79962-72-4Relevant articles and documents
Trimethylsilyl Triflate-Catalyzed 1,3-Dipolar Cycloaddition Leading to N-Unsubstituted Pyrrolidines
Achiwa, Kazuo,Sugiyama, Kaori,Sekiya, Minoru
, p. 1975 - 1981 (2007/10/02)
Dipolar cycloaddition of an intermediary N-trimethylsilyltrimethylsilylmethyliminium salt formed from N-(benzylidene)trimethylsilylmethylamine by the catalytical action of trimethylsilyl triflate to conjugated alkene or alkyne gave N-unsubstituted pyrroli
NEW 1,3-DIPOLAR CYCLOADDITION LEADING TO 2,5-DIHYDROPYRROLE AND PYRROLIDINE DERIVATIVES
Achiwa, Kazuo,Sekiya, Minoru
, p. 1213 - 1216 (2007/10/02)
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.