Synthesis of novel coordination compounds of 5-aryl-4,5-dihydro-3-(2-hydroxyphenyl)pyrazoles as potential fungicides

Article abstract of DOI:10.1080/00945719909349480

Base-catalyzed condensation of 2-hydroxyacetophenone with araldehydes gave 3-aryl-1-(2-hydroxyphenyl)prop-2-en-1-ones with E-configuration, which on cyclization with hydrazine hydrate afforded the title ligands, 5-aryl-4,5-dihydro-3-(2-hydroxyphenyl)pyraz

Full text of DOI:10.1080/00945719909349480

This article was downloaded by: [McMaster University]
On: 17 December 2014, At: 08:33
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
Synthesis and Reactivity in
Inorganic and Metal-Organic
Chemistry
Publication details, including instructions for
authors and subscription information:
http://www.tandfonline.com/loi/lsrt19
Synthesis of Novel
Coordination Compounds
of 5-Aryl-4, S-Dihydro-3-(2-
Hydroxyphenyl)Pyrazoles as
Potential Fungicides
Nisha Singh a , Naresh K. Sangwan a & Kuldip Singh
Dhindsa a
a Department of Chemistry & Biochemistry , CCS
Haryana Agricultural University , Hisar, 125 004,
India
Published online: 14 Apr 2008.
To cite this article: Nisha Singh , Naresh K. Sangwan & Kuldip Singh Dhindsa
(1999) Synthesis of Novel Coordination Compounds of 5-Aryl-4, S-Dihydro-3-(2-
Hydroxyphenyl)Pyrazoles as Potential Fungicides, Synthesis and Reactivity in Inorganic
and Metal-Organic Chemistry, 29:4, 673-685, DOI: 10.1080/00945719909349480
To link to this article: http://dx.doi.org/10.1080/00945719909349480
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