Twigs of Aglaia duppereana collected in Vietnam yielded the cyclopenta
tetrahydrobenzofuran, rocaglamide, and also six of its congeners. Wher
eas three of the isolated compounds were already known, four rocaglami
de derivatives were new natural products. Elucidation of their structu
res and absolute configurations is described. All the rocaglamide deri
vatives isolated exhibited strong insecticidal activity towards neonat
e larvae of the polyphagous pest insect Spodoptera littoralis when inc
orporated into artificial diet. The LC(50) for rocaglamide, which was
one of the most active compounds encountered in this study, was 0.9 pp
m, identical to that of azadirachtin used as a positive control in fee
ding experiments. Copyright (C) 1997 Elsevier Science Ltd.