299430-04-9Relevant academic research and scientific papers
Pheromone synthesis, CCIS synthesis of the enantiomers of anti-2,6-dimethylheptane-1,7-diol monotetrahydropyranyl ether and their conversion into the enantiomers of the sex pheromone components of the apple leafminer, Lyonetia prunifoliella
Nakamura, Yoshihide,Mori, Kenji
, p. 2745 - 2753 (2007/10/03)
Both (2R,6R)- and (2S,6S)-isomers of 2,6-dimethylheptane-1,7-diol monotetrahydropyranyl ether (4) were synthesized, and converted into the enantiomers of anti-10,14-dimethyl-1-octadecene (1), anti-5,9-dimethyloctadecane (2) and anti-5,9-dimethylheptadecane (3), the sex pheromone components of the apple leafminer (Lyonetia prunifoliella).
TOTAL SYNTHESIS OF A PUTATIVE TRIENE INTERMEDIATE IN MONENSIN BIOSYNTHESIS, ACTIVATED AS A CAPRYLCYSTEAMINE THIOL ESTER.
Holmes, Duncan S.,Dyer, Ulrich C.,Russell, Simon,Sherringham, John A.,Robinson, John A.
, p. 6357 - 6360 (2007/10/02)
The total synthesis is reported, from a pool of optically pure starting materials, of a tritium labelled form of a putative intermediate in monensin biosynthesis, in which the terminal carboxyl group is activated as a caprylcysteamine thiol ester.
