
%0 Journal Article
%A Cavill, GWK 
%A Whitfield, FB 
%T Insect venoms, attractants, and repellents. VI. Synthesis of the dolichodials
%J Australian Journal of Chemistry
%D 1964/11/01
%V 17
%N 11
%P 1260-1269
%K 
%R https://doi.org/10.1071/CH9641260
%U https://www.publish.csiro.au/paper/CH9641260 
%X The cis-trans, trans-cis, and trans-trans-dolichodials (II, III, and IV) have been synthesized from the ethylene acetal of ethyl &#945;-(2-formyl-3-methylcyclopentyl)-cyanoacetate, a transformation product of D-(+)-citronellal. The cis-trans and trans-cis-isomers (II and III) are enantiomers of the natural dolichodial. 
