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Alkylthialactonization: A novel protocol for access to either diastereoisomer of α-(thiomethyl)-γ-butyrolactones
DanielR.Nicponski,P.VeeraraghavanRamachandran
Tetrahedron Letters Pub Date : 06/09/2023 00:00:00 , DOI:10.1016/j.tetlet.2023.154605
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.
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