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Volumn , Issue 33, 2009, Pages 5012-5014

Highly stereoselective intramolecular α-arylation of self-stabilized non-racemic enolates: Synthesis of α-quaternary α-amino acid derivatives

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA AMINO ACID; AMINO ACID DERIVATIVE; NITROBENZENE DERIVATIVE; SULFUR DIOXIDE;

EID: 68749095949     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b910326k     Document Type: Article
Times cited : (31)

References (53)
  • 50
    • 0033524774 scopus 로고    scopus 로고
    • The use of methyl N-(p-nosyl)-phenylalaninate instead of 1a, gave the rearranged methyl N-allyl-α-(4-nitrophenyl)-phenylalaninate in 80% yield, but with an enantiomeric excess of only 19%, therefore the use of tert-butyl esters is essential for the enantioselectivity of this process
    • M. W. Wilson S. E. Ault-Justus J. C. Hodges J. R. Rubin Tetrahedron 1999 55 1647
    • (1999) Tetrahedron , vol.55 , pp. 1647
    • Wilson, M.W.1    Ault-Justus, S.E.2    Hodges, J.C.3    Rubin, J.R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.