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Volumn 346, Issue 9-10, 2004, Pages 1147-1168

The use of N-Alkyl-2,2′-bipyrrolidine derivatives as organocatalysts for the asymmetric michael addition of ketones and aldehydes to nitroolefins

Author keywords

Amines; Asymmetric catalysis; Conjugate addition; Nitroolefins; Organocatalysis

Indexed keywords

ALDEHYDE DERIVATIVE; ALKENE DERIVATIVE; ENAMINE; HYDROGEN; HYDROXYL GROUP; KETONE DERIVATIVE; NITROGEN; PYRROLIDINE DERIVATIVE;

EID: 5144224358     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/adsc.200404037     Document Type: Article
Times cited : (261)

References (132)
  • 100
    • 0003280270 scopus 로고
    • Conjugate Addition Reaction in Organic Synthesis
    • Pergamon Press: Oxford
    • P. Perlmutter, Conjugate Addition Reaction in Organic Synthesis, Tetrahedron Organic Chemistry Series 9; Pergamon Press: Oxford, 1992.
    • (1992) Tetrahedron Organic Chemistry Series , vol.9
    • Perlmutter, P.1
  • 119
    • 5144224548 scopus 로고    scopus 로고
    • note
    • New experiments have revealed a problem with the optical purity of some crops of our chiral diamines used in our previous article, which was only 89% ee. Results reported in this article have been done again with optically pure diamine.
  • 125
    • 5144232970 scopus 로고    scopus 로고
    • note
    • 3, ωR = 0.030, ωR = 0.031.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.