Abe Noritaka

Affiliate Master Yamaguchi University

Thiol-ester-thiono-ester rearrangements induced by alkylating reagents, peracids, or n-halosuccinimide in the 3-acylthio-4-aryl-3-isothiazoline-5-thione system

Chemistry letters Volume 9 Issue 4 Page 401-402

published_at 1980

Title

Thiol-ester-thiono-ester rearrangements induced by alkylating reagents, peracids, or n-halosuccinimide in the 3-acylthio-4-aryl-3-isothiazoline-5-thione system

Creators Nishiwaki Tarozaemon

Creators Kawamura Etsuko

Creators Abe Noritaka

Creators Iori Mitsuo

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-halosuccinimide produce bis(4-aryl-3-thioacyloxyisothiazol-5-yl) disulfides.

Languages eng

Resource Type journal article

Publishers 日本化学会

Date Issued 1980

File Version Not Applicable (or Unknown)

Access Rights metadata only access

Relations

[ISSN]0366-7022

[NCID]AA00603318

https://doi.org/10.1246/cl.1980.401

[isPartOf] [URI]http://www.csj.jp/journals/chem-lett/index.html

Schools 大学院医学系研究科（理学）