TY - JOUR
AU - Bhattacharjee, Manish
AB - O‐Dienyl esters are obtained through the regio‐ and stereospecific addition of both aromatic and aliphatic carboxylic acids to terminal propargylic alcohols, with the sequential formation of a carbon–oxygen bond and dehydration, in the presence of [(p‐cymene)Ru(dppp)Cl][PF6] (1). Also, the cytotoxicity and anticancer activity of the newly synthesized O‐dienyl ester (Z)‐3‐methylbuta‐1,3‐dienyl oleate have been investigated.
TI - [(para‐Cymene)Ru(dppp)Cl][PF6]‐Catalysed Stereospecific Synthesis of O‐Dienyl Esters, and Evaluation of the Anticancer Activity of a Long‐Chain Fatty Acid O‐Dienyl Ester
JF - European Journal of Organic Chemistry
DO - 10.1002/ejoc.201601557
DA - 2017-03-17
UR - https://www.deepdyve.com/lp/wiley/para-cymene-ru-dppp-cl-pf6-catalysed-stereospecific-synthesis-of-o-wow9rep7UO
SP - 1514
EP - 1519
VL - 2017
IS - 11
DP - DeepDyve
ER -