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Volumn 29, Issue 46, 1988, Pages 5889-5891

Enantioselective α-selenenylation of 2-phenylpropanal

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0001136770     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)82217-0     Document Type: Article
Times cited : (27)

References (23)
  • 13
    • 84987577779 scopus 로고
    • Asymmetric Synthesis with Organo-Selenium Compounds: A Facile Entry to Optically Active 4-Substituted 2-Cyclohexenones by Asymmetric Selenenylation of Ketones with Chiral Selenenamides
    • (1985) Synthesis , pp. 635
    • Hiroi1    Sato2
  • 14
    • 84918468967 scopus 로고    scopus 로고
    • 3): 1.64 (s,3H), 7.2–7.7 (m,5H) 9.76 (s,1H) 4b[[Truncated]]
  • 17
    • 27944507935 scopus 로고
    • In this paper, the optically active (+) and (−) 2-chloro 2-phenyl propanal 6 are also described.Nevertheless, the (−) aldehyde is reported to be oxidized into the (−) acid, while in our hands, it gives the (+) enantiomer. This discrepancy was due to a typographical error confirmed by a private communication from Professor R.D. Bach.
    • (1979) J. Org. Chem. , vol.44 , pp. 3168
    • Domagala1    Bach2
  • 18
    • 84918468966 scopus 로고    scopus 로고
    • C. Paulmier, F. Outurquin and J.C. Plaquevent, accompanying paper.
  • 22
    • 84918468965 scopus 로고    scopus 로고
    • 17


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.