by Acosta, Andreina, Filice, Marco, Fernandez-Lorente, Gloria, Palomo, Jose M and Guisan, Jose M
Abstract:
Partial acylation of only one primary hydroxyl group of glycerol generates a chiral center at position 2. Rhizomucor miehei lipase (RML) catalyzes the kinetically controlled transesterification of different aromatic carboxylic acids methyl esters with glycerol. High
Reference:
Kinetically controlled synthesis of monoglyceryl esters from chiral and prochiral acids methyl esters catalyzed by immobilized Rhizomucor miehei lipase (Acosta, Andreina, Filice, Marco, Fernandez-Lorente, Gloria, Palomo, Jose M and Guisan, Jose M), In Bioresource Technology, volume 102, 2011.
Bibtex Entry:
@article{Acosta:2011di,
author = {Acosta, Andreina and Filice, Marco and Fernandez-Lorente, Gloria and Palomo, Jose M and Guisan, Jose M},
title = {{Kinetically controlled synthesis of monoglyceryl esters from chiral and prochiral acids methyl esters catalyzed by immobilized Rhizomucor miehei lipase}},
journal = {Bioresource Technology},
year = {2011},
volume = {102},
number = {2},
pages = {507--512},
month = jan,
language = {English},
rating = {0},
date-added = {2017-08-22T10:48:19GMT},
date-modified = {2020-07-09T13:27:50GMT},
abstract = {Partial acylation of only one primary hydroxyl group of glycerol generates a chiral center at position 2. Rhizomucor miehei lipase (RML) catalyzes the kinetically controlled transesterification of different aromatic carboxylic acids methyl esters with glycerol. High 
},
url = {http://linkinghub.elsevier.com/retrieve/pii/S096085241001480X},
uri = {url{papers3://publication/uuid/4511F2D9-2EBF-4871-8584-C6C145531419}}
}