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Volumn , Issue 1, 2008, Pages 141-148

Study of copper(I) catalysts for the synthesis of carbanucleosides via azide-alkyne 1,3-dipolar cycloaddition

Author keywords

Carbanucleosides; Copper(I) catalysts; Huisgen 1,3 dipolar cycloaddition; N heterocyclic carbenes

Indexed keywords

CARBANUCLEOSIDES; HUISGEN 1,3-DIPOLAR CYCLOADDITION; N-HETEROCYCLIC CARBENES;

EID: 38349164488     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-990943     Document Type: Article
Times cited : (79)

References (65)
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    • For the copper-catalyzed coupling of terminal alkynes (i.e., the Glaser reaction), see: (a) Glaser, C. Ber. Dtsch. Chem Ges. 1869, 2, 422.
    • For the copper-catalyzed coupling of terminal alkynes (i.e., the Glaser reaction), see: (a) Glaser, C. Ber. Dtsch. Chem Ges. 1869, 2, 422.
  • 38
    • 36849065859 scopus 로고    scopus 로고
    • For recent reviews on NHC ligands, see: a, Nolan, S. P, Ed, Wiley-VCH: Weinheim
    • For recent reviews on NHC ligands, see: (a) N-Heterocyclic Carbenes in Synthesis; Nolan, S. P., Ed.; Wiley-VCH: Weinheim, 2006.
    • (2006) N-Heterocyclic Carbenes in Synthesis
  • 47
    • 38349091303 scopus 로고    scopus 로고
    • CuBr. These data can be obtained free of charge from The Cambridge Crystallographic Data center via
    • File CCDC 654537 contains the complete crystallographic data for (IMes)CuBr. These data can be obtained free of charge from The Cambridge Crystallographic Data center via www.ccdc.cam.ac.uk/data-request/cif.
    • File CCDC 654537 contains the complete crystallographic data for (IMes)
  • 49
    • 33748291815 scopus 로고    scopus 로고
    • Goj, L. A.; Blue, E. D.; Delp, S. A.; Gunnoe, T. B.; Cundari, T. R.; Petersen, J. L. Organometallics 2006, 25, 4097; see also ref. 20a and 23.
    • (b) Goj, L. A.; Blue, E. D.; Delp, S. A.; Gunnoe, T. B.; Cundari, T. R.; Petersen, J. L. Organometallics 2006, 25, 4097; see also ref. 20a and 23.
  • 52
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    • For reviews on microwave-assisted reactions see: a
    • For reviews on microwave-assisted reactions see: (a) Caddick, S. Tetrahedron 1995, 51, 10403.
    • (1995) Tetrahedron , vol.51 , pp. 10403
    • Caddick, S.1
  • 54
    • 0011932271 scopus 로고    scopus 로고
    • Loupy, A, Ed, Wiley-VCH: Weinheim
    • (c) Microwaves in Organic Synthesis; Loupy, A., Ed.; Wiley-VCH: Weinheim, 2002.
    • (2002) Microwaves in Organic Synthesis
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    • Nolte, C.; Mayer, P.; Straub, B. F. Angew. Chem. Int. Ed. 2007, 46, 2001; see also ref. 10.
    • (b) Nolte, C.; Mayer, P.; Straub, B. F. Angew. Chem. Int. Ed. 2007, 46, 2001; see also ref. 10.
  • 62
    • 38349096641 scopus 로고    scopus 로고
    • Ratio 1,4-triazole/1,5-triazole, 65:35
    • Ratio 1,4-triazole/1,5-triazole = 65:35.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.