Solid-Liquid Phase Transfer Catalytic Synthesis(VI) 1:3-Dipolar Cycloaddition Reactions of Aldimines

1 January 1987

journal article
research article
Published by Taylor & Francis in Synthetic Communications

Vol. 17 (1) , 33-38
https://doi.org/10.1080/00397918708063901

Abstract

1:3-Dipolar cycloaddition reactions of aldimines with dipolarophiles can be performed under solid-liquid phase transfer catalytic conditions or in protic alkanol solvents using solid K₂CO₃ as a base. The reactions are synthetically useful in preparing NH-pyrrolidines.

Keywords

CYCLOADDITION REACTIONS
DIPOLAR CYCLOADDITION
SOLID LIQUID
CATALYTIC SYNTHESIS
TRANSFER CATALYTIC
ALDIMINES
LIQUID PHASE TRANSFER

This publication has 1 reference indexed in Scilit:

Alkylation and Michael additions of glycine ethyl ester. Use in .alpha.-amino acid synthesis and as acyl carbanion equivalent
The Journal of Organic Chemistry, 1976