THIOL-ESTER-THIONO-ESTER REARRANGEMENTS INDUCED BY ALKYLATING REAGENTS, PERACIDS, OR N-HALOSUCCINIMIDE IN THE 3-ACYLTHIO-4-ARYL-3-ISOTHIAZOLINE-5-THIONE SYSTEM

DOI: 10.1246/cl.1980.401

Source and publish data:

Chemistry Letters p. 401 - 402 (1980)

Update date:2022-08-05

Topics:

Authors:

Nishiwaki, Tarozaemon

Kawamura, Etsuko

Abe, Noritaka

Iori, Mitsuo

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Article abstract of DOI:10.1246/cl.1980.401

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

Full text of DOI:10.1246/cl.1980.401

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