메뉴 건너뛰기




Volumn 34, Issue 4, 2015, Pages 790-799

Direct and transfer hydrosilylation reactions catalyzed by fully or partially fluorinated triarylboranes: A systematic study

Author keywords

[No Author keywords available]

Indexed keywords

ATOMS; BORON; HYDROSILYLATION; KETONES; SILANES; SILICON;

EID: 84923360593     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om501284a     Document Type: Article
Times cited : (81)

References (62)
  • 9
    • 84877307150 scopus 로고    scopus 로고
    • For a comprehensive list of synthetic applications, see: and references therein
    • For a comprehensive list of synthetic applications, see: Robert, T.; Oestreich, M. Angew. Chem., Int. Ed. 2013, 52, 5216-5218 and references therein
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 5216-5218
    • Robert, T.1    Oestreich, M.2
  • 13
    • 84884686351 scopus 로고    scopus 로고
    • Eds. Topics in Current Chemistry 334; Springer: Heidelberg, Germany, For a review, see
    • Frustrated Lewis Pairs II, Expanding the Scope; Erker, G.; Stephan, D. W., Eds.; Topics in Current Chemistry 334; Springer: Heidelberg, Germany, 2013. For a review, see
    • (2013) Frustrated Lewis Pairs II, Expanding the Scope
    • Erker, G.1    Stephan, D.W.2
  • 32
    • 84919741139 scopus 로고    scopus 로고
    • 3-catalyzed preparation of benzannulated siloles during the preparation of this manuscript
    • 3-catalyzed preparation of benzannulated siloles during the preparation of this manuscript. Curless, L. D.; Ingleson, M. J. Organometallics 2014, 33, 7241-7246
    • (2014) Organometallics , vol.33 , pp. 7241-7246
    • Curless, L.D.1    Ingleson, M.J.2
  • 34
    • 14644434745 scopus 로고    scopus 로고
    • For the first example of the Piers-Rubinsztajn reaction, see
    • For the first example of the Piers-Rubinsztajn reaction, see: Rubinsztajn, S.; Cella, J. A. Polym. Prepr. 2004, 45, 635-636
    • (2004) Polym. Prepr. , vol.45 , pp. 635-636
    • Rubinsztajn, S.1    Cella, J.A.2
  • 46
    • 80051500596 scopus 로고    scopus 로고
    • For theoretical studies of Lewis acidities of tris(fluorophenyl)-substituted boranes, see
    • For theoretical studies of Lewis acidities of tris(fluorophenyl)-substituted boranes, see: Durfey, B. L.; Gilbert, T. M. Inorg. Chem. 2011, 50, 7871-7879
    • (2011) Inorg. Chem. , vol.50 , pp. 7871-7879
    • Durfey, B.L.1    Gilbert, T.M.2
  • 58
    • 84923365835 scopus 로고    scopus 로고
    • The double-bond geometry was determined by an X-ray diffraction analysis, but its quality prevents its publication. The CIF file was deposited with the Cambridge Structural Database as a personal communication (Sebastian Keess, CCDC-1039000)
    • The double-bond geometry was determined by an X-ray diffraction analysis, but its quality prevents its publication. The CIF file was deposited with the Cambridge Structural Database as a personal communication (Sebastian Keess, 2014, CCDC-1039000).
    • (2014)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.