A convenient and efficient process to 5-(2-Di-n-propylaminoethyl)-6-hydroxyindole

Article abstract of DOI:10.1080/00397919408011708

An intermolecular trapping of the Pummerer intermediate, generated from 9 with TFAA, by 4 at position 5 under mild Lewis acid conditions gave S. Sequential treatment of 5 with Ra-Ni, LiAlH₄ and again Ra-Ni, afforded 8 in high overall yield.

Full text of DOI:10.1080/00397919408011708

This article was downloaded by: [Michigan State University]
On: 06 January 2015, At: 15:10
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 Convenient and Efficient
Process to 5-(2-Di-n-
Propylaminoethyl)-6-
hydroxyindole
Christos G. Gourdoupis a , Heleni K. Kotzamani a &
Ionnis K. Stamos b c
a University of Patras, School of Health Sciences,
Department of Pharmacy , Rion, Patras, 261 10,
Hellas
b The National Hellenic Research Foundation ,
Institute of Organic and Pharmaceutical Chemistry
and the Center for Molecular Analysis , 48 V.
Konstantinou Ave., Athens, 116 35, Hellas
c University of Patras, Department of Pharmacy ,
Rion, Patras, 261 10, Hellas
Published online: 23 Sep 2006.
To cite this article: Christos G. Gourdoupis , Heleni K. Kotzamani & Ionnis K.
Stamos (1994) A Convenient and Efficient Process to 5-(2-Di-n-Propylaminoethyl)-6-
hydroxyindole, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 24:8, 1129-1136, DOI:
10.1080/00397919408011708
To link to this article: http://dx.doi.org/10.1080/00397919408011708

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