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Volumn 12, Issue 21, 2010, Pages 4936-4939

One-pot three-step synthesis of 1,2,3-triazoles by copper-catalyzed cycloaddition of azides with alkynes formed by a Sonogashira cross-coupling and desilylation

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNE; AZIDE; COPPER; SILANE DERIVATIVE; TRIAZOLE DERIVATIVE;

EID: 78049492294     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol1022036     Document Type: Article
Times cited : (86)

References (40)
  • 1
    • 78049518645 scopus 로고    scopus 로고
    • For the original publications, see
    • For the original publications, see
  • 26
    • 78049487559 scopus 로고    scopus 로고
    • Heating under microwave irradiation trimethyl(phenylethynyl)silane (1a) with benzyl azide (2a) in the presence of TBAF (1 equiv) at 120 °C for 20 min resulted in less than 5% yield of the corresponding triazole in a 1:1 mixture of regioisomers
    • Heating under microwave irradiation trimethyl(phenylethynyl)silane (1a) with benzyl azide (2a) in the presence of TBAF (1 equiv) at 120 °C for 20 min resulted in less than 5% yield of the corresponding triazole in a 1:1 mixture of regioisomers.
  • 27
    • 78049513063 scopus 로고    scopus 로고
    • 2 catalyzes the cycloaddition
    • 2 catalyzes the cycloaddition.
  • 35
    • 78049522328 scopus 로고    scopus 로고
    • Synthesis of 1-substituted 4-acyl-1 H -1,2,3-triazoles using CuAAC exhibits moderate yield (< 60%). See
    • Synthesis of 1-substituted 4-acyl-1 H -1,2,3-triazoles using CuAAC exhibits moderate yield (< 60%). See


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.