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Volumn 17, Issue 3, 2013, Pages 397-405

A robust first-pass protocol for the heck-mizoroki reaction

Author keywords

[No Author keywords available]

Indexed keywords

BOND FORMING; EXPERIMENTAL PROTOCOLS; HECK-MIZOROKI; HECK-MIZOROKI REACTION; STABLE CATALYSTS;

EID: 84875154438     PISSN: 10836160     EISSN: 1520586X     Source Type: Journal    
DOI: 10.1021/op300364p     Document Type: Article
Times cited : (45)

References (60)
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    • Use of electron-rich phosphine ligands -1564
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    • Use of N-heterocyclic carbene ligands -1449
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    • Marion, N.1    Nolan, S.P.2
  • 17
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    • Coupling reactions of aryl chlorides -4211
    • Coupling reactions of aryl chlorides: Littke, A. F.; Fu, G. C. Angew. Chem., Int. Ed. 2002, 41, 4176-4211
    • (2002) Angew. Chem., Int. Ed , vol.41 , pp. 4176
    • Littke, A.F.1    Fu, G.C.2
  • 21
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    • Ligandless anionic intermediates -81
    • Ligandless anionic intermediates: Carrow, B. P.; Hartwig, J. F. J. Am. Chem. Soc. 2010, 132, 79-81
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 79
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    • Transition-Metal-Mediated C-C and C-N Bond Formation
    • For a review of industrial applications of transition metal-catalyzed reactions
    • For a review of industrial applications of transition metal-catalyzed reactions, see: Transition-Metal-Mediated C-C and C-N Bond Formation. Org. Process Res. Dev. 2008, 12, 467-546
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    • For a very recent disclosure of an amination "user's guide" see
    • For a very recent disclosure of an amination "user's guide", see: Surry, D. S.; Buchwald, S. L. Chem. Sci. 2011, 2, 27-50
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    • in the presence of substoichiometric TBAC
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    • Heck reactions of pyridyl substrates often require elevated reaction temperatures or elongated reaction times. See, for instance
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.