Abstract
AbstractThe stereochemical course of β‐oxygen elimination of an organorhodium(I) complex was investigated through the Rh‐catalyzed addition of phenylboronic acid to a chiral propargyl acetate to produce an allene. The degree of chirality transfer suggests that the β‐oxygen elimination takes place in both syn and anti modes.
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
