메뉴 건너뛰기




Volumn 47, Issue 35, 2008, Pages 6647-6649

Catalytic enantioselective trapping of an alcoholic oxonium ylide with aldehydes: RhII/ZrIV-co-catalyzed three-component reactions of aryl diazoacetates, benzyl alcohol, and aldehydes

Author keywords

Asymmetric catalysis; Diazo compounds; Lewis acids; Multicomponent reaction; Ylides

Indexed keywords

ACIDS; ALDEHYDES; ENANTIOSELECTIVITY; ORGANIC COMPOUNDS; RHODIUM;

EID: 53249105825     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200801510     Document Type: Article
Times cited : (80)

References (50)
  • 4
    • 84890597202 scopus 로고    scopus 로고
    • Eds, J. Zhu, H. Bienaymé, Wiley-VCH, Weinheim
    • c) Multicomponent Reactions; (Eds.: J. Zhu, H. Bienaymé), Wiley-VCH, Weinheim, 2005;
    • (2005) Multicomponent Reactions
  • 12
    • 0344861909 scopus 로고    scopus 로고
    • For articles on multicomponent reactions, see: a
    • For articles on multicomponent reactions, see: a) P. Wipf, C. R. J. Stephenson, K. Okumura, J. Am. Chem. Soc. 2003, 125, 14694;
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 14694
    • Wipf, P.1    Stephenson, C.R.J.2    Okumura, K.3
  • 18
    • 36349015033 scopus 로고    scopus 로고
    • For representative reactions for the trapping of onium ylides, see: a
    • For representative reactions for the trapping of onium ylides, see: a) Y. Wang, Y. Zhu, Z. Chen, A. Mi, W. Hu, M. Doyle, Org. Lett. 2003, 5, 3924;
    • (2003) Org. Lett , vol.5 , pp. 3924
    • Wang, Y.1    Zhu, Y.2    Chen, Z.3    Mi, A.4    Hu, W.5    Doyle, M.6
  • 25
    • 33847093544 scopus 로고    scopus 로고
    • For comprehensive references of chiral Lewis acid catalyzed reactions, see: a, Ed, R. Mahrwald, Wiley-VCH, Weinheim
    • For comprehensive references of chiral Lewis acid catalyzed reactions, see: a) Modern Aldol Reactions, Vols. 1 and 2 (Ed.: R. Mahrwald), Wiley-VCH, Weinheim, 2004;
    • (2004) Modern Aldol Reactions, Vols. 1 and 2
  • 26
    • 0003441987 scopus 로고    scopus 로고
    • Ed, H. Yamamoto, Oxford University Perss, Oxford
    • b) Lewis Acid Reagents-A Practial Approach (Ed.: H. Yamamoto), Oxford University Perss, Oxford, 1999;
    • (1999) Lewis Acid Reagents-A Practial Approach
  • 27
    • 53249120908 scopus 로고    scopus 로고
    • for asymmetric aldol reactions, see: M. Sauamura, Y. Ito in Catalytic Asymmetric Synthesis (Ed.: I. Ojima), VCH, New York, 1993, Chapter 8B1, pp. 493-512;
    • c) for asymmetric aldol reactions, see: M. Sauamura, Y. Ito in Catalytic Asymmetric Synthesis (Ed.: I. Ojima), VCH, New York, 1993, Chapter 8B1, pp. 493-512;
  • 28
    • 53249095387 scopus 로고    scopus 로고
    • for recent advances in asymmetric aldol addition reactions, see: E. M. Carreira in Catalytic Asymmetric Synthesis (Ed.: I. Ojima), VCH, New York, 1993, Chapter 8B2, pp. 513-541;
    • d) for recent advances in asymmetric aldol addition reactions, see: E. M. Carreira in Catalytic Asymmetric Synthesis (Ed.: I. Ojima), VCH, New York, 1993, Chapter 8B2, pp. 513-541;
  • 34
    • 10844266525 scopus 로고    scopus 로고
    • Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Heidelberg
    • a) S. Kobayashi, M. Ueno in Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Heidelberg, 1999, suppl. 1, p. 143-150;
    • (1999) Comprehensive Asymmetric Catalysis , Issue.SUPPL. 1 , pp. 143-150
    • Kobayashi, S.1    Ueno, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.