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[摘要]:A new synthetic strategy of (S)-()-stepholidine, a promising antipsychotic drug candidate, is described. Nucleophilic addition of a laterally lithiated nitrile to a (5)-tert-butanesulfinylimine was used as the key step, which was complished in 94 % de and the main isomer was isolated in 52% yield. (S)-(-)-St epholidine was prepared after another 5 steps, with an overall yield of 18.3% and > 98% ee. |
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