Published in

Thieme Gruppe, Synlett: Accounts and Rapid Communications in Synthetic Organic Chemistry, 11(2010), p. 1669-1673, 2010

DOI: 10.1055/s-0030-1258082

Links

Tools

Export citation

Search in Google Scholar

A Facile Synthesis of Novel Pyrrolidine Dendrimers by Terminal Group Modification through 1,3-Dipolar Cycloaddition Reaction

Journal article published in 2010 by Perumal Rajakumar, Sebastian Raja ORCID, Ayyavu Thirunarayanan, Thiru Narayanan
This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Red circle
Preprint: archiving forbidden
Orange circle
Postprint: archiving restricted
Upload
Red circle
Published version: archiving forbidden
Policy details
Data provided by SHERPA/RoMEO

Abstract

A series of novel dendrimers with pyrrolidine as surface group has been achieved in high yields by terminal-group modification on chalcone dendrimers through the application of 1,3-dipolar cycloaddition reaction. In 1,3-dipolar cycloaddition, azomethine ylides (AMY) with alkenes afforded five-membered N-methyl pyrrolidine. The formation of N-methyl pyrrolidine in the dendritic structure would be