Synthesis of Substituted Naphtho‐Ferrocenes via a Gold(I)‐Catalyzed Intramolecular 6‐endo‐Dig Cyclization
A novel series of naphtho‐ferrocene derivatives were synthesized in high yields by an efficient gold‐catalyzed intramolecular 6‐endo‐dig cyclization strategy. The salient features of this reaction include easy operation, broad substrate scope, high yields, mild conditions and it works well in wet so...
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| Published in | Chinese journal of chemistry Vol. 35; no. 6; pp. 849 - 852 |
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| Main Authors | , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Weinheim
WILEY-VCH Verlag GmbH & Co. KGaA
01.06.2017
Wiley Wiley Subscription Services, Inc |
| Subjects | |
| Online Access | Get full text |
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| Abstract | A novel series of naphtho‐ferrocene derivatives were synthesized in high yields by an efficient gold‐catalyzed intramolecular 6‐endo‐dig cyclization strategy. The salient features of this reaction include easy operation, broad substrate scope, high yields, mild conditions and it works well in wet solvent under air at room temperature.
A novel series of naphtho‐ferrocene derivatives were synthesized by a classical and efficient gold‐catalyzed intramolecular cyclization strategy. This reaction is easy to handle, with broad scope and in quantitative yield, and it works well in wet solvent under air. |
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| AbstractList | A novel series of naphtho‐ferrocene derivatives were synthesized in high yields by an efficient gold‐catalyzed intramolecular 6‐
endo
‐dig cyclization strategy. The salient features of this reaction include easy operation, broad substrate scope, high yields, mild conditions and it works well in wet solvent under air at room temperature. A novel series of naphtho-ferrocene derivatives were synthesized in high yields by an efficient gold-catalyzed intramolecular 6-endo-dig cyclization strategy. The salient features of this reaction include easy operation, broad substrate scope, high yields, mild conditions and it works well in wet solvent under air at room temperature. A novel series of naphtho‐ferrocene derivatives were synthesized in high yields by an efficient gold‐catalyzed intramolecular 6‐endo‐dig cyclization strategy. The salient features of this reaction include easy operation, broad substrate scope, high yields, mild conditions and it works well in wet solvent under air at room temperature. A novel series of naphtho‐ferrocene derivatives were synthesized by a classical and efficient gold‐catalyzed intramolecular cyclization strategy. This reaction is easy to handle, with broad scope and in quantitative yield, and it works well in wet solvent under air. |
| Author | Zhang, Junliang Wang, Yidong Zhang, Pei‐Chao Qian, Deyun Li, Wenbo |
| Author_xml | – sequence: 1 givenname: Pei‐Chao surname: Zhang fullname: Zhang, Pei‐Chao organization: East China Normal University – sequence: 2 givenname: Yidong surname: Wang fullname: Wang, Yidong organization: East China Normal University – sequence: 3 givenname: Deyun surname: Qian fullname: Qian, Deyun organization: East China Normal University – sequence: 4 givenname: Wenbo surname: Li fullname: Li, Wenbo organization: East China Normal University – sequence: 5 givenname: Junliang surname: Zhang fullname: Zhang, Junliang email: jlzhang@chem.ecnu.edu.cn organization: Chinese Academy of Sciences |
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| CitedBy_id | crossref_primary_10_1002_cjoc_201900478 crossref_primary_10_1038_s41467_021_24678_5 crossref_primary_10_1016_j_jorganchem_2018_01_016 crossref_primary_10_1016_j_rechem_2023_101131 crossref_primary_10_1016_j_tetlet_2022_153821 crossref_primary_10_1021_acs_joc_8b02334 crossref_primary_10_1002_cjoc_201700575 crossref_primary_10_1070_RCR4855 crossref_primary_10_1002_ejic_202100841 crossref_primary_10_1246_cl_220011 |
| Cites_doi | 10.1039/c6qo00087h 10.1039/b306880c 10.1039/c4qo00261j 10.1002/anie.201407717 10.1021/ja306947m 10.1039/c0cs00098a 10.1021/ar400282g 10.1021/cr500691k 10.6023/A15090627 10.1039/c2cc31972a 10.1021/acs.accounts.6b00266 10.6023/cjoc201407003 10.1039/c1cs15071e 10.6023/cjoc201501020 10.1021/acs.chemrev.6b00166 10.1002/open.201500172 10.1039/c5cs00929d 10.1021/ol502520b 10.1039/c3ra40286j 10.1021/ja500444v 10.1002/anie.201107017 10.1126/science.aaf6362 10.1002/chem.200400220 10.1039/c4ra07832b 10.1039/c6cc02624a 10.1021/acs.chemrev.5b00514 10.1002/chem.200600592 10.6023/A15010063 10.1021/cr040179m 10.1002/anie.200602761 10.6023/cjoc201502027 10.1039/B316819K 10.1021/ol400332j 10.1039/b900402p 10.1039/c5cs00183h 10.1002/anie.201502548 10.1002/cjoc.201400229 10.1002/anie.201507165 10.1021/acs.chemrev.6b00181 10.1002/asia.201400133 10.6023/A15060395 10.1039/c6cc04034a 10.6023/cjoc201412009 10.1021/ja500699x 10.1021/cr0101510 10.1021/ol4005036 10.1002/cjoc.201201229 10.1055/s-0035-1561276 10.1002/anie.201201598 10.1039/c2cc32510a 10.1021/acs.chemrev.5b00005 10.1021/cr050992x 10.1021/acs.organomet.5b00730 10.1021/ja411146x 10.1039/c4cc05610h 10.1021/acs.joc.6b00825 10.1039/C4RA07832B 10.1039/C6CC04034A 10.1039/C5CS00929D 10.1002/chem.201602822 10.1039/C6CC02624A 10.1039/b316819k 10.1021/jo025962y 10.1002/anie.198607021 10.1039/C0CS00098A 10.1039/B306880C 10.1039/C4QO00261J 10.1039/C5SC01827G 10.1039/C5CS00183H 10.1039/C6QO00087H |
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| Keywords | gold(I)-catalysis ENANTIOSELECTIVE SYNTHESIS PLANAR CHIRAL FERROCENES cyclization DIASTEREO PHENANTHRENES HETEROARENES FULLERENE naphtho-ferrocenes CYCLOISOMERIZATION hydroarylation EFFICIENT PAHs-metallocenes AMIDES |
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| References | 2007 2007 2011 2012; 107 46 40 51 2012 2012 2014 2015 2015 2015 2016 2016 2016; 48 48 53 2 6 54 48 3 52 1986 2004 2004 2016; 25 104 33 116 2016 2016; 52 81 2009 2014 2015 2016; 38 9 115 49 1952 2008 2012 2013 2014 2016; 74 51 31 32 353 2014 2016; 50 5 2011 2015 2015 2016 2016 2016 2016 2002 2003 2004 2006 2012 2013 2013 2013 2015 2016; 40 73 115 45 116 116 67 10 12 134 15 15 135 73 74 2014 2014 2014 2014 2015 2015 2015 2015 2015; 136 136 16 4 34 35 35 35 35 2006 2013 2014 2015; 106 3 47 44 2015; 54 Ma, B (WOS:000379882200005) 2016; 52 Ma, XN (WOS:000341288500051) 2014; 4 Liu, F (WOS:000364444000005) 2015; 2 Seechurn, CCCJ (WOS:000304044900006) 2012; 51 Long, N. J. (000404029500009.30) 2008 Qian, DY (WOS:000345833100017) 2014; 53 Chinchilla, R (WOS:000295037400015) 2011; 40 Werner, H (WOS:000305180400004) 2012; 51 Oyama, H (WOS:000318588900009) 2013; 15 Chinchilla, R (WOS:000244895800008) 2007; 107 MUELLERWESTERHOFF, UT (WOS:A1986E042800004) 1986; 25 Zhang, M (WOS:000304605700023) 2012; 48 Hu, HX (WOS:000377257800019) 2016; 3 Aguilar, E (WOS:000380730100012) 2016; 116 Qian, DY (WOS:000305354000023) 2012; 48 Wang, Y (000404029500009.48) 2015; 2015 Gao, DW (WOS:000333947900012) 2014; 136 Ye, XJ (WOS:000338041200007) 2014; 32 Malischewski, M (WOS:000381561200035) 2016; 353 Zheng, JF (WOS:000360199200007) 2015; 73 Furstner, A (WOS:000184684500005) 2003 Zi, WW (WOS:000381438600009) 2016; 45 Wang, LP (WOS:000482137400001) 2013; 31 Yamamoto, K (WOS:000318001400005) 2013; 15 Lebedeva, MA (WOS:000363916700003) 2015; 115 Li, Y. (000404029500009.26) 2016; 22 Li, L (WOS:000353081600016) 2015; 35 Dorel, R (WOS:000361254500004) 2015; 115 Liu, SJ (WOS:000351191700026) 2015; 35 Deng, RX (WOS:000333551800007) 2014; 136 Furstner, A (WOS:000177559800064) 2002; 67 Mamane, V (WOS:000224146800020) 2004; 10 Zhang, XX (WOS:000361079900008) 2015; 35 WILKINSON, G (WOS:A1952UB41900103) 1952; 74 Shibata, T (WOS:000381236000012) 2016; 81 Baumgartner, T (WOS:000241906100008) 2006; 106 He, XM (WOS:000321203900001) 2013; 3 Carreras, J (WOS:000328865100027) 2013; 135 Nierengarten, I (WOS:000336248900001) 2014; 9 Zhang, QW (WOS:000355314100045) 2015; 54 Doucet, H (WOS:000244146500005) 2007; 46 Narita, A (WOS:000360654900015) 2015; 44 Zhao, JB (WOS:000369852300003) 2015; 73 Boorman, TC (WOS:000288609400007) 2011; 40 Atkinson, RCJ (WOS:000221961400006) 2004; 33 Falivene, L (WOS:000370451400008) 2016; 5 Boyarskiy, VP (WOS:000376824900003) 2016; 116 Carreras, J (WOS:000309566400049) 2012; 134 Lu, JP (WOS:000384038600022) 2016; 49 Wang, YD (WOS:000367723400044) 2015; 54 Albada, B (WOS:000385469400007) 2016; 116 Guldi, DM (WOS:000266411500007) 2009; 38 Takimiya, K (WOS:000336415700005) 2014; 47 Gao, DW (WOS:000362056400021) 2015; 34 Furstner, A (WOS:000241013100010) 2006; 12 Tang, M (WOS:000370776400006) 2016; 74 Wang, YF (WOS:000361079900002) 2015; 35 Zhang, S (WOS:000342343300021) 2014; 50 Zhang, YQ (WOS:000369749600004) 2016; 48 van Staveren, DR (WOS:000225757500006) 2004; 104 Liu, LT (WOS:000343526200028) 2014; 16 Urbano, A (WOS:000375624100016) 2016; 52 Zhang S. (e_1_2_1_13_1) 2014; 50 Wilkinson G. (e_1_2_1_4_1) 1952; 74 e_1_2_1_4_4 e_1_2_1_6_2 e_1_2_1_4_5 e_1_2_1_6_3 e_1_2_1_8_1 e_1_2_1_2_4 e_1_2_1_4_3 e_1_2_1_6_1 e_1_2_1_2_2 e_1_2_1_12_1 e_1_2_1_2_3 e_1_2_1_10_1 e_1_2_1_2_1 Long N. J. (e_1_2_1_4_2) 2008 e_1_2_1_6_8 e_1_2_1_6_9 e_1_2_1_6_6 e_1_2_1_6_7 e_1_2_1_4_6 e_1_2_1_6_4 e_1_2_1_8_2 Zhang M. (e_1_2_1_9_1) 2012; 48 e_1_2_1_6_5 Falivene L. (e_1_2_1_13_2) 2016; 5 e_1_2_1_9_9 e_1_2_1_6_12 e_1_2_1_6_11 e_1_2_1_6_14 e_1_2_1_6_13 e_1_2_1_6_10 e_1_2_1_5_3 e_1_2_1_7_1 e_1_2_1_5_4 e_1_2_1_7_2 e_1_2_1_3_3 e_1_2_1_5_1 e_1_2_1_3_4 e_1_2_1_5_2 e_1_2_1_3_1 e_1_2_1_6_16 e_1_2_1_11_2 e_1_2_1_3_2 e_1_2_1_6_15 e_1_2_1_11_3 e_1_2_1_6_17 e_1_2_1_11_1 e_1_2_1_7_9 e_1_2_1_9_7 e_1_2_1_9_8 e_1_2_1_7_7 e_1_2_1_9_5 e_1_2_1_11_4 e_1_2_1_7_8 e_1_2_1_9_6 e_1_2_1_7_5 e_1_2_1_9_3 e_1_2_1_7_6 e_1_2_1_9_4 e_1_2_1_7_3 e_1_2_1_7_4 e_1_2_1_9_2 |
| References_xml | – volume: 136 136 16 4 34 35 35 35 35 start-page: 4841 4472 5336 36241 4618 228 655 1399 1469 year: 2014 2014 2014 2014 2015 2015 2015 2015 2015 publication-title: J. Am. Chem. Soc. J. Am. Chem. Soc. Org. Lett. RSC Adv. Organometallics Chin. J. Org. Chem. Chin. J. Org. Chem. Chin. J. Org. Chem. Chin. J. Org. Chem. – volume: 25 104 33 116 start-page: 702 5931 313 11797 year: 1986 2004 2004 2016 publication-title: Angew. Chem., Int. Ed Chem. Rev. Chem. Soc. Rev. Chem. Rev. – volume: 107 46 40 51 start-page: 874 834 5084 5062 year: 2007 2007 2011 2012 publication-title: Chem. Rev Angew. Chem., Int. Ed Chem. Soc. Rev. Angew. Chem., Int. Ed – volume: 74 51 31 32 353 start-page: 6052 845 498 678 year: 1952 2008 2012 2013 2014 2016 publication-title: J. Am. Chem. Soc Ferrocenes: Ligands, Materials and Biomolecules Angew. Chem., Int. Ed Chin. J. Chem. Chin. J. Chem. Science – volume: 38 9 115 49 start-page: 1587 1436 1806 year: 2009 2014 2015 2016 publication-title: Chem. Soc. Rev Chem. Asian J Chem. Rev Acc. Chem. Res – volume: 54 start-page: 6918 year: 2015 publication-title: Angew. Chem., Int. Ed – volume: 40 73 115 45 116 116 67 10 12 134 15 15 135 73 74 start-page: 1910 1235 9028 22 4567 5894 8256 6264 2112 4556 7398 16753 1806 2104 18815 705 54 year: 2011 2015 2015 2016 2016 2016 2016 2002 2003 2004 2006 2012 2013 2013 2013 2015 2016 publication-title: Chem. Soc. Rev Acta Chim. Sinica Chem. Rev. Chem. Eur. J. Chem. Soc. Rev. Chem. Rev. Chem. Rev J. Org. Chem Chem. Commun. Chem. Eur. J. Chem. Eur. J J. Am. Chem. Soc. Org. Lett. Org. Lett. J. Am. Chem. Soc. Acta Chim. Sinica Acta Chim. Sinica – volume: 50 5 start-page: 60 year: 2014 2016 publication-title: Chem. Commun Chemistry Open – volume: 106 3 47 44 start-page: 4681 11334 6616 year: 2006 2013 2014 2015 publication-title: Chem. Rev RSC Adv Acc. Chem. Res Chem. Soc. Rev – volume: 52 81 start-page: 6419 6266 year: 2016 2016 publication-title: Chem. Commun. J. Org. Chem. – volume: 48 48 53 2 6 54 48 3 52 start-page: 7082 13751 221 5564 14849 512 759 9351 year: 2012 2012 2014 2015 2015 2015 2016 2016 2016 publication-title: Chem. Commun Chem. Commun. Angew. Chem., Int. Ed Org. Chem. Front. Chem. Sci. Angew. Chem., Int. Ed Synthesis Org. Chem. Front. Chem. Commun. – volume: 3 start-page: 759 year: 2016 ident: WOS:000377257800019 article-title: Enantioselective gold-catalyzed intermolecular [2+2]-cycloadditions of 3-styrylindoles with N-allenyl oxazolidinone publication-title: ORGANIC CHEMISTRY FRONTIERS doi: 10.1039/c6qo00087h contributor: fullname: Hu, HX – start-page: 2112 year: 2003 ident: WOS:000184684500005 article-title: Concise total synthesis of the aporphine alkaloid 7,7 '-bisdehydro-O-methylisopiline by an InCl3 mediated cycloisomerization reaction publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/b306880c contributor: fullname: Furstner, A – volume: 2 start-page: 221 year: 2015 ident: WOS:000364444000005 article-title: Gold(I)-catalyzed asymmetric [3+2]-cycloadditions of gamma-1-ethoxyethoxy-propiolates and aldehydes publication-title: ORGANIC CHEMISTRY FRONTIERS doi: 10.1039/c4qo00261j contributor: fullname: Liu, F – volume: 53 start-page: 13751 year: 2014 ident: WOS:000345833100017 article-title: Gold(I)-Catalyzed Highly Diastereo- and Enantioselective Alkyne Oxidation/Cyclopropanation of 1,6-Enynes publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201407717 contributor: fullname: Qian, DY – volume: 134 start-page: 16753 year: 2012 ident: WOS:000309566400049 article-title: Exploiting the pi-Acceptor Properties of Carbene-Stabilized Phosphorus Centered Trications [L3P] (3+): Applications in Pt(II) Catalysis publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja306947m contributor: fullname: Carreras, J – volume: 40 start-page: 1910 year: 2011 ident: WOS:000288609400007 article-title: Gold-mediated C-H bond functionalisation publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c0cs00098a contributor: fullname: Boorman, TC – volume: 47 start-page: 1493 year: 2014 ident: WOS:000336415700005 article-title: Organic Semiconductors Based on [1]Benzothieno[3,2-b][1]benzothiophene Substructure publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar400282g contributor: fullname: Takimiya, K – volume: 115 start-page: 9028 year: 2015 ident: WOS:000361254500004 article-title: Gold(I)-Catalyzed Activation of Alkynes for the Construction of Molecular Complexity publication-title: CHEMICAL REVIEWS doi: 10.1021/cr500691k contributor: fullname: Dorel, R – volume: 74 start-page: 54 year: 2016 ident: WOS:000370776400006 article-title: One-pot Enantioselective Multi-component Cascade Reactions for Synthesis of Chiral Functionalized Hydro-epoxyisochromenes: A Rapid Access to Molecular Complexity publication-title: ACTA CHIMICA SINICA doi: 10.6023/A15090627 contributor: fullname: Tang, M – volume: 25 start-page: 702 year: 1986 ident: WOS:A1986E042800004 article-title: [M.M]METALLOCENOPHANES - SYNTHESIS, STRUCTURE, AND PROPERTIES publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION contributor: fullname: MUELLERWESTERHOFF, UT – volume: 48 start-page: 7082 year: 2012 ident: WOS:000305354000023 article-title: Catalytic oxidation/C-H functionalization of N-arylpropiolamides by means of gold carbenoids: concise route to 3-acyloxindoles publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c2cc31972a contributor: fullname: Qian, DY – volume: 49 start-page: 1806 year: 2016 ident: WOS:000384038600022 article-title: Light-Matter Interactions in Phosphorene publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/acs.accounts.6b00266 contributor: fullname: Lu, JP – volume: 35 start-page: 228 year: 2015 ident: WOS:000351191700026 article-title: Palladium-Catalyzed Synthesis of 2-Hydroxyphenyl Vinylferrocene publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY doi: 10.6023/cjoc201407003 contributor: fullname: Liu, SJ – volume: 40 start-page: 5084 year: 2011 ident: WOS:000295037400015 article-title: Recent advances in Sonogashira reactions publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c1cs15071e contributor: fullname: Chinchilla, R – volume: 35 start-page: 1469 year: 2015 ident: WOS:000361079900008 article-title: Gold-Catalyzed Tandem Reactions of 2-Alkynyl Arylazides and Carboxylic Acids for the Synthesis of 1H-Indol-3-yl Esters publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY doi: 10.6023/cjoc201501020 contributor: fullname: Zhang, XX – volume: 116 start-page: 11797 year: 2016 ident: WOS:000385469400007 article-title: Organometallic-Peptide Bioconjugates: Synthetic Strategies and Medicinal Applications publication-title: CHEMICAL REVIEWS doi: 10.1021/acs.chemrev.6b00166 contributor: fullname: Albada, B – volume: 5 start-page: 60 year: 2016 ident: WOS:000370451400008 article-title: Mechanism of the Transmetalation of Organosilanes to Gold publication-title: CHEMISTRYOPEN doi: 10.1002/open.201500172 contributor: fullname: Falivene, L – volume: 45 start-page: 4567 year: 2016 ident: WOS:000381438600009 article-title: Recent advances in enantioselective gold catalysis publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c5cs00929d contributor: fullname: Zi, WW – volume: 16 start-page: 5336 year: 2014 ident: WOS:000343526200028 article-title: Asymmetric Synthesis of Planar Chiral Ferrocenes by Enantioselective Intramolecular C-H Arylation of N-(2-Haloaryl)ferrocenecarboxamides publication-title: ORGANIC LETTERS doi: 10.1021/ol502520b contributor: fullname: Liu, LT – volume: 3 start-page: 11334 year: 2013 ident: WOS:000321203900001 article-title: Conjugated main-group polymers for optoelectronics publication-title: RSC ADVANCES doi: 10.1039/c3ra40286j contributor: fullname: He, XM – volume: 136 start-page: 4841 year: 2014 ident: WOS:000333947900012 article-title: Enantioselective Synthesis of Planar Chiral Ferrocenes via Pd(0)-Catalyzed Intramolecular Direct C-H Bond Arylation publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja500444v contributor: fullname: Gao, DW – volume: 51 start-page: 5062 year: 2012 ident: WOS:000304044900006 article-title: Palladium-Catalyzed Cross-Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201107017 contributor: fullname: Seechurn, CCCJ – volume: 67 start-page: 6264 year: 2002 ident: WOS:000177559800064 article-title: Flexible synthesis of phenanthrenes by PtCl2-catalyzed cycloisomerization reaction publication-title: JOURNAL OF ORGANIC CHEMISTRY contributor: fullname: Furstner, A – volume: 353 start-page: 678 year: 2016 ident: WOS:000381561200035 article-title: Isolation and structural and electronic characterization of salts of the decamethylferrocene dication publication-title: SCIENCE doi: 10.1126/science.aaf6362 contributor: fullname: Malischewski, M – volume: 10 start-page: 4556 year: 2004 ident: WOS:000224146800020 article-title: Synthesis of phenanthrenes and polycyclic heteroarenes by transition-metal catalyzed cycloisomerization reactions publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.200400220 contributor: fullname: Mamane, V – volume: 4 start-page: 36241 year: 2014 ident: WOS:000341288500051 article-title: Palladium-catalyzed intramolecular Cp-H bond functionalization/arylation: an enantioselective approach to planar chiral quinilinoferrocenes publication-title: RSC ADVANCES doi: 10.1039/c4ra07832b contributor: fullname: Ma, XN – volume: 74 start-page: 2125 year: 1952 ident: WOS:A1952UB41900103 article-title: THE STRUCTURE OF IRON BIS-CYCLOPENTADIENYL publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY contributor: fullname: WILKINSON, G – volume: 52 start-page: 6419 year: 2016 ident: WOS:000375624100016 article-title: Mild access to planar-chiral ortho-condensed aromatic ferrocenes via gold(I)-catalyzed cycloisomerization of ortho-alkynylaryl ferrocenes publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c6cc02624a contributor: fullname: Urbano, A – volume: 116 start-page: 5894 year: 2016 ident: WOS:000376824900003 article-title: Alkenylation of Arenes and Heteroarenes with Alkynes publication-title: CHEMICAL REVIEWS doi: 10.1021/acs.chemrev.5b00514 contributor: fullname: Boyarskiy, VP – volume: 12 start-page: 7398 year: 2006 ident: WOS:000241013100010 article-title: Total syntheses of the tylophora alkaloids cryptopleurine, (-)-antofine, (-)-tylophorine, and (-)-ficuseptine C publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.200600592 contributor: fullname: Furstner, A – volume: 73 start-page: 1235 year: 2015 ident: WOS:000369852300003 article-title: Recent Advances in Directed Intramolecular C(sp(3))-H Amination Reactions for the Construction of Aza-heterocycles publication-title: ACTA CHIMICA SINICA doi: 10.6023/A15010063 contributor: fullname: Zhao, JB – volume: 22 year: 2016 ident: 000404029500009.26 publication-title: J. Chem. Eur. J. contributor: fullname: Li, Y. – volume: 106 start-page: 4681 year: 2006 ident: WOS:000241906100008 article-title: Organophosphorus pi-conjugated materials publication-title: CHEMICAL REVIEWS doi: 10.1021/cr040179m contributor: fullname: Baumgartner, T – volume: 46 start-page: 834 year: 2007 ident: WOS:000244146500005 article-title: Palladium-based catalytic systems for the synthesis of conjugated enynes by Sonogashira reactions and related alkynylations publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200602761 contributor: fullname: Doucet, H – volume: 35 start-page: 1399 year: 2015 ident: WOS:000361079900002 article-title: Recent Advances in Transition-Metal-Catalyzed Enantioselective Syntheses of Planar Chiral Ferrocenes publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY doi: 10.6023/cjoc201502027 contributor: fullname: Wang, YF – volume: 33 start-page: 313 year: 2004 ident: WOS:000221961400006 article-title: The syntheses and catalytic applications of unsymmetrical ferrocene ligands publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/B316819K contributor: fullname: Atkinson, RCJ – volume: 15 start-page: 1806 year: 2013 ident: WOS:000318001400005 article-title: Synthesis of [5]Helicenes with a Substituent Exclusively on the Interior Side of the Helix by Metal-catalyzed Cycloisomerization publication-title: ORGANIC LETTERS doi: 10.1021/ol400332j contributor: fullname: Yamamoto, K – volume: 38 start-page: 1587 year: 2009 ident: WOS:000266411500007 article-title: Fullerene for organic electronics publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/b900402p contributor: fullname: Guldi, DM – volume: 44 start-page: 6616 year: 2015 ident: WOS:000360654900015 article-title: New advances in nanographene chemistry publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c5cs00183h contributor: fullname: Narita, A – volume: 54 start-page: 6918 year: 2015 ident: WOS:000355314100045 article-title: Rhodium-Catalyzed Enantioselective Intramolecular CH Silylation for the Syntheses of Planar-Chiral Metallocene Siloles publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201502548 contributor: fullname: Zhang, QW – volume: 32 start-page: 498 year: 2014 ident: WOS:000338041200007 article-title: Synthesis of Ferrocene-Modified Carbon Nitride Photocatalysts by Surface Amidation Reaction for Phenol Synthesis publication-title: CHINESE JOURNAL OF CHEMISTRY doi: 10.1002/cjoc.201400229 contributor: fullname: Ye, XJ – volume: 54 start-page: 14849 year: 2015 ident: WOS:000367723400044 article-title: Highly Regio-, Diastereo-, and Enantioselective Gold(I)-Catalyzed Intermolecular Annulations with N-Allenamides at the Proximal C=C Bond publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201507165 contributor: fullname: Wang, YD – volume: 116 start-page: 8256 year: 2016 ident: WOS:000380730100012 article-title: 1,3-Dien-5-ynes: Versatile Building Blocks for the Synthesis of Carbo- and Heterocycles publication-title: CHEMICAL REVIEWS doi: 10.1021/acs.chemrev.6b00181 contributor: fullname: Aguilar, E – volume: 9 start-page: 1436 year: 2014 ident: WOS:000336248900001 article-title: Fullerene Sugar Balls: A New Class of Biologically Active Fullerene Derivatives publication-title: CHEMISTRY-AN ASIAN JOURNAL doi: 10.1002/asia.201400133 contributor: fullname: Nierengarten, I – volume: 73 start-page: 705 year: 2015 ident: WOS:000360199200007 article-title: Direct Transformation of Amides: Reductive Cycloaddition of Secondary Amides with Danishefsky Diene publication-title: ACTA CHIMICA SINICA doi: 10.6023/A15060395 contributor: fullname: Zheng, JF – volume: 52 start-page: 9351 year: 2016 ident: WOS:000379882200005 article-title: Gold-catalysed facile access to indene scaffolds via sequential C-H functionalization and 5-endo-dig carbocyclization publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c6cc04034a contributor: fullname: Ma, B – volume: 35 start-page: 655 year: 2015 ident: WOS:000353081600016 article-title: Efficient and Practical Synthesis of alpha-Amino Amides through Gold-Catalyzed Intermolecular Oxidation of Ynamides publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY doi: 10.6023/cjoc201412009 contributor: fullname: Li, L – volume: 136 start-page: 4472 year: 2014 ident: WOS:000333551800007 article-title: Palladium-Catalyzed Intramolecular Asymmetric C-H Functionalization/Cyclization Reaction of Metallocenes: An Efficient Approach toward the Synthesis of Planar Chiral Metallocene Compounds publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja500699x contributor: fullname: Deng, RX – volume: 104 start-page: 5931 year: 2004 ident: WOS:000225757500006 article-title: Bioorganometallic chemistry of ferrocene publication-title: CHEMICAL REVIEWS doi: 10.1021/cr0101510 contributor: fullname: van Staveren, DR – volume: 15 start-page: 2104 year: 2013 ident: WOS:000318588900009 article-title: Facile Synthetic Route to Highly Luminescent Sila[7]helicene publication-title: ORGANIC LETTERS doi: 10.1021/ol4005036 contributor: fullname: Oyama, H – volume: 31 start-page: 845 year: 2013 ident: WOS:000482137400001 article-title: (4-Ferrocenylethyne) phenylamine on Graphene as the Signal Amplificator to Determinate Dopamine and Acetaminophen Simultaneously publication-title: CHINESE JOURNAL OF CHEMISTRY doi: 10.1002/cjoc.201201229 contributor: fullname: Wang, LP – year: 2008 ident: 000404029500009.30 publication-title: Ferrocenes: Ligands, Materials and Biomolecules contributor: fullname: Long, N. J. – volume: 48 start-page: 512 year: 2016 ident: WOS:000369749600004 article-title: Gold(I)-Catalyzed Stereospecific [4+3]-Cycloaddition Reaction of 1-(Alk-1-ynyl)cyclopropyl Ketones with Nitrones: A Modular Entry to Enantioenriched 5,7-Fused Bicyclic Furo[3,4-d][1,2]oxazepines publication-title: SYNTHESIS-STUTTGART doi: 10.1055/s-0035-1561276 contributor: fullname: Zhang, YQ – volume: 51 start-page: 6052 year: 2012 ident: WOS:000305180400004 article-title: At Least 60 Years of Ferrocene: The Discovery and Rediscovery of the Sandwich Complexes publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201201598 contributor: fullname: Werner, H – volume: 48 start-page: 6399 year: 2012 ident: WOS:000304605700023 article-title: Gold(I)-catalyzed cyclization of 2-(1-alkynyl)-alk-2-en-1-one oximes: a facile access to highly substituted N-alkoxypyrroles publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c2cc32510a contributor: fullname: Zhang, M – volume: 115 start-page: 11301 year: 2015 ident: WOS:000363916700003 article-title: Harnessing the Synergistic and Complementary Properties of Fullerene and Transition-Metal Compounds for Nanomaterial Applications publication-title: CHEMICAL REVIEWS doi: 10.1021/acs.chemrev.5b00005 contributor: fullname: Lebedeva, MA – volume: 107 start-page: 874 year: 2007 ident: WOS:000244895800008 article-title: The sonogashira reaction: A booming methodology in synthetic organic chemistry publication-title: CHEMICAL REVIEWS doi: 10.1021/cr050992x contributor: fullname: Chinchilla, R – volume: 2015 start-page: 6 year: 2015 ident: 000404029500009.48 article-title: CT perfusion characteristics identify metastatic sites in liver publication-title: Biomed Res Int contributor: fullname: Wang, Y – volume: 34 start-page: 4618 year: 2015 ident: WOS:000362056400021 article-title: Pd-Catalyzed Highly Enantioselective Synthesis of Planar Chiral Ferrocenylpyridine Derivatives publication-title: ORGANOMETALLICS doi: 10.1021/acs.organomet.5b00730 contributor: fullname: Gao, DW – volume: 135 start-page: 18815 year: 2013 ident: WOS:000328865100027 article-title: Polycationic Ligands in Gold Catalysis: Synthesis and Applications of Extremely pi-Acidic Catalysts publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja411146x contributor: fullname: Carreras, J – volume: 50 start-page: 12084 year: 2014 ident: WOS:000342343300021 article-title: Synthesis of spiroaminals by bimetallic Au/Sc relay catalysis: TMS as a traceless controlling group publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c4cc05610h contributor: fullname: Zhang, S – volume: 81 start-page: 6266 year: 2016 ident: WOS:000381236000012 article-title: Pt-Catalyzed Enantioselective Cycloisomerization for the Synthesis of Planar-Chiral Ferrocene Derivatives publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.6b00825 contributor: fullname: Shibata, T – ident: e_1_2_1_7_4 doi: 10.1039/C4RA07832B – volume: 48 year: 2012 ident: e_1_2_1_9_1 publication-title: Chem. Commun contributor: fullname: Zhang M. – ident: e_1_2_1_4_6 doi: 10.1126/science.aaf6362 – volume: 50 year: 2014 ident: e_1_2_1_13_1 publication-title: Chem. Commun contributor: fullname: Zhang S. – ident: e_1_2_1_3_2 doi: 10.1002/asia.201400133 – ident: e_1_2_1_3_1 doi: 10.1039/b900402p – volume: 74 year: 1952 ident: e_1_2_1_4_1 publication-title: J. Am. Chem. Soc contributor: fullname: Wilkinson G. – ident: e_1_2_1_9_9 doi: 10.1039/C6CC04034A – ident: e_1_2_1_5_4 doi: 10.1021/acs.chemrev.6b00166 – ident: e_1_2_1_6_12 doi: 10.1021/ja306947m – ident: e_1_2_1_3_4 doi: 10.1021/acs.accounts.6b00266 – ident: e_1_2_1_11_1 doi: 10.1021/cr050992x – ident: e_1_2_1_6_5 doi: 10.1039/C5CS00929D – ident: e_1_2_1_12_1 – ident: e_1_2_1_6_4 doi: 10.1002/chem.201602822 – ident: e_1_2_1_4_3 doi: 10.1002/anie.201201598 – ident: e_1_2_1_9_3 doi: 10.1002/anie.201407717 – ident: e_1_2_1_2_1 doi: 10.1021/cr040179m – ident: e_1_2_1_6_15 doi: 10.1021/ja411146x – ident: e_1_2_1_8_1 doi: 10.1039/C6CC02624A – ident: e_1_2_1_5_3 doi: 10.1039/b316819k – ident: e_1_2_1_6_8 doi: 10.1021/jo025962y – ident: e_1_2_1_6_6 doi: 10.1021/acs.chemrev.5b00514 – ident: e_1_2_1_3_3 doi: 10.1021/acs.chemrev.5b00005 – ident: e_1_2_1_4_5 doi: 10.1002/cjoc.201400229 – ident: e_1_2_1_7_3 doi: 10.1021/ol502520b – ident: e_1_2_1_7_2 doi: 10.1021/ja500699x – ident: e_1_2_1_2_3 doi: 10.1021/ar400282g – ident: e_1_2_1_9_2 doi: 10.1039/c2cc31972a – ident: e_1_2_1_6_13 doi: 10.1021/ol400332j – ident: e_1_2_1_6_17 doi: 10.6023/A15090627 – volume: 5 start-page: 60 year: 2016 ident: e_1_2_1_13_2 publication-title: Chemistry Open contributor: fullname: Falivene L. – ident: e_1_2_1_11_2 doi: 10.1002/anie.200602761 – ident: e_1_2_1_5_1 doi: 10.1002/anie.198607021 – ident: e_1_2_1_6_1 doi: 10.1039/C0CS00098A – ident: e_1_2_1_10_1 doi: 10.1002/anie.201502548 – ident: e_1_2_1_7_6 doi: 10.6023/cjoc201407003 – ident: e_1_2_1_6_9 doi: 10.1039/B306880C – ident: e_1_2_1_6_14 doi: 10.1021/ol4005036 – ident: e_1_2_1_6_7 doi: 10.1021/acs.chemrev.6b00181 – ident: e_1_2_1_7_9 doi: 10.6023/cjoc201501020 – ident: e_1_2_1_9_4 doi: 10.1039/C4QO00261J – ident: e_1_2_1_11_4 doi: 10.1002/anie.201107017 – ident: e_1_2_1_6_3 doi: 10.1021/cr500691k – year: 2008 ident: e_1_2_1_4_2 publication-title: Ferrocenes: Ligands, Materials and Biomolecules contributor: fullname: Long N. J. – ident: e_1_2_1_9_6 doi: 10.1002/anie.201507165 – ident: e_1_2_1_4_4 doi: 10.1002/cjoc.201201229 – ident: e_1_2_1_6_11 doi: 10.1002/chem.200600592 – ident: e_1_2_1_5_2 doi: 10.1021/cr0101510 – ident: e_1_2_1_9_7 doi: 10.1055/s-0035-1561276 – ident: e_1_2_1_7_7 doi: 10.6023/cjoc201412009 – ident: e_1_2_1_7_1 doi: 10.1021/ja500444v – ident: e_1_2_1_8_2 doi: 10.1021/acs.joc.6b00825 – ident: e_1_2_1_9_5 doi: 10.1039/C5SC01827G – ident: e_1_2_1_6_16 doi: 10.6023/A15060395 – ident: e_1_2_1_7_8 doi: 10.6023/cjoc201502027 – ident: e_1_2_1_11_3 doi: 10.1039/c1cs15071e – ident: e_1_2_1_2_2 doi: 10.1039/c3ra40286j – ident: e_1_2_1_6_10 doi: 10.1002/chem.200400220 – ident: e_1_2_1_2_4 doi: 10.1039/C5CS00183H – ident: e_1_2_1_7_5 doi: 10.1021/acs.organomet.5b00730 – ident: e_1_2_1_9_8 doi: 10.1039/C6QO00087H – ident: e_1_2_1_6_2 doi: 10.6023/A15010063 |
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| Snippet | A novel series of naphtho‐ferrocene derivatives were synthesized in high yields by an efficient gold‐catalyzed intramolecular 6‐endo‐dig cyclization strategy.... A novel series of naphtho-ferrocene derivatives were synthesized in high yields by an efficient gold-catalyzed intramolecular 6-endo-dig cyclization strategy.... A novel series of naphtho‐ferrocene derivatives were synthesized in high yields by an efficient gold‐catalyzed intramolecular 6‐ endo ‐dig cyclization... |
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| SubjectTerms | Air temperature Chemical synthesis Chemistry Chemistry, Multidisciplinary cyclization Derivatives Ferrocenes Gold gold(I)‐catalysis hydroarylation naphtho‐ferrocenes PAHs‐metallocenes Physical Sciences Science & Technology Temperature effects |
| Title | Synthesis of Substituted Naphtho‐Ferrocenes via a Gold(I)‐Catalyzed Intramolecular 6‐endo‐Dig Cyclization |
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