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Volumn 78, Issue 19, 2013, Pages 9865-9875

1,5-disubstituted 1,2,3-triazolylation at C1, C2, C3, C4, and C6 of pyranosides: A metal-free route to triazolylated monosaccharides and triazole-linked disaccharides

Author keywords

[No Author keywords available]

Indexed keywords

1 ,3-DIPOLARCYCLOADDITION; ELEVATED TEMPERATURE; METAL CATALYST; PYRANOSIDES; REACTION CONDITIONS; STYRENE EPOXIDE; TERMINAL POSITION; VINYL SULFONES;

EID: 84885168038     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo401576n     Document Type: Article
Times cited : (48)

References (104)
  • 76
    • 81855161831 scopus 로고    scopus 로고
    • Intramolecular azide-alkyne cycloaddition reactions of specially functionalized carbohydrates almost always afforded 1,5-disubstituted triazoles without any metal catalysis; see
    • Intramolecular azide-alkyne cycloaddition reactions of specially functionalized carbohydrates almost always afforded 1,5-disubstituted triazoles without any metal catalysis; see: Majumdar, K. C.; Ray, K. Synthesis 2011, 23, 3767-3783
    • (2011) Synthesis , vol.23 , pp. 3767-3783
    • Majumdar, K.C.1    Ray, K.2
  • 94
  • 104
    • 64549117824 scopus 로고    scopus 로고
    • We observed that the reactions worked well only when both the carbohydrate components were insoluble in water. We therefore presume that these reactions may be categorized as examples of reactions "on water". For a review on this class of reactions, see: Chanda, A.; Fokin, V. V. Chem. Rev. 2009, 109, 725-748
    • (2009) Chem. Rev. , vol.109 , pp. 725-748
    • Chanda, A.1    Fokin, V.V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.