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Volumn , Issue 17, 1994, Pages 1957-1958

A route to dipeptides containing β-amino-α-hydroxy acid fragments by coupling of N-Boc-β-lactams with α-amino esters. Application to the synthesis of (-)-bestatin

Author keywords

[No Author keywords available]

Indexed keywords

BESTATIN; BETA LACTAM; DIPEPTIDE; ESTER; ISOSERINE; SODIUM AZIDE;

EID: 0028076811     PISSN: 00224936     EISSN: None     Source Type: Journal    
DOI: 10.1039/C39940001957     Document Type: Article
Times cited : (45)

References (45)
  • 10
    • 0000125456 scopus 로고
    • Peptidase Inhibitors, ed. P. G. Sammes, Pergamon, Oxford
    • D. H. Rich, Peptidase Inhibitors, in Comprehensive Medicinal Chemistry, ed. P. G. Sammes, Pergamon, Oxford, 1990, vol. 2, p. 391.
    • (1990) Comprehensive Medicinal Chemistry , vol.2 , pp. 391
    • Rich, D.H.1
  • 34
    • 0001616426 scopus 로고
    • Potassium cyanide was also evaluated for this coupling reaction, but proved to be somewhat less effective than sodium azide. For nucleophilic ring opening of β-lactams with azide anion, see:
    • J. C. Galluci, D.-C. Ha and D. J. Hart, Tetrahedron, 1989, 45, 1283.With cyanide anion, see:
    • (1989) Tetrahedron , vol.45 , pp. 1283
    • Galluci, J.C.1    Ha, D.-C.2    Hart, D.J.3
  • 37
    • 0003511271 scopus 로고
    • E. Gross and J. Meienhofer, Academic, New York
    • E. Gross, J. Meienhofer, in The Peptides, ed. E. Gross and J. Meienhofer, Academic, New York, 1979, vol. 1, p. 1;.
    • (1979) The Peptides , vol.1 , pp. 1
    • Gross, E.1    Meienhofer, J.2
  • 45
    • 0000467936 scopus 로고
    • After completion of this work, a communication dealing with this subject has recently appeared, see:
    • I. Ojima, C. M. Sun and Y. H. Park, J. Org. Chem., 1994, 59, 1249.
    • (1994) J. Org. Chem. , vol.59 , pp. 1249
    • Ojima, I.1    Sun, C.M.2    Park, Y.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.