cheminform abstract: reaction of ynolate anions derived from silylketenes with electrophiles: a...

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1996 organo-silicon compounds, acyclic C derivatives organo-silicon compounds, acyclic C derivatives S 0062 43 - 158 Reaction of Ynolate Anions Derived from Silylketenes with Elec- trophiles: A Facile Preparation of Silyl Ynol Ethers and Functional- ized Silylketenes. The ynolate anions generated from (I) are shown to react with various silyl and stannyl chlorides (II) and (IV) to give either the silyl ynol ethers (III) or the functionalized silylketenes (V) depending on the bulky or small and hard or soft character of the electrophiles. — (AKAI, S.; KITAGAKI, S.; NAKA, T.; YAMAMOTO, K.; TSUZUKI, Y.; MATSUMOTO, K.; KITA, Y.; J. Chem. Soc., Perkin Trans. 1 (1996) 14, 1705-1709; Fac. Pharm. Sci., Osaka Univ., Suita, Osaka 565, Japan; EN) 1

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Page 1: ChemInform Abstract: Reaction of Ynolate Anions Derived from Silylketenes with Electrophiles: A Facile Preparation of Silyl Ynol Ethers and Functionalized Silylketenes

1996 organo-silicon compounds, acyclic C derivatives

organo-silicon compounds, acyclic C derivativesS 0062

43 - 158Reaction of Ynolate Anions Derived from Silylketenes with Elec-trophiles: A Facile Preparation of Silyl Ynol Ethers and Functional-ized Silylketenes. — The ynolate anions generated from (I) are shown toreact with various silyl and stannyl chlorides (II) and (IV) to give either thesilyl ynol ethers (III) or the functionalized silylketenes (V) depending on thebulky or small and hard or soft character of the electrophiles. — (AKAI, S.;KITAGAKI, S.; NAKA, T.; YAMAMOTO, K.; TSUZUKI, Y.; MATSUMOTO,K.; KITA, Y.; J. Chem. Soc., Perkin Trans. 1 (1996) 14, 1705-1709; Fac.Pharm. Sci., Osaka Univ., Suita, Osaka 565, Japan; EN)

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