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Synfacts 2010(11): 1303-1303
DOI: 10.1055/s-0030-1258781
DOI: 10.1055/s-0030-1258781
Organo- and Biocatalysis
© Georg Thieme Verlag
Stuttgart ˙ New York
Entropy-Controlled Asymmetric Catalysis
Y. Sohtome*, B. Shin, N. Horitsugi, R. Takagi, K. Noguchi, K. Nagasawa*
Tokyo University of Agriculture and Technology, Japan
Further Information
Publication History
Publication Date:
21 October 2010 (online)
Significance
Sohtome, Nagasawa, and colleagues report an enantioselective Friedel-Crafts reaction of phenols and nitroolefins using their recently developed flexible guanidine/bisthiourea catalyst 3. Extensive catalyst development allowed the authors to achieve very good enantio- and chemoselectivity in the reaction, which is normally prone to cascade processes. Kinetic studies based on the Eyring equation revealed an unprecedented mode of enantiodifferentiation based solely on entropic control. This type of activation is equally efficient over a wide range of temperatures and the entropy term can be presumably tuned by changing the reaction conditions.