Enantiospecific syntheses of the potent bioactives nagilactone F and the mould metabolite LL-Z1271 alpha an evaluation of their allelopathic potential

Authors
Barrero, AF Sanchez, JF Elmerabet, J Jimenez-Gonzalez, D Macias, FA Simonet, AM
Citation
Af. Barrero et al., Enantiospecific syntheses of the potent bioactives nagilactone F and the mould metabolite LL-Z1271 alpha an evaluation of their allelopathic potential, TETRAHEDRON, 55(23), 1999, pp. 7289-7304
Citations number
19
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
55
Issue
23
Year of publication
1999
Pages
7289 - 7304
Database
ISI
SICI code
0040-4020(19990604)55:23<7289:ESOTPB>2.0.ZU;2-0
Abstract
Improved syntheses are described for nagilactone F and the antibiotic LL-Z1 271 alpha, two of the most potent bioactive members of the podolactone fami ly. The allelopathic potential of some members of this podolactone series h as been evaluated, with the result that the metabolite LL-Z1271 alpha is on e of the most active compounds. (C) 1999 Elsevier Science Ltd. All rights r eserved.