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ChemInform Abstract: Silicon‐Functionalized Silyl Enol Ethers: A Novel Dialkylchlorosilyl Enol Ether and Its Conversion to Alkoxy and Aminosilyl Enol Ethers.

Robert D. Walkup

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Abstract

Abstract The lithium enolate (II) derived from pinacolone (I) is converted to the chlorosilyl enol ether (III) which undergoes substitution reactions with the nucleophiles (IV), yielding the alkoxy or aminosilyl enol ethers (V).

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What this paper is about

Abstract The lithium enolate (II) derived from pinacolone (I) is converted to the chlorosilyl enol ether (III) which undergoes substitution reactions with the nucleophiles (IV), yielding the alkoxy or aminosilyl enol ethers (V).

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Available abstract

Abstract The lithium enolate (II) derived from pinacolone (I) is converted to the chlorosilyl enol ether (III) which undergoes substitution reactions with the nucleophiles (IV), yielding the alkoxy or aminosilyl enol ethers (V).

Key concepts: Chemistry, Enol, Enol ether, Alkoxy group, Silylation, Silyl enol ether, Ether, Lithium (medication)

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ChemInform Abstract: Silicon‐Functionalized Silyl Enol Ethers: A Novel Dialkylchlorosilyl Enol Ether and Its Conversion to Alkoxy and Aminosilyl Enol Ethers. — Research Paper | ScholarLens