Issue 12, 1989

Double asymmetric hydrogenation of conjugated dienes catalysed by ruthenium binap complexes

Abstract

Buta-1,3-diene-2,3-dicarboxylic acid is smoothly hydrogenated in the presence of a ruthenium–(R)-binap complex as a catalyst via two consecutive 1,2-hydrogen additions, giving rise to (S,S)-2,3-dimethylsuccinic acid with 98% diastereoisomeric excess and 96% enantiomeric excess.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 769-770

Double asymmetric hydrogenation of conjugated dienes catalysed by ruthenium binap complexes

H. Muramatsu, H. Kawano, Y. Ishii, M. Saburi and Y. Uchida, J. Chem. Soc., Chem. Commun., 1989, 769 DOI: 10.1039/C39890000769

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