Enantiopure fluorinated isoxazolidines and amino polyols were obtained from the 1,3-dipolar cycloaddition of allylic fluorides and Z-α-phenyl-N-methylnitrone under environment-friendly conditions
BERNARDI L., BONINI B.F., COMES-FRANCHINI M., FOCHI M., FOLEGATTI M., GRILLI S., et al. (2004). First 1,3-dipolar Cycloaddtion of Z-alfa-phenyl-N-methylnitrone with Allylic Fluorides: a Stereoselective Route to Enantiopure Fluorine-Contaning Isoxazolidines and Amino Polyols. TETRAHEDRON-ASYMMETRY, 15, 245-250 [10.1016/j.tetasy.2003.11.008].
First 1,3-dipolar Cycloaddtion of Z-alfa-phenyl-N-methylnitrone with Allylic Fluorides: a Stereoselective Route to Enantiopure Fluorine-Contaning Isoxazolidines and Amino Polyols
BERNARDI, LUCA;BONINI, BIANCA FLAVIA;COMES FRANCHINI, MAURO;FOCHI, MARIAFRANCESCA;GRILLI, STEFANO;MAZZANTI, ANDREA;RICCI, ALFREDO MARCO
2004
Abstract
Enantiopure fluorinated isoxazolidines and amino polyols were obtained from the 1,3-dipolar cycloaddition of allylic fluorides and Z-α-phenyl-N-methylnitrone under environment-friendly conditionsFile in questo prodotto:
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