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
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 L.; BONINI B.F.; COMES-FRANCHINI M.; FOCHI M.; FOLEGATTI M.; GRILLI S.; MAZZANTI A.; RICCI A.;. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - STAMPA. - 15:(2004), pp. 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:
Eventuali allegati, non sono esposti
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
