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Volumn 31, Issue 11, 2012, Pages 4356-4366

Mechanistic origin of regioselectivity in nickel-catalyzed olefin hydroheteroarylation through C-H activation

Author keywords

[No Author keywords available]

Indexed keywords

1-HEXENE; ALKYL GROUPS; ARYL GROUP; BENZOXAZOLE; C-H ACTIVATION; DENSITY FUNCTIONAL THEORY CALCULATIONS; DIARYLALKANES; ELECTRON-DEFICIENT; EXPERIMENTAL OBSERVATION; HETEROARENES; KEY FACTORS; ORBITAL INTERACTION; ORBITAL OVERLAP; OXIDATIVE ADDITIONS; REDUCTIVE ELIMINATION; STERIC EFFECT; TRANSITION STATE; VINYLARENES;

EID: 84862142762     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om300329z     Document Type: Article
Times cited : (51)

References (73)
  • 73
    • 70350063289 scopus 로고    scopus 로고
    • In addition to the π system of an aryl group or vinyl group, the coordination of the oxygen of an acyl group to metal in the transition state is also expected to facilitate reductive elimination; see: In; Wiley-VCH: Weinheim, Germany
    • In addition to the π system of an aryl group or vinyl group, the coordination of the oxygen of an acyl group to metal in the transition state is also expected to facilitate reductive elimination; see: Hartwig, J. F. In Organotransition Metal Chemistry: From Bonding to Catalysis; Wiley-VCH: Weinheim, Germany, 2010.
    • (2010) Organotransition Metal Chemistry: From Bonding to Catalysis
    • Hartwig, J.F.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.