- Diastereoselective synthesis of alpha-tocopherol: a new concept for the formation of chromanols.
Diastereoselective synthesis of alpha-tocopherol: a new concept for the formation of chromanols.
Organic letters (2008-10-22)
Julien Chapelat, Axel Buss, Antoinette Chougnet, Wolf-D Woggon
PMID18937482
摘要
A diastereoselective synthesis of alpha-tocopherol 1 (93% de) was achieved via two key steps, (i) a highly diastereoselective Shi epoxidation of a trisubstituted alkene and (ii) an acid supported, "anti-Baldwin" epoxide ring opening under inversion of configuration leading to the 6-membered chromanol ring.
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