Journal of Organic Chemistry p. 2366 - 2369 (1990)
Update date:2022-08-04
Topics:
Ottolina, Gianluca
Carrea, Giacomo
Riva, Sergio
Regioselective esterification of chloramphenicol (1) and its synthetic analogue thiamphenicol (2) has been achieved by the action of lipase in acetone and several methyl carboxylates.Aliphatic and aromatic esters of different sizes and natures have been introduced selectively on the primary hydroxyl group of these molecules by modification of the reaction conditions (e.g., temperature, solvent, and lipase source).
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