222546-56-7Relevant academic research and scientific papers
Enantioselective total synthesis of cis-(+)- and trans-(+)-disparlure
Garg, Yuvraj,Kumar Tiwari, Anand,Kumar Pandey, Satyendra
, p. 3344 - 3346 (2017)
An expedient enantioselective synthetic approach for the gypsy moth sex-attractant pheromone cis-(+)-1 and trans-(+)-disparlure 2 is described employing the optimized combination of organocatalytic MacMillan's self aldol reaction, Wittig olefination, regioselective ring opening of an epoxide and Mitsunobu esterification reactions as key steps.
