864360-37-2Relevant academic research and scientific papers
Regioselective nucleophilic opening of azetidinium ions
Couty, Fran?ois,Durrat, Fran?ois,Evano, Gwilherm
, p. 1666 - 1670 (2005)
Azetidinium ions bearing different substitution patterns were reacted with nitrogen nucleophiles (sodium azide and benzylamine) and oxygenated nucleophiles (sodium acetate and alkoxides). High regioselectivity of nucleophilic opening was observed in both
Nucleophilic ring-opening of azetidinium ions: Insights into regioselectivity
Couty, Fran?ois,David, Olivier,Durrat, Fran?ois,Evano, Gwilherm,Lakhdar, Sami,Marrot, Jérome,Vargas-Sanchez, Monica
, p. 3479 - 3490 (2007/10/03)
Enantiopure azetidinium salts presenting various and representative substitution patterns at C-2, C-3 and C-4 have been prepared by alkylation of the corresponding azetidine with methyl trifluoromethanesulfonate. These compounds were treated with an array
