Several enantiopure 1,2-amino alcohols have been prepared by combining a stereoselective enzymatic epoxidation of styrenes with regio- and stereoselective chemical reactions. An interesting reactivity has been noted concerning the reaction of epoxides and NH3 under microwave activation

Sello, G., Orsini, F., Bernasconi, S., DI GENNARO, P. (2006). Synthesis of enantiopure 2-amino-1-phenyl and 2-amino-2-phenyl ethanols using enantioselective enzymatic epoxidation and regio-and diastereoselective chemical aminolysis. TETRAHEDRON-ASYMMETRY, 17(3), 372-376 [10.1016/j.tetasy.2006.01.009].

Synthesis of enantiopure 2-amino-1-phenyl and 2-amino-2-phenyl ethanols using enantioselective enzymatic epoxidation and regio-and diastereoselective chemical aminolysis

DI GENNARO, PATRIZIA
2006

Abstract

Several enantiopure 1,2-amino alcohols have been prepared by combining a stereoselective enzymatic epoxidation of styrenes with regio- and stereoselective chemical reactions. An interesting reactivity has been noted concerning the reaction of epoxides and NH3 under microwave activation
Articolo in rivista - Articolo scientifico
epoxidation, enantioselective enzymatic reactions, biocatalysis
English
2006
17
3
372
376
none
Sello, G., Orsini, F., Bernasconi, S., DI GENNARO, P. (2006). Synthesis of enantiopure 2-amino-1-phenyl and 2-amino-2-phenyl ethanols using enantioselective enzymatic epoxidation and regio-and diastereoselective chemical aminolysis. TETRAHEDRON-ASYMMETRY, 17(3), 372-376 [10.1016/j.tetasy.2006.01.009].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/15211
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