Reactions with hydrazonoyl halides XXIV[1]: Synthesis of some new unsymmetrical azines and dihydro-1,3,4-thiadiazoles

Article abstract of DOI:10.1080/10426509908031623

Unsymmetrical azines were synthesized from reaction of C-coumarinoyl-N-arylformohydrazonoyl bromide with different alkyl carbodithioates. In addition, reactions of hydrazonoyl halides with thioanilide and methyl dithioates were studied. The structures of newly synthesized compounds were confirmed by elemental analyses, spectroscopic tools, and alternative syntheses whenever possible.

Full text of DOI:10.1080/10426509908031623

This article was downloaded by: [Gazi University]
On: 30 December 2014, At: 22:35
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
Phosphorus, Sulfur, and Silicon
and the Related Elements
Publication details, including instructions for
authors and subscription information:
http://www.tandfonline.com/loi/gpss20
REACTIONS WITH
HYDRAZONOYL HALIDES
XXIV[1]: SYNTHESIS OF
SOME NEW UNSYMMETRICAL
AZINES AND DIHYDRO-1,3,4-
THIADIAZOLES
Abdou O. Abdelhamid a & Gaber S. Mohamed a
a Department of Chemistry, Faculty of Science ,
Cairo University , Giza, Egypt
Published online: 24 Sep 2006.
To cite this article: Abdou O. Abdelhamid & Gaber S. Mohamed (1999) REACTIONS
WITH HYDRAZONOYL HALIDES XXIV[1]: SYNTHESIS OF SOME NEW UNSYMMETRICAL
AZINES AND DIHYDRO-1,3,4-THIADIAZOLES, Phosphorus, Sulfur, and Silicon and the
Related Elements, 152:1, 115-128, DOI: 10.1080/10426509908031623
To link to this article: http://dx.doi.org/10.1080/10426509908031623
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