1,3-Dipolar cycloaddition leading to N-alkylpyrrolidines.

1 January 1984

journal article
Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN

Vol. 32 (7) , 2878-2881
https://doi.org/10.1248/cpb.32.2878

Abstract

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

BENZYLIDENE
HALIDE
GIVE
METHYLENEIMINIUM
CONJUGATED
DIPOLAROPHILES
CYCLOADDITION LEADING
TRIMETHYLSILYLMETHYLAMINE