Stereoselective synthesis of multi-functionalized chiral silacyclopentanes

Autor: Kuroo, Akihiro, Igawa, Kazunobu, Tomooka, Katsuhiko
Zdroj: Chemistry Letters; March 2024, Vol. 53 Issue: 3
Abstrakt: We have synthesized multifunctionalized silacyclopentanes in a highly selective manner from enantioenriched silacyclopentenol, which is readily accessible from achiral silacyclopentene oxide by enantioselective β-elimination. Functionalization at C2, C4, and C5 positions of silacyclopentenol was achieved based on the regio- and stereoselective nucleophilic substitution reaction of epoxides.We have synthesized multifunctionalized silacyclopentanes in a highly selective manner from enantioenriched silacyclopentenol, which is readily accessible from achiral silacyclopentene oxide by enantioselective β-elimination. Functionalization at C2, C4, and C5 positions of silacyclopentenol was achieved based on the regio- and stereoselective nucleophilic substitution reaction of epoxides.
Databáze: Supplemental Index