94191-30-7Relevant academic research and scientific papers
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.
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
