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Volumn , Issue 18, 2011, Pages 2697-2700

A highly efficient conversion of a simple derivative of the amino acid proline into a nearly enantiomerically pure n-protected allyl amine: Use of thionyl chloride to promote the Peterson olefination

Author keywords

allylamines; amino acids; chiral pool; olefination; pyrrolidines

Indexed keywords

ALDEHYDE; ALKENE; ALLYLAMINE DERIVATIVE; BETA HYDROXYSILANE; CARBOXYLIC ACID DERIVATIVE; CHLORIDE; GRIGNARD REAGENT; PROLINE; PYRROLIDINE DERIVATIVE; SILANE DERIVATIVE; TERT BUTYL 2 [1 HYDROXY(TRIMETHYLSILYL)ETHYL]PYRROLIDINE 1 CARBOXYLATE; TERT BUTYL 2 VINYLPYRROLIDINE 1 CARBOXYLATE; THIONYL CHLORIDE; UNCLASSIFIED DRUG; VINYLPYRROLIDINE;

EID: 80455160072     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1289536     Document Type: Article
Times cited : (4)

References (35)
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    • references cited therein
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    • University of Pittsburgh USA
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    • Zhao, Y.1
  • 27
    • 0002974335 scopus 로고
    • For a review of Peterson olefination, see:, Ager D J., Org. React. 1990 38 1
    • (1990) Org. React. , vol.38 , pp. 1
    • Ager, D.J.1
  • 29
    • 64249147751 scopus 로고    scopus 로고
    • references cited therein
    • Creary X, Kochly E D., J. Org. Chem. 2009 74 2134; and references cited therein
    • (2009) J. Org. Chem. , vol.74 , pp. 2134
    • Creary, X.1    Kochly, E.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.