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Volumn 46, Issue 4, 2010, Pages 568-570

Expedient access to branched allylic silanes by copper-catalysed allylic substitution of linear allylic halides

Author keywords

[No Author keywords available]

Indexed keywords

BROMINE DERIVATIVE; CARBON; CHLORIDE; COPPER; HALIDE; SILANE DERIVATIVE; SILICON;

EID: 75149122401     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b920793g     Document Type: Article
Times cited : (51)

References (28)
  • 3
    • 18244375820 scopus 로고    scopus 로고
    • For a recent review on the chemistry of allylic silanes, see:
    • For a recent review on the chemistry of allylic silanes, see: M. Oestreich G. Auer Adv. Synth. Catal. 2005 347 637 640
    • (2005) Adv. Synth. Catal. , vol.347 , pp. 637-640
    • Oestreich, M.1    Auer, G.2
  • 5
    • 0842299374 scopus 로고    scopus 로고
    • ed., I. Fleming and S. V. Ley, Thieme, Stuttgart For the preparation of allylic silanes, see: Hoveyda et al. elaborated an indirect synthesis of branched allylic silanes by copper-catalysed allylic substitution of allylic phosphates using zinc reagents:
    • For the preparation of allylic silanes, see: T. K. Sarkar, in Science of Synthesis, ed., I. Fleming, and, S. V. Ley, Thieme, Stuttgart, 2002, vol. 4, pp. 837-925
    • (2002) Science of Synthesis , pp. 837-925
    • Sarkar, T.K.1
  • 11
    • 0013107235 scopus 로고    scopus 로고
    • ed., N. Krause, Wiley-VCH, Weinheim For a comprehensive summary, see:
    • R. K. Dieter, in Modern Organocopper Chemistry, ed., N. Krause, Wiley-VCH, Weinheim, 2002, pp. 79-144
    • (2002) Modern Organocopper Chemistry , pp. 79-144
    • Dieter, R.K.1
  • 21
    • 0023475212 scopus 로고
    • 2SiCu·LiCN in total synthesis, see:
    • 2SiCu·LiCN in total synthesis, see: E. J. Corey R. M. Burk Tetrahedron Lett. 1987 28 6413 6416
    • (1987) Tetrahedron Lett. , vol.28 , pp. 6413-6416
    • Corey, E.J.1    Burk, R.M.2
  • 25
    • 0037139491 scopus 로고    scopus 로고
    • 2O and benzene were superior to other common polar and non-polar solvents C-C bond formation: palladium-catalysed cross-coupling of vinylic bromides and Grignard reagents:
    • 2O and benzene were superior to other common polar and non-polar solvents C-C bond formation: palladium-catalysed cross-coupling of vinylic bromides and Grignard reagents: B. Radetich E. J. Corey J. Am. Chem. Soc. 2002 124 2430 2431
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 2430-2431
    • Radetich, B.1    Corey, E.J.2
  • 27
    • 35548964277 scopus 로고    scopus 로고
    • C-H bond formation: palladium-catalysed allylic substitution of allylic carbonates with formic acid:
    • C-H bond formation: palladium-catalysed allylic substitution of allylic carbonates with formic acid: S. Hayashi K. Hirano H. Yorimitsu K. Oshima J. Am. Chem. Soc. 2007 129 12650 12651
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 12650-12651
    • Hayashi, S.1    Hirano, K.2    Yorimitsu, H.3    Oshima, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.