A new methodology for synthesis of 1,2-epoxy alkane with the linear aliphatic olefins in presence of molecular oxygen

Article abstract of DOI:10.1080/00397919908086118

The linear aliphatic olefins, such as 1-octene, 1-decene, 1-dodecene and 1-tetradecene, were effectively epoxidized with molecular oxygen catalyzed by the amino acid Schiff base manganese complex (Sal-Phe-Mn). The products of the reaction was 1,2-epoxy alkane.

Full text of DOI:10.1080/00397919908086118

This article was downloaded by: [University of Connecticut]
On: 11 October 2014, At: 18:33
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
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 New Methodology for
Synthesis of 1,2-Epoxy Alkane
with the Linear Aliphatic
Olefins in Presence of
Molecular Oxygen
Rong-Min Wang a , Cheng-Jun Hao a & Yun-Pu Wang a
a Department of Chemistry , Northwest Normal
University , Lanzhou, 730070, P.R. China
Published online: 17 Sep 2007.
To cite this article: Rong-Min Wang , Cheng-Jun Hao & Yun-Pu Wang (1999) A New
Methodology for Synthesis of 1,2-Epoxy Alkane with the Linear Aliphatic Olefins in
Presence of Molecular Oxygen, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 29:8, 1409-1414, DOI:
10.1080/00397919908086118
To link to this article: http://dx.doi.org/10.1080/00397919908086118
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