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Volumn 9, Issue 20, 2007, Pages 3881-3884

A new method for the synthesis of chiral β-branched α-amino acids

Author keywords

[No Author keywords available]

Indexed keywords


EID: 35048895719     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol071305m     Document Type: Article
Times cited : (26)

References (51)
  • 17
    • 0004246896 scopus 로고    scopus 로고
    • Krause, N, Ed, WileyVCH: Weinheim, Germany
    • (b) Breit, B.; Demel, P. In Modern Organocopper Chemistry; Krause, N., Ed.; WileyVCH: Weinheim, Germany, 2002; pp 188-223.
    • (2002) Modern Organocopper Chemistry , pp. 188-223
    • Breit, B.1    Demel, P.2
  • 22
    • 33748541824 scopus 로고    scopus 로고
    • For a review on the progress in enantioselective catalysis with chiral copper catalysts see
    • (e) For a review on the progress in enantioselective catalysis with chiral copper catalysts see: Yorimitsu, H.; Oshima, K. Angew. Chem. 2005, 117, 4509;
    • (2005) Angew. Chem , vol.117 , pp. 4509
    • Yorimitsu, H.1    Oshima, K.2
  • 23
    • 22744436808 scopus 로고    scopus 로고
    • Angew. Chem., Int. Ed. 2005, 44, 4435-4439.
    • (2005) Chem., Int. Ed , vol.44 , pp. 4435-4439
    • Angew1
  • 24
    • 35048841346 scopus 로고    scopus 로고
    • N2 product is formed preferentially.
    • N2 product is formed preferentially.
  • 40
    • 0001692317 scopus 로고    scopus 로고
    • So far only two reports have addressed stereoinduction from a stereocenter located in δ-position relative to the leaving group of an allylic substrate, a Arai, M, Kawasuji, T, Nakamura, E. J. Org. Chem. 1993, 58, 5121
    • So far only two reports have addressed stereoinduction from a stereocenter located in δ-position relative to the leaving group of an allylic substrate, (a) Arai, M.; Kawasuji, T.; Nakamura, E. J. Org. Chem. 1993, 58, 5121.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.