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Volumn 7, Issue 6, 1996, Pages 1783-1788

A two-step asymmetric synthesis of pure trans-(R,R)-diaryl-epoxides

Author keywords

[No Author keywords available]

Indexed keywords

EPOXIDE;

EID: 0042523205     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/0957-4166(96)00213-3     Document Type: Article
Times cited : (83)

References (23)
  • 5
    • 84917799098 scopus 로고
    • Ed. Allinger N.L. and Eliel E.L, Wiley-Interscience
    • Berti G. "Topics in stereochemistry" Ed. Allinger N.L. and Eliel E.L, Wiley-Interscience, 1973, vol. 7, p. 221-228.
    • (1973) Topics in Stereochemistry , vol.7 , pp. 221-228
    • Berti, G.1
  • 7
    • 0038221284 scopus 로고
    • An attempt to prepare enantiomerically enriched diaryl-epoxides from chiral arsonium ylides led to ∼41% e.e. (Allen D.G. ; Wild S.B. Organometallics 1983, 2, 394.)
    • (1983) Organometallics , vol.2 , pp. 394
    • Allen, D.G.1    Wild, S.B.2
  • 22
    • 85030199754 scopus 로고    scopus 로고
    • note
    • Racemic epoxides 4a and 4c were purchased from Aldrich while racemic epoxides 4b, 4d and 4e have been prepared through addition of the corresponding aldehydes to benzyl-dimethyl sulfonium bromide.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.