75000-14-5Relevant academic research and scientific papers
Studies on Heterocyclic Chemistry. Part 24. Syntheses of the 4-Arylisothiazol-3-yl O-Thioesters utilising the S-Thioester --> O-Thioester Rearrangements of the 4-Aryl-5-thioxo-3-isothiazolin-3-yl S-Thioesters induced by Acylation Reagents, Peracid, or N-B
Nishiwaki, Tarozaemon,Kawamura, Etsuko,Abe, Noritaka,Iori, Mistuo
, p. 1401 - 1406 (2007/10/02)
A number of 4-arylisothiazol-3-yl O-thioesters have been prepared utilising the S-thioester -> O-thioester rearrangements of the 4-aryl-5-thioxo-3-isothiazolin-3-yl S-thioesters (1).Reactions of the isothiazolines with acylation reagents (e.g. acyl chlori
THIOL-ESTER-THIONO-ESTER REARRANGEMENTS INDUCED BY ALKYLATING REAGENTS, PERACIDS, OR N-HALOSUCCINIMIDE IN THE 3-ACYLTHIO-4-ARYL-3-ISOTHIAZOLINE-5-THIONE SYSTEM
Nishiwaki, Tarozaemon,Kawamura, Etsuko,Abe, Noritaka,Iori, Mitsuo
, p. 401 - 402 (2007/10/02)
Alkylations of 3-acylthio-4-aryl-3-isothiazoline-5-thiones with diazomethane, triethyloxonium tetrafluoroborate, or alkyl iodide afford 5-alkylthio-4-aryl-3-thioacyloxyisothiazoles, whereas the reactions of these isothiazolines with peracids or N-halosucc
