File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

박철민

Park, Cheol-Min
Synthetic and Medicinal Chemistry Lab.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Catalyst-free electrosynthesis of benzothiophenes from 2-alkenylaryl disulfides

Author(s)
Lee, JuyeongYu, EunsooPark, Cheol-Min
Issued Date
2022-09
DOI
10.1039/d2ob01402e
URI
https://scholarworks.unist.ac.kr/handle/201301/59532
Fulltext
https://pubs.rsc.org/en/content/articlelanding/2022/OB/D2OB01402E
Citation
ORGANIC & BIOMOLECULAR CHEMISTRY, v.20, no.37, pp.7499 - 7502
Abstract
The synthesis of benzothiophenes through electrosynthesis under oxidant- and metal-free conditions has been discovered. Electrolysis of symmetrical 2-alkenylaryl disulfides using an undivided cell leads to the formation of the corresponding benzothiophenes in good to moderate yields with good functional group tolerance. The usefulness of this methodology was further investigated with a scale-up experiment, which delivered a similar result to that of the small scale reaction. Several mechanistic investigations including DFT calculations were carried out to elucidate the reaction mechanism.
Publisher
ROYAL SOC CHEMISTRY
ISSN
1477-0520
Keyword
CLEAVAGETHIOLATIONBONDSMETAL-FREESULFONATED BENZOTHIOPHENESELECTROGENERATED ACID

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.