82959-82-8Relevant articles and documents
One-Pot Synthesis of N-Alkylpyrrolidines by 1,3-Dipolar Cycloaddition
Imai, Nobuyuki,Achiwa, Kazuo
, p. 593 - 601 (2007/10/02)
N-Alkylpyrrolidines were obtained by one-pot synthesis through 1,3-dipolar cycloaddition of the N-alkylazomethine ylide intermediates generated from N-(benzylidene)trimethylsilylmethylamine and alkyl halide or tosylate.
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
WATER-INDUCED FORMATION OF AZOMETHINE YLIDE 1,3-DIPOLE. STEREOSPECIFIC AND REGIOSELECTIVE CYCLOADDITION REACTIONS
Tsuge, Otohiko,Kanemasa, Shuji,Hatada, Akira,Matsuda, Koyo
, p. 801 - 804 (2007/10/02)
An N-(trimethylsilylmethyl)imine generates the azomethine ylide 1,3-dipole of nonstabilized type, when treated with water, which cycloadds to olefinic dipolarophiles in a stereospecific and regioselective manner.