Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000131.xml
Synfacts 2006(10): 1063-1063
DOI: 10.1055/s-2006-949370
DOI: 10.1055/s-2006-949370
Organo- and Biocatalysis
© Georg Thieme Verlag Stuttgart · New York
Enantioselective Aqueous Direct Cross-Aldol Reaction of Aldehydes
S. Aratake, T. Okano, J. Takahashi, T. Sumiya, M. Shoji, Y. Hayashi*
Tokyo University of Science, Japan
Further Information
Publication History
Publication Date:
21 September 2006 (online)
Significance
Here the authors report an asymmetric direct cross-aldol reaction of two different aldehydes in the presence of water without using any additive. While proline itself is not efficient for this reaction, proline-derived catalyst 1 has been found to be effective. With 10 mol% of catalyst 1 moderate to good yields (29-92%) and high enantioselectivities (er = 87:13 to >99:1) are obtained for different acceptor and donor (typically propanaldehyde) aldehydes.