Flowers of Aglaia duperreana collected in Vietnam yielded thirteen insectic
idal cyclopentatetrahydrobenzofuran derivatives of the rocaglamide type inc
luding five compounds which proved to be new natural products. Structure el
ucidation of the new compounds and their insecticidal activity against larv
ae of the pest insect Spodoptera littoralis are described. Most of the isol
ated rocaglamide derivatives exhibited strong to moderate insecticidal acti
vity. The most active compounds were similar with regard to their bioactivi
ty to the well known natural insecticide azadirachtin, However, replacement
of the OH-group at C-8b (that is a characteristic structural feature of mo
st known rocaglamide congeners) by an OC2H5-substituent as present in two o
f the isolated new derivatives was found to result in a loss of insecticida
l activity. (C) 1999 Elsevier Science Ltd. All rights reserved.