PRACTICAL SYNTHESIS OF UNSYMMETRICAL POLYAMINE AMIDES

Citation
Is. Blagbrough et Aj. Geall, PRACTICAL SYNTHESIS OF UNSYMMETRICAL POLYAMINE AMIDES, Tetrahedron letters, 39(5-6), 1998, pp. 439-442
Citations number
39
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
39
Issue
5-6
Year of publication
1998
Pages
439 - 442
Database
ISI
SICI code
0040-4039(1998)39:5-6<439:PSOUPA>2.0.ZU;2-E
Abstract
Desymmetrisation of readily available symmetrical polyamines is an imp ortant first step in the synthesis of many polyamine containing natura l products. Likewise in the synthesis of polyamine amides which are po tentially useful for gene delivery and as neuroprotectants, based upon channel blocking toxins found in certain wasp and spider venoms. The application of trifluoroacetyl as a protecting group allows unsymmetri cal polyamine amides to be easily prepared on a gram scale. (C) 1997 E lsevier Science Ltd. All rights reserved.