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Volumn 24, Issue 20, 2013, Pages 2723-2729

An investigation of the asymmetric Huisgen 'click' reaction 1

Author keywords

asymmetric synthesis; chiral ligands; copper; CuAAC reaction

Indexed keywords

ALKYNE DERIVATIVE; AZIDE; COPPER; METHYL 2 [(1 BENZYL 1H 1,2,3 TRIAZOL 4 YL)METHYL] 2 CYANOPENT 4 YNOATE; TRIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84889878360     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0033-1340152     Document Type: Article
Times cited : (24)

References (45)
  • 2
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    • Recent Advances in Catalytic Asymmetric Desymmetrization Reactions In Mikami K. Lautens M. John Wiley & Sons Hoboken
    • Rovis T. Recent Advances in Catalytic Asymmetric Desymmetrization Reactions In New Frontiers in Asymmetric Catalysis. Mikami K., Lautens M. John Wiley & Sons Hoboken: 2007; 275 311
    • (2007) New Frontiers in Asymmetric Catalysis , pp. 275-311
    • Rovis, T.1
  • 9
    • 0003735580 scopus 로고    scopus 로고
    • Asymmetric Palladium-Catalysed Coupling Reactions In Stephenson G.R. Kluwer Academic Publishers London
    • Stephenson G. R. Asymmetric Palladium-Catalysed Coupling Reactions In Advanced Asymmetric Synthesis. Stephenson G. R. Kluwer Academic Publishers London: 1996; 275 298
    • (1996) Advanced Asymmetric Synthesis , pp. 275-298
    • Stephenson, G.R.1
  • 12
    • 0042288850 scopus 로고    scopus 로고
    • See also: Asymmetric Conjugate Addition Reactions In Stephenson G.R. Kluwer Academic Publishers London
    • See also: Perlmutter P. Asymmetric Conjugate Addition Reactions In Advanced Asymmetric Synthesis. Stephenson G. R. Kluwer Academic Publishers London: 1996; 222 230
    • (1996) Advanced Asymmetric Synthesis , pp. 222-230
    • Perlmutter, P.1
  • 23
    • 0002218143 scopus 로고
    • For the cycloaddition reaction between phenyl azide and an acetylenic ester, see
    • For the cycloaddition reaction between phenyl azide and an acetylenic ester, see: Michael A. J. Prakt. Chem.: 1893; 48 94
    • (1893) J. Prakt. Chem. , vol.48 , pp. 94
    • Michael, A.1
  • 41
    • 77149170018 scopus 로고    scopus 로고
    • For an example of the formation of a bis-triazole from a glycine-derived meso bis-alkyne, see
    • For an example of the formation of a bis-triazole from a glycine-derived meso bis-alkyne, see: Struthers H., Mindt T. L., Schibli R. Dalton Trans.: 2010; 39 675
    • (2010) Dalton Trans. , vol.39 , pp. 675
    • Struthers, H.1    Mindt, T.L.2    Schibli, R.3
  • 42
    • 17644414186 scopus 로고    scopus 로고
    • Statistical mixtures of mono- and bis-triazoles have been reported previously for a 'click' reaction of a meso -diyne performed in the absence of a chiral ligand, see
    • Statistical mixtures of mono- and bis-triazoles have been reported previously for a 'click' reaction of a meso -diyne performed in the absence of a chiral ligand, see: Rodionov V. O., Fokin V. V., Finn M. G. Angew. Chem. Int. Ed.: 2005; 44 2210
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 2210
    • Rodionov, V.O.1    Fokin, V.V.2    Finn, M.G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.