101101-38-6Relevant articles and documents
Use of highly stereospecific 1,3-dipolar cycloadditions of cyclic nitrones with acetylenes in the preparation of novel heterocyclic ring systems
Bowman, W. Russell,Davies, Roy V.,Slawin, Alexandra M. Z.,Sohal, Gian S.,Titman, Roger B.,Wilkins, David J.
, p. 155 - 161 (2007/10/03)
Cyclic nitrones with substituents a to the nitrogen atom undergo 1,3-dipolar cycloadditions in a stereo-and regio-specific manner with acetylenes. The nitrone 3 reacts with methyl propiolate, methyl phenylpropiolate and methyl acetylpropiolate to give the
