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Enantioselective reduction of cyclopropenyl esters and ketones to optically active cyclopropanes has been achieved by using whole-cell-overexpressing ene-reductases (EREDs). By using these enzymes, trans-cyclopropanes were isolated in good yield and high enantiomeric excess. A wide range of optically active cyclopropane esters and ketones were obtained, and a variety of substituent patterns on the cyclopropenes were tolerated.
Yasukawa et al. (Mon,) studied this question.