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Volumn 12, Issue 20, 2010, Pages 4556-4559

Mechanistic insights into nickel-catalyzed cycloisomerizations

Author keywords

[No Author keywords available]

Indexed keywords


EID: 77957833792     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101852w     Document Type: Article
Times cited : (15)

References (35)
  • 12
    • 77957842493 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see
  • 23
    • 77957829584 scopus 로고    scopus 로고
    • For related reductive cyclizations of simple enynes, see
    • For related reductive cyclizations of simple enynes, see
  • 30
    • 77957830952 scopus 로고    scopus 로고
    • For leading references to hydrovinylation processes
    • For leading references to hydrovinylation processes
  • 33
    • 77957830602 scopus 로고    scopus 로고
    • A recent report from Louie illustrates that nickel hydride-mediated cycloisomerizations may involve ortho -metallation of an NHC ligand. As our work involves phosphine complexes, nickel hydride generation by this mechanism is unlikely in the present manuscript.
    • A recent report from Louie illustrates that nickel hydride-mediated cycloisomerizations may involve ortho -metallation of an NHC ligand. As our work involves phosphine complexes, nickel hydride generation by this mechanism is unlikely in the present manuscript.
  • 35
    • 77957826001 scopus 로고    scopus 로고
    • The absolute configuration of the enantioenriched ketone was not determined.
    • The absolute configuration of the enantioenriched ketone was not determined.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.