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
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
[isPartOf]
[URI]http://www.csj.jp/journals/chem-lett/index.html
Schools
大学院医学系研究科（理学）