Nitrones in organic synthesis. Synthesis of secondary allyl amines

Article abstract of DOI:10.1080/00397919408010566

Nitrones 1 undergo addition of vinyl organomagnesium bromide to give the allyl hydroxylamines 3 which are easily reduced to the corresponding N-benzyl allyl amines 2.

Full text of DOI:10.1080/00397919408010566

This article was downloaded by: [New York University]
On: 20 July 2015, At: 05:44
Publisher: Taylor & Francis
Informa Ltd Registered in England and Wales Registered Number: 1072954
Registered office: 5 Howick Place, London, SW1P 1WG
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
Nitrones in Organic Synthesis.
Synthesis of Secondary Allyl
Amines
A. Dondoni a , F. L. Merchán b , P. Merino a & T.
Tejero b
a Laboratorio di Chimica Organica Dipartimento di
Chimica. Università , I-44100, Ferrara, Italy
b Departamento de Química Orgánica , ICMA.
Universidad de Zaragoza , E-50009, Zaragoza, Spain
Published online: 23 Sep 2006.
To cite this article: A. Dondoni , F. L. Merchán , P. Merino & T. Tejero (1994) Nitrones
in Organic Synthesis. Synthesis of Secondary Allyl Amines, Synthetic Communications:
An International Journal for Rapid Communication of Synthetic Organic Chemistry,
24:18, 2551-2555, DOI: 10.1080/00397919408010566
To link to this article: http://dx.doi.org/10.1080/00397919408010566
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