Synthesis and cytokinin activity of two fluoro derivatives of n(6)-isopentenyladenine

被引：18

作者：

Clemenceau, D

Cousseau, J

Martin, V

Molines, H

Wakselman, C

Mornet, R

Nogue, F

Laloue, M

机构：

[1] FAC SCI,LAB INGN MOLEC & MAT ORGAN,F-49045 ANGERS,FRANCE

[2] CERCOA,F-94320 THIAIS,FRANCE

[3] INRA,BIOL CELLULAIRE LAB,F-78026 VERSAILLES,FRANCE

来源：

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY | 1996年 / 44卷 / 01期

关键词：

cytokinins; fluoro compounds; biological activity;

D O I：

10.1021/jf9501148

中图分类号：

S [农业科学];

学科分类号：

09 ;

摘要：

Two derivatives of N-6-isopentenyladenine, 3 and 4, bearing either a vinylic fluorine atom or a trifluoromethyl group, were easily synthesized from known fluorinated precursors. Both derivatives 3 and 4 were found to be more active, as cytokinins, than the parent compounds zeatin (1) and N-6-isopentenyladenine (2).

引用

页码：320 / 323

页数：4

共 24 条

[1] SYNTHESES OF ORGANOFLUORINE COMPOUNDS .8. SOLVOLYTIC RING-OPENING OF ALKOXYCHLOROFLUOROCYCLOPROPANES - READY ACCESS TO FLUORINATED ALPHA-BETA-UNSATURATED ALDEHYDES AND KETONES [J].