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Volumn 133, Issue 23, 2011, Pages 8972-8981

Asymmetric Rh(II)-catalyzed cyclopropanation of alkenes with diacceptor diazo compounds: P -methoxyphenyl ketone as a general stereoselectivity controlling group

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVES; CARBENES; CATALYTIC AMOUNTS; CYCLOPROPANATION; DIASTEREO- AND ENANTIOSELECTIVITY; DIAZO COMPOUNDS; ENANTIOPURE; LEWIS BASIS; MECHANISTIC STUDIES; STEREO-SELECTIVE;

EID: 79958829858     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja201237j     Document Type: Article
Times cited : (150)

References (64)
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    • For selected reviews on the use of electrophilic cyclopropanes in organic synthesis, see
    • For selected reviews on the use of electrophilic cyclopropanes in organic synthesis, see: Campbell, M. J.; Johnson, J. S.; Parsons, A. T.; Pohlhaus, P. D.; Sanders, S. D. J. Org. Chem. 2010, 75, 6317-6325
    • (2010) J. Org. Chem. , vol.75 , pp. 6317-6325
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  • 12
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    • For recent examples of nucleophilic addition on enantioenriched electrophilic cyclopropanes and its application in natural product synthesis, see
    • For recent examples of nucleophilic addition on enantioenriched electrophilic cyclopropanes and its application in natural product synthesis, see: Marcoux, D.; Goudreau, S. R.; Charette, A. B. J. Org. Chem. 2009, 74, 8939-8955
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    • Marcoux, D.1    Goudreau, S.R.2    Charette, A.B.3
  • 16
    • 28044450635 scopus 로고    scopus 로고
    • For selected examples of formal cycloadditions on enantioenriched electrophilic cyclopropanes and its application in natural product synthesis, see
    • For selected examples of formal cycloadditions on enantioenriched electrophilic cyclopropanes and its application in natural product synthesis, see: Pohlhaus, P. D.; Johnson, J. S. J. Am. Chem. Soc. 2005, 127, 16014-16015
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 16014-16015
    • Pohlhaus, P.D.1    Johnson, J.S.2
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    • For asymmetric Rh(II)-catalyzed cyclopropanations with carbene precursors bearing geminal electron-withdrawing groups, see ref 3a and
    • For asymmetric Rh(II)-catalyzed cyclopropanations with carbene precursors bearing geminal electron-withdrawing groups, see ref 3a and Lindsay, V. N. G.; Lin, W.; Charette, A. B. J. Am. Chem. Soc. 2009, 131, 16383-16385
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 16383-16385
    • Lindsay, V.N.G.1    Lin, W.2    Charette, A.B.3
  • 30
    • 29844434876 scopus 로고    scopus 로고
    • For other asymmetric metal-catalyzed cyclopropanations with carbene precursors bearing geminal electron-withdrawing groups, see the following. With Cu(I):;, With Co(II):;; Angew. Chem., Int. Ed. 2008, 47, 8460-8463
    • For other asymmetric metal-catalyzed cyclopropanations with carbene precursors bearing geminal electron-withdrawing groups, see the following. With Cu(I): Moreau, B.; Charette, A. B. J. Am. Chem. Soc. 2005, 127, 18014-18015 With Co(II): Zhu, S.; Perman, J. A.; Zhang, X. P. Angew. Chem., Int. Ed. 2008, 47, 8460-8463
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 18014-18015
    • Moreau, B.1    Charette, A.B.2    Zhu, S.3    Perman, J.A.4    Zhang, X.P.5
  • 41
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    • For selected examples and reviews on asymmetric reactions using other chiral Rh(II)-carboxylate catalysts, see
    • For selected examples and reviews on asymmetric reactions using other chiral Rh(II)-carboxylate catalysts, see: Grimster, N.; Zhang, L.; Fokin, V. V. J. Am. Chem. Soc. 2010, 132, 2510-2511
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 2510-2511
    • Grimster, N.1    Zhang, L.2    Fokin, V.V.3
  • 64
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    • 2O for catalyst complexation in the reaction conditions. See Supporting Information.
    • 2O for catalyst complexation in the reaction conditions. See Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.