u – ident: e_1_2_6_126_2 doi: 10.1021/ja00796a056 – ident: e_1_2_6_11_2 doi: 10.1002/anie.201107017 – ident: e_1_2_6_30_2 doi: 10.1021/jacs.5b07203 – ident: e_1_2_6_177_1 doi: 10.1021/ol0056426 – ident: e_1_2_6_67_2 doi: 10.1002/adsc.200404041 – ident: e_1_2_6_47_1 doi: 10.1016/0022-328X(84)80586-0 – ident: e_1_2_6_16_2 doi: 10.1002/anie.201402462 – ident: e_1_2_6_215_1 – ident: e_1_2_6_163_1 doi: 10.1039/c39950000295 – ident: e_1_2_6_145_1 doi: 10.1016/S0040-4039(97)00195-0 – ident: e_1_2_6_116_1 – ident: e_1_2_6_160_1 doi: 10.1021/acs.orglett.6b02154 – ident: e_1_2_6_104_1 doi: 10.1021/jacs.7b03195 – ident: e_1_2_6_128_1 – ident: e_1_2_6_183_1 doi: 10.1002/chem.201300882 – start-page: 6 year: 2016 ident: e_1_2_6_10_2 publication-title: ACS Catal. – ident: e_1_2_6_65_1 doi: 10.1021/jacs.5b08734 – ident: e_1_2_6_194_1 doi: 10.1039/b820636h – ident: e_1_2_6_95_2 doi: 10.1080/00397918708063944 – ident: e_1_2_6_214_1 doi: 10.1002/anie.201108446 – ident: e_1_2_6_15_1 – ident: e_1_2_6_196_1 doi: 10.1021/ol901799p – ident: e_1_2_6_73_1 doi: 10.1021/jacs.7b06917 – ident: e_1_2_6_203_2 doi: 10.1021/jo960617s – ident: e_1_2_6_174_1 – ident: e_1_2_6_149_1 doi: 10.1016/S0040-4039(00)73183-2 – ident: e_1_2_6_208_1 doi: 10.1021/ja500706v – ident: e_1_2_6_118_2 doi: 10.1002/open.201100010 – ident: e_1_2_6_190_1 doi: 10.1002/(SICI)1521-3773(19990517)38:10<1452::AID-ANIE1452>3.0.CO;2-P – ident: e_1_2_6_108_1 doi: 10.1016/j.jfluchem.2014.04.004 – ident: e_1_2_6_90_1 – ident: e_1_2_6_175_2 doi: 10.1021/ja00105a096 – ident: e_1_2_6_136_2 doi: 10.1021/cr00026a008 – ident: e_1_2_6_7_2 doi: 10.1016/B978-0-08-052349-1.00110-4 – ident: e_1_2_6_39_2 doi: 10.1002/anie.201303724 – ident: e_1_2_6_57_1 doi: 10.1021/jo016212b – ident: e_1_2_6_186_2 doi: 10.1039/C3CC47780K – ident: e_1_2_6_221_1 doi: 10.1021/jacs.5b04691 – ident: e_1_2_6_20_2 doi: 10.1002/anie.201500636 – ident: e_1_2_6_21_2 doi: 10.1021/jacs.6b02158 – ident: e_1_2_6_192_2 doi: 10.1016/S0040-4020(01)80760-2 – ident: e_1_2_6_5_1 – ident: e_1_2_6_2_1 – ident: e_1_2_6_27_1 – ident: e_1_2_6_42_2 doi: 10.1039/C7SC01204G – ident: e_1_2_6_120_1 doi: 10.1021/acs.orglett.5b01722 – ident: e_1_2_6_125_2 doi: 10.1021/ja00423a028 – ident: e_1_2_6_99_1 doi: 10.1021/jacs.7b06567 – ident: e_1_2_6_130_2 doi: 10.1021/om700311x – ident: e_1_2_6_223_1 doi: 10.1021/jacs.7b06191 – ident: e_1_2_6_181_1 doi: 10.1002/ejoc.201403511 – ident: e_1_2_6_26_2 doi: 10.1002/anie.201101857 – ident: e_1_2_6_140_2 doi: 10.1021/cr800420x – ident: e_1_2_6_81_2 doi: 10.1021/ja052099l – ident: e_1_2_6_46_1 doi: 10.1016/S0040-4039(00)85642-7 – ident: e_1_2_6_164_1 – ident: e_1_2_6_211_1 – ident: e_1_2_6_103_1 doi: 10.1021/ja982732l – ident: e_1_2_6_17_2 doi: 10.1021/ja3034075 – ident: e_1_2_6_87_2 doi: 10.1021/cr900184e – ident: e_1_2_6_219_1 doi: 10.1002/anie.201404802 – ident: e_1_2_6_72_1 doi: 10.1021/acs.orglett.7b01036 – ident: e_1_2_6_29_2 doi: 10.1021/ja0430346 – ident: e_1_2_6_53_1 – ident: e_1_2_6_166_2 doi: 10.1016/S0040-4020(00)00659-1 – ident: e_1_2_6_201_1 doi: 10.1021/ja00068a092 – ident: e_1_2_6_96_1 doi: 10.1002/anie.201606458 – ident: e_1_2_6_154_1 – ident: e_1_2_6_193_2 doi: 10.1016/0040-4039(95)01696-F – ident: e_1_2_6_107_1 doi: 10.1021/jo401831t – ident: e_1_2_6_124_1 – ident: e_1_2_6_144_2 doi: 10.1016/S0040-4020(01)88469-6 – ident: e_1_2_6_185_2 doi: 10.1002/chem.201200190 – ident: e_1_2_6_156_2 doi: 10.1021/ja9533196 – ident: e_1_2_6_37_2 doi: 10.1021/jo402705w – ident: e_1_2_6_69_1 – ident: e_1_2_6_84_2 doi: 10.1021/om00125a008 – ident: e_1_2_6_152_2 doi: 10.1016/j.tet.2004.03.023 – ident: e_1_2_6_109_1 doi: 10.1021/ol403263c – ident: e_1_2_6_129_2 doi: 10.1002/ejoc.200300543 – ident: e_1_2_6_218_1 doi: 10.1002/anie.201202771 – ident: e_1_2_6_122_1 doi: 10.1021/ja00763a028 – ident: e_1_2_6_151_2 doi: 10.1016/S0040-4039(96)02442-2 – ident: e_1_2_6_36_2 doi: 10.1002/anie.201002739 – ident: e_1_2_6_61_2 doi: 10.1515/pac-2014-5041 – ident: e_1_2_6_35_2 doi: 10.1002/anie.200903178 – ident: e_1_2_6_86_2 doi: 10.1039/b816707a – ident: e_1_2_6_161_1 doi: 10.1021/ja017315e – ident: e_1_2_6_200_1 doi: 10.1021/jacs.7b01922 – ident: e_1_2_6_52_1 doi: 10.1016/S0040-4020(01)81100-5 – ident: e_1_2_6_88_2 doi: 10.1021/ar9000058 – ident: e_1_2_6_133_2 doi: 10.1021/jm9806998 – ident: e_1_2_6_146_1 doi: 10.1016/j.tet.2015.06.030 – ident: e_1_2_6_159_1 doi: 10.1021/ol9900663 – ident: e_1_2_6_162_1 doi: 10.1016/0040-4039(91)80445-C – ident: e_1_2_6_217_2 doi: 10.2533/chimia.2015.187 – ident: e_1_2_6_204_2 doi: 10.1002/chem.19960021006 – ident: e_1_2_6_82_2 doi: 10.1002/anie.198707711 – ident: e_1_2_6_89_1 doi: 10.1039/C7SC04351A – ident: e_1_2_6_14_2 doi: 10.1021/cr020027w – ident: e_1_2_6_43_2 doi: 10.1021/ja2091883 – ident: e_1_2_6_209_1 doi: 10.1021/ol801168j – ident: e_1_2_6_77_1 doi: 10.1021/jacs.7b06340 – ident: e_1_2_6_132_2 doi: 10.1021/acs.chemrev.6b00833 – ident: e_1_2_6_199_1 doi: 10.1039/C6CC10075A – ident: e_1_2_6_119_2 doi: 10.1021/jo1018188 – ident: e_1_2_6_34_2 doi: 10.1021/jo0625958 – ident: e_1_2_6_54_2 doi: 10.1016/S0040-4039(00)98060-2 – ident: e_1_2_6_157_2 doi: 10.1021/ja9533205 – ident: e_1_2_6_147_1 doi: 10.1021/acs.orglett.7b00794 – ident: e_1_2_6_134_1 – ident: e_1_2_6_206_1 doi: 10.1021/ja509056j – ident: e_1_2_6_191_1 |
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| Snippet | Transition metal (TM)‐catalyzed difunctionalization of unactivated olefins with two carbon‐based entities is a powerful method to construct complex molecular... Transition metal (TM)-catalyzed difunctionalization of unactivated olefins with two carbon-based entities is a powerful method to construct complex molecular... |
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| SubjectTerms | Alkenes Carbon monoxide Cross-coupling Cyclization Dicarbofunctionalization Heck carbometallation Intermediates Nucleophiles Olefins Organic chemistry Substrates |
| Title | Transition Metal‐Catalyzed Dicarbofunctionalization of Unactivated Olefins |
| URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Ftcr.201700098 https://www.ncbi.nlm.nih.gov/pubmed/29517841 https://www.proquest.com/docview/2098771440 https://www.proquest.com/docview/2012115789 |
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