Alkylthialactonization: A novel protocol for access to either diastereoisomer of α-(thiomethyl)-γ-butyrolactones
DanielR.Nicponski,P.VeeraraghavanRamachandran
Abstract
Presented herein are the first highly diastereoselective, controlled alkylthia-Michael reactions of mercaptans onto α-methylene butanoates. This addition occurs with concomitant lactonization and provides ready access to either the kinetic cis,cis- or thermodynamic cis,trans-butyrolactones under catalytic promotion by tetrabutylammonium hydroxide in methanol.