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Volumn 44, Issue 17, 1988, Pages 5333-5342

Asymmetric synthesis of α-amino acids by alkylation of N-[N-bis-(methylthio)methyleneglycyl]-2,5-bis(methoxymethoxymethyl)pyrrolidine and enantioselective synthesis of protected (2S,9S)-2-amino-8-oxo-9,10-epoxydecanoic acid

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Indexed keywords


EID: 0000189306     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)86040-3     Document Type: Article
Times cited : (59)

References (44)
  • 10
    • 84912832991 scopus 로고
    • Asymmetric synthesis of α-substituted amino acids and amines by carbon–carbon bond formation in position α to the nitrogen
    • (1983) Liebigs Annalen der Chemie , pp. 1668
    • Kolb1    Barth2
  • 22
    • 84914333688 scopus 로고
    • Metallierte Stickstoff-Derivate der Kohlensäure in der organischen Synthese, XIII. Selektive Mono- und Dialkylierung vonN-[Bis(alkylthio)-methylen]glycin-ethylestern zum Aufbau von kettenverlängerten und α-verzweigten α-Aminosäureestern
    • (1979) Liebigs Annalen der Chemie , pp. 2066
    • Hoppe1    Beckmann2
  • 25
    • 0022490196 scopus 로고
    • Recently Evans and Weber reported that the stannous enolate derived from the chiral glycine imide underwent a highly syn-selective aldol condensation with aldehydes
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 6757
    • Evans1    Weber2
  • 39
    • 84918140424 scopus 로고    scopus 로고
    • C9 asymmetric carbons in 18 and 19 are designated by R and S, respectively, according to Cahn-Ingold-Prelog rule, though the configuration of C9 carbons have not changed through the conversion of 18 to 19.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.