Ring opening of homochiral bicyclic oxazolidinones: Synthesis of allylglycinol derivatives

Article abstract of DOI:10.1080/00397919808006837

(4R,6aS)-2-Oxo-4-phenyl-2,4,5,6a,7-hexahydrooxazolo[3,2-c]oxazole and its 4-methyl analog were synthesized using (R)-phenylglycinol and (S)- alaninol as the chiral source, respectively. The ring opening reaction of the bicyclic oxazolidinones by an allylt

Full text of DOI:10.1080/00397919808006837

This article was downloaded by: [New York University]
On: 27 April 2015, At: 12:17
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
Ring Opening of Homochiral
Bicyclic Oxazolidinones:
Synthesis of Allylglycinol
Derivatives
Sung-Gon Kim a & Kyo Han Ahn a
a Department of Chemistry and Center for
Biofunctional Molecules , POSTECH , San 31 Hyoja-
dong, Pohang, 790-784, Korea
Published online: 22 Aug 2006.
To cite this article: Sung-Gon Kim & Kyo Han Ahn (1998) Ring Opening of
Homochiral Bicyclic Oxazolidinones: Synthesis of Allylglycinol Derivatives, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 28:8, 1387-1397, DOI: 10.1080/00397919808006837
To link to this article: http://dx.doi.org/10.1080/00397919808006837
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