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
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