1,3-Dipolar cycloaddition reactions of C-(2-nitro)-styryl-N-phenyl nitrone leading to the regiospecific and stereospecific synthesis of new isoxazolidine derivatives

Article abstract of DOI:10.1080/00397919608003767

New substituted isoxazolidine derivatives have been synthesized through regiospecific and stereospecific 1,3-dipolar cycloadditions of C-(2-nitro)-styryl-N-phenyl nitrone with reactive dipolarophiles in excellent yields and effects of substituents have been noted.

Full text of DOI:10.1080/00397919608003767

This article was downloaded by: [Computing & Library Services, University
of Huddersfield]
On: 04 January 2015, At: 08:55
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
1,3-Dipolar Cycloaddition
Reactions of C-(2-Nitro)-styryl-
N-phenyl Nitrone Leading
to the Regiospecific and
Stereospecific Synthesis of New
Isoxazolidine Derivatives
a
K. Krishan Singal
a
Department of Chemistry , Punjabi University ,
Patiala, 147002, India
Published online: 21 Aug 2006.
To cite this article: K. Krishan Singal (1996) 1,3-Dipolar Cycloaddition Reactions of
C-(2-Nitro)-styryl-N-phenyl Nitrone Leading to the Regiospecific and Stereospecific
Synthesis of New Isoxazolidine Derivatives, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 26:19,
3571-3577, DOI: 10.1080/00397919608003767
To link to this article: http://dx.doi.org/10.1080/00397919608003767
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