Enantioselective total syntheses of six natural and two proposed meroterpenoids from Psoralea corylifolia

The first enantioselective total syntheses of six natural and two proposed meroterpenoids isolated from Psoralea corylifolia have been achieved in 7-9 steps from 2-methylcyclohexanone. The current synthetic approaches feature a high level of synthetic flexibility, stereodivergent fashion and short synthetic route, thereby providing a potential platform for the preparation of numerous this-type meroterpenoids and their pseudo-natural products.

Automated summary

The first enantioselective total syntheses of six natural and two proposed meroterpenoids from Psoralea corylifolia have been achieved in 7-9 steps from 2-methylcyclohexanone. These synthetic approaches offer a high level of flexibility, stereodivergent fashion, and short route, providing a potential platform for the preparation of various this-type meroterpenoids and their pseudo-natural products.