Abstract
A four-stage synthesis has been performed of the optically active (S)-(−)-diprionyl acetate in the form of an equimolar mixture of erythro-(2S,3S,7SR)- and threo-(2R,3S,7SR)-2-acetoxy-3,7-dimethylpentadecanes from a readily available chiral compound — (S)-(+)-3,7-dimethylocta-1,6-diene — with an overall yield of 13%.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
