79962-70-2Relevant academic research and scientific papers
NEW 1,3-DIPOLAR CYCLOADDITION LEADING TO 2,5-DIHYDROPYRROLE AND PYRROLIDINE DERIVATIVES
Achiwa, Kazuo,Sekiya, Minoru
, p. 1213 - 1216 (1981)
A novel 1,3-cycloaddition of intermediaries derived from N-(benzylidene)trimethylsilylmethylamine and acyl chlorides to conjugated olefins and acetylenes gave pyrrolidine and 2,5-dihydropyrrole derivatives, respectively.
1,3-Dipolar Cycloaddition Leading to N-Acylated Pyrrolidines and 2,5-Dihydropyrroles
Achiwa, Kazuo,Motoyama, Tadashi,Sekiya, Minoru
, p. 3939 - 3945 (2007/10/02)
Dipolar cycloaddition of an intermediary N-acyltrimethylsilylmethyliminium salt formed from N-(benzylidene)trimethylsilylmethylamine and acyl chloride to conjugated alkenes or alkines gave N-acylpyrrolidines or N-acyl-2,5-dihydropyrroles, respectively.The
