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Volumn , Issue 9, 1998, Pages 1321-1326

Application of the asymmetric chelate enolate Claisen rearrangement to the synthesis of unsaturated polyhydroxylated amino acids

Author keywords

Allylic esters; Chelates; Claisen rearrangements; Enolates; Unsaturated amino acids

Indexed keywords

AMINO ACID DERIVATIVE;

EID: 0031706012     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1998-6104     Document Type: Article
Times cited : (59)

References (45)
  • 25
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    • Trost, B. M.; Fleming, I.; Paquette, L. A., Eds.; Pergamon: Oxford
    • Wipf, P. In Comprehensive Organic Synthesis, Vol 5; Trost, B. M.; Fleming, I.; Paquette, L. A., Eds.; Pergamon: Oxford, 1991; p 827.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 827
    • Wipf, P.1
  • 26
    • 0008823472 scopus 로고
    • Mulzer, J.; Altenbach, H.-J.; Braun, M.; Krohn, K.; Reissig H.-U., Eds.; VCH: Weinheim
    • Altenbach H. In Organic Synthesis Highlights; Mulzer, J.; Altenbach, H.-J.; Braun, M.; Krohn, K.; Reissig H.-U., Eds.; VCH: Weinheim, 1991; pp 111, 116.
    • (1991) Organic Synthesis Highlights , pp. 111
    • Altenbach, H.1
  • 28
    • 0001377606 scopus 로고    scopus 로고
    • Helmchen, G.; Hoffmann, R. W.; Mulzer, J.; Schaumann, E., Eds.; Thieme: Stuttgart
    • Frauenrath, H. In Houben-Weyl, 4th ed., Vol. E21; Helmchen, G.; Hoffmann, R. W.; Mulzer, J.; Schaumann, E., Eds.; Thieme: Stuttgart, 1996; p 3301 and references cited therein.
    • (1996) Houben-Weyl, 4th Ed. , vol.21 E , pp. 3301
    • Frauenrath, H.1
  • 39
    • 34548198351 scopus 로고    scopus 로고
    • Because the chiral center of the amino acid is destroyed during enolate formation, racemic amino acids were used
    • Because the chiral center of the amino acid is destroyed during enolate formation, racemic amino acids were used.
  • 45
    • 34548197249 scopus 로고    scopus 로고
    • For analytical purposes a mixture of stereoisomers was obtained by rearrangement of the corresponding esters of racemic or epimeric allylic alcohols
    • For analytical purposes a mixture of stereoisomers was obtained by rearrangement of the corresponding esters of racemic or epimeric allylic alcohols.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.