The synthesis of some N-[4-substituted phenyl]-3-acetoxybenzthioamides and their N1,N3-disubstituted amidrazones

Article abstract of DOI:10.1080/00397919608003615

The synthesis of N-[4-substituted phenyl]-3-acetoxythiobenzamides 5 from corresponding carboxyamides 4 is described. The reaction of 5 with hydrazine hydrate gave N¹,N³-disubstituted amidrazones. They were characterized by their N

Full text of DOI:10.1080/00397919608003615

This article was downloaded by: [Tulane University]
On: 31 January 2015, At: 08:31
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
The Synthesis of Some N-
[4-Substituted Phenyl]-3-
acetoxybenzthioamides and
Their N 1, N 3 -Disubstituted
Amidrazones
Liljana Jovevska a , Froska Anastasova a &
a
Vasilka Aleksić
a Institute of Chemistry, Faculty of Natural
Sciences and Mathematics St. Cyril and
Methodius University , 91000 Skopje, P. O. Box
162, Republic of Macedonia
Published online: 21 Aug 2006.
To cite this article: Liljana Jovevska , Froska Anastasova & Vasilka Aleksić
(1996) The Synthesis of Some N-[4-Substituted Phenyl]-3-acetoxybenzthioamides
and Their N 1, N 3 -Disubstituted Amidrazones, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry,
26:2, 279-286, DOI: 10.1080/00397919608003615
To link to this article: http://dx.doi.org/10.1080/00397919608003615
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