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Volumn 15, Issue 16, 2013, Pages 4066-4069

Mechanism of catalytic functionalization of primary C-H bonds using a silylation strategy

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EID: 84882759279     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol401597t     Document Type: Article
Times cited : (30)

References (34)
  • 26
    • 77952819729 scopus 로고    scopus 로고
    • All computations were performed using the Gaussian09 suite of quantum chemical programs. Frisch, M. J. Gaussian09, rev. A.02; Gaussian Inc.: Wallingford, CT, 2009. See the Supporting Information (SI) for complete list of citations as well as full description of the computational methods.
    • (2009) Gaussian09
    • Frisch, M.J.1
  • 30
    • 84882741796 scopus 로고    scopus 로고
    • 4Me) and [IrH(nbe)(phen)]. The process exhibits a high exoergicity of-32.5 kcal/mol. More details are provided in Figure S1 in the SI.
    • 4Me) and [IrH(nbe)(phen)]. The process exhibits a high exoergicity of-32.5 kcal/mol. More details are provided in Figure S1 in the SI.
  • 31
    • 84856728404 scopus 로고    scopus 로고
    • A similar role of the norbornenyl group was previously suggested in an Ir-catalyzed dehydrogenative cyclization leading to benzosiloles. See: Kuznetsov, A.; Gevorgyan, V. Org. Lett. 2012, 14, 914
    • (2012) Org. Lett. , vol.14 , pp. 914
    • Kuznetsov, A.1    Gevorgyan, V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.