Chiral synthesis of lignan lactones, (–)-hinokinin, (–)-deoxypodorhizone, (–)-isohibalactone and (–)-savinin by means of enantioselective deprotonation strategy

Toshio Honda, Nobuaki Kimura, Shigeki Sato, Daishiro Kato, Hideo Tominaga

Journal of the Chemical Society Perkin Transactions 1 · 1994 · 46 citations · 18 references

Concepts

Abstract

Chiral synthesis of lignan lactones, (–)-hinokinin, (–)-deoxypodorhizone, (–)-isohibalactone and (–)-savinin, has been achieved by employing an enantioselective deprotonation of 3-(3,4-methylenedioxybenzyl)cyclobutanone with lithium (S, S′)-α,α′-dimethyldibenzylamide, as a key step.

References

18