Stereoselective Hydrocoupling of Cinnamic Acid Esters by

The electroreduction of Ar-substituted methyl cinnamates in acetonitrile gave all-trans cyclized ... the hydrocoupling of methyl cinnamate to explain ...
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Stereoselective Hydrocoupling of Cinnamic Acid Esters by Electroreduction: Application to Asymmetric Synthesis of Hydrodimers Naoki Kise,* Shumei Iitaka, Keisuke Iwasaki, and Nasuo Ueda Department of Biotechnology, Faculty of Engineering, Tottori University, Koyama, Tottori 680-8552, Japan [email protected] Received July 11, 2002

The electroreduction of Ar-substituted methyl cinnamates in acetonitrile gave all-trans cyclized hydrodimers stereoselectively (58∼90% de). In all cases, small amounts (