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Volumn 54, Issue 10, 2013, Pages 1264-1267

Regio- and stereoselective preparation of (Z)-silyl enol ethers by three-component coupling using α,β-unsaturated acylsilanes as core building blocks

Author keywords

Conjugate addition; Copper(I) tert butoxide; Silyl enol ethers; Silyl migration; Three component coupling

Indexed keywords

ALPHA BETA UNSATURATED ACYSILANE DERIVATIVE; SILANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84873187400     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.12.089     Document Type: Article
Times cited : (16)

References (47)
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    • For copper(I)-mediated conjugate addition of vinyl Grignard reagent to (E)-1-(methyldiphenylsilyl)-3-phenyl-2-propen-1-one, see
    • For copper(I)-mediated conjugate addition of vinyl Grignard reagent to (E)-1-(methyldiphenylsilyl)-3-phenyl-2-propen-1-one, see Y.-M. Tsai, and J.-A. Sieh J. Chin. Chem. Soc. 46 1999 825
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    • Tsai, Y.-M.1    Sieh, J.-A.2
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    • 0000339133 scopus 로고
    • For titanium(IV) chloride-mediated conjugate addition to α,β-unsaturated acylsilanes, see
    • For titanium(IV) chloride-mediated conjugate addition to α,β-unsaturated acylsilanes, see R.L. Danheiser, and D.M. Fink Tetrahedron Lett. 26 1985 2509
    • (1985) Tetrahedron Lett. , vol.26 , pp. 2509
    • Danheiser, R.L.1    Fink, D.M.2
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    • Conjugate dienic silyl enol ethers were preferentially formed when β, γ-unsaturated ketones were deprotonated and then silylated, see
    • Conjugate dienic silyl enol ethers were preferentially formed when β, γ-unsaturated ketones were deprotonated and then silylated, see: A. Devasagayaraj, L. Schwink, and P. Knochel J. Org. Chem. 60 1995 3311
    • (1995) J. Org. Chem. , vol.60 , pp. 3311
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    • Alternatively preferential formation of (E)-enolates of acylsilanes might be rationalized by the presence of a polar aprotic co-solvent, see
    • Alternatively preferential formation of (E)-enolates of acylsilanes might be rationalized by the presence of a polar aprotic co-solvent, see: M. Honda, W. Oguchi, M. Segi, and T. Nakajima Tetrahedron 58 2002 6815
    • (2002) Tetrahedron , vol.58 , pp. 6815
    • Honda, M.1    Oguchi, W.2    Segi, M.3    Nakajima, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.