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Volumn 7, Issue 3, 2009, Pages 527-536

Stereoselective functionalisation of cis- and trans-2-ferrocenyl-3- pivaloyl-4-alkyl-1,3-oxazolidin-5-ones: Asymmetric synthesis of (R)- and (S)-2-alkyl-2-aminopent-4-enoic acids and (2R,3S)-2-amino-2-methyl-3-hydroxy-3- phenylpropanoic acid

Author keywords

[No Author keywords available]

Indexed keywords

ACIDS; ALDEHYDES; AMINATION; AMINES; HYDROLYSIS;

EID: 58849087131     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b814453b     Document Type: Article
Times cited : (5)

References (56)
  • 3
    • 0001521888 scopus 로고
    • For a review, see:
    • K. Fuji Chem. Rev. 1993 93 2037
    • (1993) Chem. Rev. , vol.93 , pp. 2037
    • Fuji, K.1
  • 46
    • 0001099125 scopus 로고
    • O-Pivaloyl ester 21 presumably arises by a mechanism involving initial hydrolysis of the TBDMS group and neighbouring group participation from the ferrocenyl group to give an intermediate N-acyliminium cation. N- to O-pivaloyl transfer and subsequent imine hydrolysis generates O-pivaloyl ester 21
    • D. Blaser S. Y. Ko D. Seebach J. Org. Chem. 1991 56 6230
    • (1991) J. Org. Chem. , vol.56 , pp. 6230
    • Blaser, D.1    Ko, S.Y.2    Seebach, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.