메뉴 건너뛰기




Volumn 32, Issue 24, 2013, Pages 7424-7430

Activation of C-F and Ni-C bonds of [P,S]-ligated nickel perfluorometallacycles

Author keywords

[No Author keywords available]

Indexed keywords

ORGANOMETALLICS; SYNTHESIS (CHEMICAL);

EID: 84896529019     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om400933k     Document Type: Article
Times cited : (26)

References (57)
  • 17
    • 0005173866 scopus 로고
    • Stone reported reactivity studies of a related tetracarbonyl iron perfluorocyclopentane complex. The product decomposed with heating at 70 C for 120 h, affording perfluorocyclobutane as the major organic product. With heating at 160 C for 12 days, perfluorocyclobutene was obtained as the major organic product
    • Stone reported reactivity studies of a related tetracarbonyl iron perfluorocyclopentane complex. The product decomposed with heating at 70 C for 120 h, affording perfluorocyclobutane as the major organic product. With heating at 160 C for 12 days, perfluorocyclobutene was obtained as the major organic product: Manuel, T. A.; Stafford, S. L.; Stone, F. G. A. J. Am. Chem. Soc. 1961, 83, 249
    • (1961) J. Am. Chem. Soc. , vol.83 , pp. 249
    • Manuel, T.A.1    Stafford, S.L.2    Stone, F.G.A.3
  • 19
    • 84896538304 scopus 로고    scopus 로고
    • (E. I. Du Pont de Nemours & Co.) PCT Int. Appl. U.S. Patent 5,670,679, The preparation of unsaturated hydrofluorocarbons (HFCs) is an attractive target, as several such molecules have been shown to have drastically reduced global warming potential (vs saturated HFCs)
    • Baker, R. T.; Beatty, R. P.; Farnham, W. B.; Wallace, R. L., Jr. (E. I. Du Pont de Nemours & Co.) PCT Int. Appl. U.S. Patent 5,670,679, 1997. The preparation of unsaturated hydrofluorocarbons (HFCs) is an attractive target, as several such molecules have been shown to have drastically reduced global warming potential (vs saturated HFCs): http://www.unep.org/dewa/portals/67/pdf/ HFC-report.pdf.
    • (1997)
    • Baker, R.T.1    Beatty, R.P.2    Farnham, W.B.3    Wallace, Jr.R.L.4
  • 42
    • 84896525279 scopus 로고    scopus 로고
    • Synthesis and Use of Chiral Sulfur Ylides
    • In; Wiley-VCH: Weinheim, Germany, pp and references therein. - 208
    • Toru, T.; Bolm, C.; Brière, J.-F.; Metzner, P. Synthesis and Use of Chiral Sulfur Ylides. In Organosulfur Chemistry in Asymmetric Synthesis; Wiley-VCH: Weinheim, Germany, 2008; pp 179-208 and references therein.
    • (2008) Organosulfur Chemistry in Asymmetric Synthesis , pp. 179
    • Toru, T.1    Bolm, C.2    Brière, J.-F.3    Metzner, P.4
  • 55
    • 84896512743 scopus 로고    scopus 로고
    • (E. I. Du Pont de Nemours & Co.) U. S. Pat. Appl. Publ. U.S. Patent 2006106263
    • Miller, R. N.; Nappa, M. J.; Rao, V. N. M.; Sievert, A. C. (E. I. Du Pont de Nemours & Co.) U. S. Pat. Appl. Publ., U.S. Patent 2006106263, 2006.
    • (2006)
    • Miller, R.N.1    Nappa, M.J.2    Rao, V.N.M.3    Sievert, A.C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.