Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4167
Title: Ring opening of phenylaziridines with allylsilanes.
Authors: M. R., Schneider
A., Mann
Taddei, Maurizio 
Issue Date: 1996
Project: None 
Journal: TETRAHEDRON LETTERS
Abstract: 
N-tosyl phenylaziridines are opened regioselectively with allylsilanes in presence of BF3.Et(2)O to form gamma-amino olefins. During the reaction a formal [3+2] cycloaddition produced the corresponding pyrrolidines, amenable to the open chain compounds with TBAF. Copyright (C) 1996 Published by Elsevier Science
Description: 
45963
URI: http://hdl.handle.net/20.500.12779/4167
ISSN: 0040-4039
DOI: 10.1016/0040-4039(96)01975-2
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