24112-71-8Relevant academic research and scientific papers
Lipase-catalyzed regioselective monoacetylation of unsymmetrical 1,5-primary diols
Oger, Camille,Marton, Zsuzsanna,Brinkmann, Yasmin,Burtel-Ponce, Valerie,Durand, Thierry,Graber, Marianne,Galano, Jean-Marie
supporting information; experimental part, p. 1892 - 1897 (2010/05/19)
"Chemical Equation Presented" Lipase B from Candida antarctica (CALB) has been selected as the most suitable enzyme to catalyze the regioselective monoacetylation of 1,5-diol isoprostane intermediate, using vinyl acetate as an acyl transfer reagent in TIIF. We next applied this reaction on linear 2-substituted, 2,2′-disubstituted-l,5pentanediols, and, cyclic 2,3-disubstituted-l,5-pentanediols. To rationalize the regioselectivity observed, molecular docking simulations were performed.
The Stereochemistry of Organometallic Compounds. XXXVIII. Regio- and Stereo-control in the Rhodium-Catalysed Hydroformylation of Some Alkenyl Phosphites
Jackson, W. Roy,Moffat, Mark R.,Perlmutter, Patrick,Tasdelen, E. Elizabeth
, p. 823 - 834 (2007/10/02)
Excellent regiocontrol is achieved in the rhodium-catalysed hydroformylation of some alkenyl phosphites, and good stereocontrol is obtained in the hydroformylation of some cyclohexenyl phosphites.The stereochemical results have implications for the mechanism of these rhodium-catalysed reactions.
