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Enantioselective total synthesis of (-)-(S)-stepholidine, a drug candidate for the treatment of schizophrenia and/or drug abuse, is described. Asymmetric transfer hydrogenation of imines with use of Noyori's catalyst was used as the key step and (-)-(S)-stepholidine was synthesized in 6 steps, with 42% overall yield and >99% ee.

Citation

Jian-Jun Cheng, Yu-She Yang. Enantioselective total synthesis of (-)-(S)-stepholidine. The Journal of organic chemistry. 2009 Dec 4;74(23):9225-8

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PMID: 19950885

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