Stereoselective construction of the azabicyclic core applicable to the biologically important polyguanidinium alkaloids batzelladine A and D using a free radical cyclization

Authors
Evans, PA Manangan, T
Citation
Pa. Evans et T. Manangan, Stereoselective construction of the azabicyclic core applicable to the biologically important polyguanidinium alkaloids batzelladine A and D using a free radical cyclization, TETRAHEDR L, 42(38), 2001, pp. 6637-6640
Citations number
28
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
42
Issue
38
Year of publication
2001
Pages
6637 - 6640
Database
ISI
SICI code
0040-4039(20010917)42:38<6637:SCOTAC>2.0.ZU;2-6
Abstract
The intramolecular addition of the free radical derived from the alkyl brom ide 13 provides an expeditious and stereoselective approach to the azabicyc lic core 14, which is applicable to the biologically important polyguanidin ium alkaloids batzelladine A (1) and D (2). (C) 2001 Published by Elsevier Science Ltd.