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Volumn 72, Issue 25, 2007, Pages 9753-9756

Glycosylated N-sulfonylamidines: Highly efficient copper-catalyzed multicomponent reaction with sugar alkynes, sulfonyl azides, and amines

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNES; MULTICOMPONENT REACTION; SULFONYL AZIDES;

EID: 36849073168     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo701565m     Document Type: Article
Times cited : (35)

References (27)
  • 1
    • 17144364214 scopus 로고    scopus 로고
    • Nicolaou, K. C, Hanko, R, Hartwig, W, Eds, Wiley-VCH: Weinheim, Germany, Chapter 23
    • Tuch, A.; Wallé, S. In Handbook of Combinatorial Chemistry; Nicolaou, K. C., Hanko, R., Hartwig, W., Eds.; Wiley-VCH: Weinheim, Germany, 2002; Vol. 2, Chapter 23.
    • (2002) Handbook of Combinatorial Chemistry , vol.2
    • Tuch, A.1    Wallé, S.2
  • 3
    • 0000582505 scopus 로고
    • Patai, S, Rappoport, Z, Eds, Wiley: New York, Chapter 8
    • (b) Boyd, G. V. In The Chemistry of Amidines and Imidates; Patai, S., Rappoport, Z., Eds.; Wiley: New York, 1991; Vol. 2, Chapter 8.
    • (1991) The Chemistry of Amidines and Imidates , vol.2
    • Boyd, G.V.1
  • 13
    • 33947493431 scopus 로고    scopus 로고
    • For Cu-catalyzed cycloaddition reactions see: a
    • For Cu-catalyzed cycloaddition reactions see: (a) Dedola, S.; Nepogodiev, S. A.; Field, R. A. Org. Biomol. Chem. 2007, 7, 1006-1017.
    • (2007) Org. Biomol. Chem , vol.7 , pp. 1006-1017
    • Dedola, S.1    Nepogodiev, S.A.2    Field, R.A.3
  • 18
    • 33746191914 scopus 로고    scopus 로고
    • For Cu-catalyzed MCRs with sulfonyl azides see: a
    • For Cu-catalyzed MCRs with sulfonyl azides see: (a) Cassidy, M. P.; Raushel, J.; Fokin, V. V. Angew. Chem., Int. Ed. 2006, 45, 3154-3157.
    • (2006) Angew. Chem., Int. Ed , vol.45 , pp. 3154-3157
    • Cassidy, M.P.1    Raushel, J.2    Fokin, V.V.3
  • 25
    • 34247620302 scopus 로고    scopus 로고
    • Our recently developed method for the synthesis of propargyl glycosides was utilized where possible to make the required sugar alkynes; see: Roy, B, Mukhopadhyay, B. Tetrahedron Lett. 2007, 48, 3783-3787
    • Our recently developed method for the synthesis of propargyl glycosides was utilized where possible to make the required sugar alkynes; see: Roy, B.; Mukhopadhyay, B. Tetrahedron Lett. 2007, 48, 3783-3787.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.