Chemical and Pharmaceutical Bulletin, Год журнала: 2024, Номер 72(11), С. 1034 - 1037

Опубликована: Ноя. 29, 2024

This study introduces a novel method for ring-closing chlorosulfenylation of alkenoic thioesters using N-chlorosuccinimide in hexafluoroisopropanol under mild conditions. reaction efficiently forms five-membered cyclic sulfur compounds with high selectivity, representing significant advancement the synthesis chlorinated S-heterocycles. Computational analysis density functional theory demonstrates superiority thioester nucleophiles over traditional benzyl sulfides this reaction, highlighting energetic preference thioesters.

Язык: Английский