First 1,3-dipolar cycloaddition of Z-α-phenyl-N-methylnitrone with allylic fluorides: a stereoselective route to enantiopure fluorine-containing isoxazolidines and amino polyols
摘要:
Enantiopure fluorinated isoxazolidines and amino polyols were obtained from the 1,3-dipolar cycloaddition of allylic fluorides and Z-alpha-phenyl-N-methylnitrone under environment-friendly conditions. (C) 2003 Elsevier Ltd. All right reserved.
First 1,3-dipolar cycloaddition of Z-α-phenyl-N-methylnitrone with allylic fluorides: a stereoselective route to enantiopure fluorine-containing isoxazolidines and amino polyols
摘要:
Enantiopure fluorinated isoxazolidines and amino polyols were obtained from the 1,3-dipolar cycloaddition of allylic fluorides and Z-alpha-phenyl-N-methylnitrone under environment-friendly conditions. (C) 2003 Elsevier Ltd. All right reserved.
First 1,3-dipolar cycloaddition of Z-α-phenyl-N-methylnitrone with allylic fluorides: a stereoselective route to enantiopure fluorine-containing isoxazolidines and amino polyols
作者:Luca Bernardi、Bianca F. Bonini、Mauro Comes-Franchini、Mariafrancesca Fochi、Mahena Folegatti、Stefano Grilli、Andrea Mazzanti、Alfredo Ricci
DOI:10.1016/j.tetasy.2003.11.008
日期:2004.1
Enantiopure fluorinated isoxazolidines and amino polyols were obtained from the 1,3-dipolar cycloaddition of allylic fluorides and Z-alpha-phenyl-N-methylnitrone under environment-friendly conditions. (C) 2003 Elsevier Ltd. All right reserved.