A novel synthesis of thieno[2,3-C]pyrazole

Article abstract of DOI:10.1080/00397919908086238

A new method was found for the synthesis of pyrazoleacetate esters from pyrazolaldehyde. By a new tandem reaction, in which 4-pyrazoleacetate esters reacted with carbon disulfide and iodomethane, thieno[2,3-c]pyrazole was synthesized. This was an easy met

Full text of DOI:10.1080/00397919908086238

This article was downloaded by: [University Of Maryland]
On: 14 October 2014, At: 14:00
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 Novel Synthesis of Thieno[2,3-
C]pyrazole
Zhongwen Wang a , Zhengming Li a , Jun Ren a & Hansong
Chen a
a State Key Laboratry of Elemento-Organic Chemistry,
Institute of Elemento-Organic Chemistry, Nankai University ,
Tianjin, P.R. China , 300071
Published online: 17 Sep 2007.
To cite this article: Zhongwen Wang , Zhengming Li , Jun Ren & Hansong Chen (1999) A
Novel Synthesis of Thieno[2,3-C]pyrazole, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 29:13, 2355-2359, DOI:
10.1080/00397919908086238
To link to this article: http://dx.doi.org/10.1080/00397919908086238
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