A general and efficient synthesis of 2-phenylbenzothiazoles from diphenyl disulfides

Article abstract of DOI:10.1080/00397919308009825

Benzothiazoles containing a substituted-phenyl at the 2 position can be synthesized cleanly and efficiently from the corresponding bis(2-aminophenyl) disulfide. Bis(2-aminophenyl) disulfides represent a stable source of 2-aminobenzenethiols.

Full text of DOI:10.1080/00397919308009825

This article was downloaded by: [Wilfrid Laurier University]
On: 11 September 2013, At: 07:40
Publisher: Taylor & Francis
Informa Ltd Registered in England and Wales Registered Number: 1072954
Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH,
UK
Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
Publication details, including instructions for
authors and subscription information:
http://www.tandfonline.com/loi/lsyc20
A General and Efficient
Synthesis of 2-
Phenylbenzothiazoles From
Diphenyl Disulfides
Yi-Hua Chang a , John D. Peak a , Scott W. Wierschke
a & William A. Feld a
a Department of Chemistry, Wright State University
Dayton, OH 45435
Published online: 27 Oct 2006.
To cite this article: Yi-Hua Chang , John D. Peak , Scott W. Wierschke & William
A. Feld (1993) A General and Efficient Synthesis of 2-Phenylbenzothiazoles
From Diphenyl Disulfides, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 23:5, 663-670, DOI:
10.1080/00397919308009825
To link to this article: http://dx.doi.org/10.1080/00397919308009825
PLEASE SCROLL DOWN FOR ARTICLE
Taylor & Francis makes every effort to ensure the accuracy of all the
information (the “Content”) contained in the publications on our platform.
However, Taylor & Francis, our agents, and our licensors make no
representations or warranties whatsoever as to the accuracy, completeness,
or suitability for any purpose of the Content. Any opinions and views
expressed in this publication are the opinions and views of the authors, and
are not the views of or endorsed by Taylor & Francis. The accuracy of the
Content should not be relied upon and should be independently verified with
primary sources of information. Taylor and Francis shall not be liable for any

losses, actions, claims, proceedings, demands, costs, expenses, damages,
and other liabilities whatsoever or howsoever caused arising directly or
indirectly in connection with, in relation to or arising out of the use of the
Content.
This article may be used for research, teaching, and private study purposes.
Any substantial or systematic reproduction, redistribution, reselling, loan,
sub-licensing, systematic supply, or distribution in any form to anyone is
expressly forbidden. Terms & Conditions of access and use can be found at
http://www.tandfonline.com/page/terms-and-conditions