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_kinetically_2011,
	title = {Kinetically controlled synthesis of monoglyceryl esters from chiral and prochiral acids methyl esters catalyzed by immobilized {Rhizomucor} miehei lipase},
	volume = {102},
	url = {http://linkinghub.elsevier.com/retrieve/pii/S096085241001480X},
	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},
	language = {English},
	number = {2},
	journal = {Bioresource Technology},
	author = {Acosta, Andreina and Filice, Marco and Fernandez-Lorente, Gloria and Palomo, Jose M and Guisan, Jose M},
	month = jan,
	year = {2011},
	pages = {507--512}
}