Issue 12, 2010
From the journal:

Chemical Communications

Concise total synthesis of naamine G and naamidine H†

Panduka B. Koswattaa  and  Carl J. Lovely*a  

* Corresponding authors

a Department of Chemistry and Biochemistry, The University of Texas at Arlington, Arlington, USA
E-mail: lovely@uta.edu
Fax: +1 817-272-3808
Tel: +1 817-272-5446

Abstract

Total syntheses of the cytotoxic Leucetta-derived 2-aminoimidazoles, naamine G and naamidine H, have been accomplished using a position selective metalation–benzylation sequence with a 4,5-diiodoimidazole derivative.

Graphical abstract: Concise total synthesis of naamine G and naamidine H

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Article information

DOI
https://doi.org/10.1039/B926285G
Article type
Communication
Submitted
14 Dec 2009
Accepted
22 Jan 2010
First published
09 Feb 2010

Chem. Commun., 2010,46, 2148-2150

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Concise total synthesis of naamine G and naamidine H

P. B. Koswatta and C. J. Lovely, Chem. Commun., 2010, 46, 2148 DOI: 10.1039/B926285G

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