Effects of 17-alkyl-16,17-dihydrogibberellin A(5) derivatives on growth and flowering in Lolium temulentum

Citation
Ln. Mander et al., Effects of 17-alkyl-16,17-dihydrogibberellin A(5) derivatives on growth and flowering in Lolium temulentum, PHYTOCHEM, 49(6), 1998, pp. 1509-1515
Citations number
11
Categorie Soggetti
Agricultural Chemistry","Animal & Plant Sciences
Journal title
PHYTOCHEMISTRY
ISSN journal
00319422 → ACNP
Volume
49
Issue
6
Year of publication
1998
Pages
1509 - 1515
Database
ISI
SICI code
0031-9422(199811)49:6<1509:EO1ADO>2.0.ZU;2-1
Abstract
Several gibberellins in which the 16-methyl group of the 16-epimers of dihy dro-GA(5) had been replaced by ethyl, n-propyl and n-butyl were prepared an d tested at doses of 1, 5 or 25 mu g per plant for their effects on stem gr owth and flowering of the grass Lolium temulentum. The ethyl and n-propyl d erivatives were most inhibitory of elongation, the exo-isomers being more a ctive than the endo-forms. While both isomers of dihydro-GAS promoted flowe ring, among the 17-alkyl analogues, only the exo-ethyl derivative showed si gnificant activity. (C) 1998 Published by Elsevier Science Ltd. All rights reserved.