Issue 0, 1987

Asymmetric conjugate addition to unsaturated chiral amido alcohols using Grignard reagents co-ordinated with tertiary amines or DBU. Preparation of optically active 3-substituted carboxylic acids and (S)-(–)-citronellol

Abstract

Optically active 3-substituted carboxylic acids and (S)-(–)-citronellol have been obtained by diastereoselective conjugate addition of Grignard reagents co-ordinated with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) to chiral amido alcohols derived from (S)-proline.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1987, 1909-1914

Asymmetric conjugate addition to unsaturated chiral amido alcohols using Grignard reagents co-ordinated with tertiary amines or DBU. Preparation of optically active 3-substituted carboxylic acids and (S)-(–)-citronellol

K. Soai, H. Machida and N. Yokota, J. Chem. Soc., Perkin Trans. 1, 1987, 1909 DOI: 10.1039/P19870001909

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