INHIBITION OF BOTRYTIS-CINEREA BY NEW SESQUITERPENOID COMPOUNDS OBTAINED FROM THE REARRANGEMENT OF ISOCARYOPHYLLENE

Authors
COLLADO IG ALEU J MACIASSANCHEZ AJ HERNANDEZGALAN R
Citation
Ig. Collado et al., INHIBITION OF BOTRYTIS-CINEREA BY NEW SESQUITERPENOID COMPOUNDS OBTAINED FROM THE REARRANGEMENT OF ISOCARYOPHYLLENE, Journal of natural products, 57(6), 1994, pp. 738-746
Citations number
11
Categorie Soggetti
Chemistry,"Plant Sciences","Pharmacology & Pharmacy
Journal title
Journal of natural products → ACNP
ISSN journal
01633864
Volume
57
Issue
6
Year of publication
1994
Pages
738 - 746
Database
ISI
SICI code
0163-3864(1994)57:6<738:IOBBNS>2.0.ZU;2-#
Abstract
A careful study of the acid-catalyzed cyclization of isocaryophyllene has provided new information on the reaction mechanism. A novel sesqui terpene skeletal type has resulted from unusual rearrangements of isoc aryophyllene. The alcohols ginsenol [9] and 4 beta,8 ramethyl-11-hydro xytricyclo[6,2,1,0(4,11)]undecane [10] were found to inhibit the growt h of Botrytis cinerea in vitro.