99277-36-8Relevant academic research and scientific papers
INTRAMOLECULAR MICHAEL ADDITION REACTION TO CHIRAL VINYLIC SULFOXIDES. AN ENANTIOSELECTIVE SYNTHESIS OF (R)- AND (S)-1,7-DIOXASPIROUNDECANE
Iwata, Chuzo,Fujita, Masahiro,Hattori, Kohji,Uchida, Shuji
, p. 2221 - 2224 (1985)
(R)- and (S)-1,7-Dioxaspiroundecane , sex pheromone of an olive fly, was each stereoselectively synthesized using an intramolecular Michael addition of hydroxyl group to a chiral vinylic sulfoxide moiety as an asymmetric induction step.
