94191-22-7Relevant articles and documents
[3+2] Cycloadditions and nucleophilic additions of aziridines under C-C and C-N bond cleavage
Gaebert, Garsten,Mattay, Jochen
, p. 14297 - 14316 (2007/10/03)
Under PET conditions (photoinduced electron transfer) aziridines react with dipolarophiles in a [3+2] cycloaddition to form five-membered heterocycles. In this study we used mono- and disubstituted N-alkyl and N-arylaziridines. We noticed that the radical
1,3-DIPOLAR CYCLOADDITION LEADING TO N-ALKYLPYRROLIDINES
Achiwa, Kazuo,Imai, Nobuyuki,Inaoka, Tetsuya,Sekiya, Minoru
, p. 2878 - 2881 (2007/10/02)
1,3-Dipolar cycloaddition of an intermediary methyleneiminium ylide formed from N-(benzylidene)trimethylsilylmethylamine and alkyl halide to conjugated olefinic dipolarophiles has been found to give N-alkylpyrrolidines.KEYWORDS - N-alkylpyrrolidine; N-unsubstituted pyrrolidine; 1,3-dipolar cycloaddition; N-alkyltrimethylsilylmethyliminium salt; methyleneiminium ylide