Monatshefte fur Chemie p. 99 - 110 (1985)
Update date:2022-08-03
Topics:
Wawrzenczyk, Czeslaw
Lochynski, Stanislaw
New cyclic juvenoids containing the 3,3-dimethylcyclohexane (esters 16, 18, 22, 26, and ehters 28a,b) or the 5,5-dimethyl-2-cyclohexene system (esters 15, 17, 21, 25, and ehters 27a,b) have been obtained by a several-step synthesis starting from dimedone (1).The compounds obtained exhibited morphogenetic activity against larvae of Dysdercus cingulatus and they were inactive on pupae of Tenebrio molitor.Keywords: Claisen rearrangement; gem-Dimethylcyclohexane derivatives; Juvenoids
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Doi:10.1016/S0040-4039(00)87682-0
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