113231-48-4Relevant academic research and scientific papers
Regioselective palladium-catalyzed decarboxylative cross-coupling reaction of alkenyl acids with coumarins: Synthesis of 3-styrylcoumarin compounds
Wang, Xu,Li, Shen-Yan,Pan, Ying-Ming,Wang, Heng-Shan,Chen, Zhen-Feng,Huang, Ke-Bin
, p. 2407 - 2412 (2015/04/27)
A novel and efficient protocol for the regioselective synthesis of 3-styrylcoumarins from readily available cinnamic acids and coumarins is presented. The reaction proceeds via a decarboxylative cross-coupling mediated by a catalytic amount of Pd(OAc)2, with Ag2CO3 as an oxidant, and with 1,10-phenanthroline as a ligand. A plausible reaction mechanism for this process is depicted, and the resulting 3-styrylcoumarins show excellent fluorescence quantum yields.
Snythesis of 3-Styrylcoumarins from Coumarin-3-acetic Acids and 3-Phenacylcoumarins
Chodankar, N. K.,Joshi, S. D.,Sequeria, S.,Seshadri, S.
, p. 427 - 430 (2007/10/02)
The hitherto unknown 3-styrylcoumarin system has been synthesised by two routes.In the first approach, coumarin-3-acetic acids are reacted with aromatic aldehydes to yield directly the 3-styrylcoumarins.The synthesis is limited by the difficulty in obtaining coumarin-3-acetic acids in good yields.The second approach utilises 3-phenacylcoumarins which are reduced to the carbinols and subsequently dehydrated to the corresponding 3-styrylcoumarins.The fluorescence of these compounds and their application to polyester fibre have been studied.
