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Volumn 9, Issue 25, 2007, Pages 5171-5174

New method for chloroamidation of olefins. Application in the synthesis of N-glycopeptides and anticancer agents

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; ANTINEOPLASTIC AGENT; CHLORAMINE DERIVATIVE; GLYCOPEPTIDE;

EID: 37249018997     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702097q     Document Type: Article
Times cited : (50)

References (57)
  • 1
    • 0000836416 scopus 로고
    • Trost, B. M, Fleming, I, Eds, Pergamon: Oxford, England
    • Kemp, J. E. G. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, England, 1991; Vol. 3, pp 471-513.
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 471-513
    • Kemp, J.E.G.1
  • 48
    • 16844373916 scopus 로고    scopus 로고
    • Int. Ed, and references cited therein
    • (d) Reddy, B. G.; Vankar, Y. D. Angew. Chem., Int. Ed. 2005, 44, 2001 and references cited therein.
    • (2001) Angew. Chem , vol.44
    • Reddy, B.G.1    Vankar, Y.D.2
  • 51
    • 37249037766 scopus 로고    scopus 로고
    • Trans stereochemistry of the cyclohexene derivative 6 was confirmed by comparison of its spectral data as well as its M.P.
    • Trans stereochemistry of the cyclohexene derivative 6 was confirmed by comparison of its spectral data as well as its M.P.
  • 52
    • 37249075670 scopus 로고    scopus 로고
    • CCDC 651000 (9), 651048 (10), 651049 (15), 651050 (21), 651051 (22), 651052 (25) contains the supplementary crystallographic data available free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
    • CCDC 651000 (9), 651048 (10), 651049 (15), 651050 (21), 651051 (22), 651052 (25) contains the supplementary crystallographic data available free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
  • 53
    • 33645919628 scopus 로고    scopus 로고
    • Stereochemistry was confirmed by comparing the J values of related structures from the following references. (We are thankful to one of the referees for suggesting to establish the stereochemistry of furano sugar derivatives by this comparison.) (a) Liautard, V.; Desvergnes, V.; Martin, O. R. Org. Lett. 2006, 8, 1299.
    • Stereochemistry was confirmed by comparing the J values of related structures from the following references. (We are thankful to one of the referees for suggesting to establish the stereochemistry of furano sugar derivatives by this comparison.) (a) Liautard, V.; Desvergnes, V.; Martin, O. R. Org. Lett. 2006, 8, 1299.
  • 55
    • 37249090463 scopus 로고    scopus 로고
    • The N-glycosyl amides are chemically very stable. We here report for the first time that 1-N acetyl sugar derivatives can be successfully deprotected to free amines.
    • The N-glycosyl amides are chemically very stable. We here report for the first time that 1-N acetyl sugar derivatives can be successfully deprotected to free amines.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.