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Volumn 74, Issue 15, 2009, Pages 5683-5686

P(i-PrNCH2CH2)3N as a Lewis base catalyst for the synthesis of β-hydroxynitriles using TMSAN

Author keywords

[No Author keywords available]

Indexed keywords

CATALYST LOADINGS; EFFICIENT CATALYSTS; LEWIS BASE; MILD REACTION CONDITIONS; PRODUCT YIELDS;

EID: 68049105280     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo900814t     Document Type: Article
Times cited : (36)

References (59)
  • 1
    • 68049091405 scopus 로고
    • Trost, B. M, Ed, Pergamon Press: Oxford
    • Comprehensive Organic Synthesis; Trost, B. M., Ed.; Pergamon Press: Oxford, 1991; Vol. 2, pp 1-502.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 1-502
  • 4
    • 68049107750 scopus 로고    scopus 로고
    • Fülocombining double acute accentp, F.; Huber, I.; Bernáth, G.; Hocombining double acute accentnig, H.; Senger-Wasserthal, P. Synthesis 1991, 43-46.
    • (c) Fülocombining double acute accentp, F.; Huber, I.; Bernáth, G.; Hocombining double acute accentnig, H.; Senger-Wasserthal, P. Synthesis 1991, 43-46.
  • 39
    • 68049111928 scopus 로고    scopus 로고
    • For reviews on proazaphosphatrane chemistry, see: (a) Verkade, J. G. New Aspects of Phosphorus Chemistry II. In Top. Curr. Chem. Majoral, J. P., Ed. 2002, 233, 1-44.
    • For reviews on proazaphosphatrane chemistry, see: (a) Verkade, J. G. New Aspects of Phosphorus Chemistry II. In Top. Curr. Chem. Majoral, J. P., Ed. 2002, 233, 1-44.
  • 53
    • 68049103601 scopus 로고    scopus 로고
    • Proazaphosphatranes 1a, 1c, and 1d are commercially available.
    • Proazaphosphatranes 1a, 1c, and 1d are commercially available.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.