Enantiospecific syntheses of the potent bioactives nagilactone F and the mould metabolite LL-Z1271α an evaluation of their allelopathic potential

被引：21

作者：

Barrero, AF

Sánchez, JF

Elmerabet, J

Jiménez-González, D

Macías, FA

Simonet, AM

机构：

[1] Univ Granada, Fac Ciencias, Inst Biotecnol, Dept Quim Organ, E-18071 Granada, Spain

[2] Univ Cadiz, Fac Ciencias, Dept Quim Organ, Puerto Real 11510, Cadiz, Spain

来源：

TETRAHEDRON | 1999年 / 55卷 / 23期

关键词：

podolactones; synthesis; herbicides;

D O I：

10.1016/S0040-4020(99)00355-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Improved syntheses are described for nagilactone F and the antibiotic LL-Z1271 alpha, two of the most potent bioactive members of the podolactone family. The allelopathic potential of some members of this podolactone series has been evaluated, with the result that the metabolite LL-Z1271 alpha is one of the most active compounds. (C) 1999 Elsevier Science Ltd. All rights reserved.

引用

页码：7289 / 7304

页数：16

共 19 条

[1]

ADINOLFI M, 1973, GAZZ CHIM ITAL, V103, P1271

[2] C-13 NMR DATA FOR LABDANE DITERPENOIDS [J].