The stereoselective synthesis of dienyl esters with high
atom-
and step-economy has been largely unexplored. Herein, we report an
efficient approach for the synthesis of E-dienyl
esters via rhodium catalysis using carboxylic acid and acetylene as
C2 synthon through the cascade of cyclometalation and C–O coupling.
This protocol features mild conditions, excellent functional group
tolerance, and exclusive E-stereoselectivity and
utility in the late-stage modification of pharmaceuticals and natural
products.