Issue 16, 1984

Highly diastereofacial selective addition of nucleophiles to 2-alkyl-3-trimethylsilyl alk-3-enyl carbonyl compounds. Stereoselective preparation of β-methylhomoallyl alcohols and β-hydroxy-α-methyl ketones

Abstract

Nucleophiles react with 2-alkyl-3-trimethylsilylalk-3-enyl carbonyl compounds to afford ‘Cram’ products with high diastereoselectivity; this allows the stereoselective preparation of β-methylhomoally alcohols and β-hydroxy-α-methyl ketones.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 1130-1132

Highly diastereofacial selective addition of nucleophiles to 2-alkyl-3-trimethylsilyl alk-3-enyl carbonyl compounds. Stereoselective preparation of β-methylhomoallyl alcohols and β-hydroxy-α-methyl ketones

F. Sato, M. Kusakabe and Y. Kobayashi, J. Chem. Soc., Chem. Commun., 1984, 1130 DOI: 10.1039/C39840001130

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