838-58-4Relevant articles and documents
Carboxylic acid addition to terminal alkynes utilizing ammonium tagged Hoveyda-Grubbs catalyst supported on magnetically separable core/shell silica: A highly reusable and air compatible catalytic system
?ztürk, Bengi ?zgün,Gürcü, Didar,?ehito?lu, Solmaz Karabulut
, p. 11 - 16 (2019/01/24)
In this study, the performance of ammonium tagged Hoveyda-Grubbs catalyst supported on magnetically separable core/shell silica gel was tested on carboxylic acid addition reactions to terminal alkynes using a variety of carboxylic acid derivatives under air atmosphere. The catalytic system was found to be compatible with air atmosphere and can tolerate even non-degassed solvents. The reaction parameters such as temperature, substrate/catalyst ratio and the effect of carboxylic acid on the selectivity and yield of the reaction were investigated in details. The reaction of arylacetylenes with acetic acid yielded the corresponding E-isomer with conversion values up to 99% with a catalytic loading of 1% Ru. The reusability of the catalyst was tested using acetic acid/benzoic acid and phenylacetylene in toluene at 85 °C under air atmosphere. The catalyst was found to be highly reusable and maintained its activity up to 11th run, reaching a conversion value of 83% with minimum ruthenium leaching.
Enol Ester Synthesis via Cobalt-Catalyzed Regio- and Stereoselective Addition of Carboxylic Acids to Alkynes
Chen, Jia-Feng,Li, Changkun
supporting information, p. 6719 - 6724 (2018/11/21)
A cobalt-catalyzed highly regio- and stereoselective hydro-oxycarbonylation of alkynes is reported. Both terminal and internal alkynes can react with carboxylic acids to afford enol esters in high yields. The catalyst generated from Co(BF4)2, tridentate phosphine ligand L5, and zinc in situ exhibits much higher reactivity than the corresponding cobalt/diphosphine complex.
Alkyne reactions with trimethylphosphine complexes of iridium: Lessons for the catalysis of vinyl ester formation and alkyne dimerization
Merola, Joseph S.,Ladipo, Folami T.
, p. 125 - 132 (2014/02/14)
The combination of iridium with trimethylphosphine ligands yields very electron rich iridium compounds that are active for terminal alkyne dimerization chemistry as well as the addition of carboxylic acids to alkynes. The structures, catalytic and stoichi
