A cyclodextrin molecular reactor for the regioselective synthesis of 1,5-disubstituted-1,2,3-triazoles

Date

2005

Authors

Barr, Lorna
Lincoln, Stephen F
Easton, Christopher

Journal Title

Journal ISSN

Volume Title

Publisher

Taylor & Francis Group

Abstract

6A-Deoxy-6A-propynamido-β-cyclodextrin reacts with 4-tert-butylphenyl azide in aqueous solution, to form the 5-(aminocarbonyl)-substituted triazole in preference to the 4-(aminocarbonyl)- substituted analogue, in a ratio of 25:1. The cyclodextrin moiety

Description

Keywords

Keywords: Cycloadditions; Cyclodextrins; Molecular reactors; Regio selectivity; Templates; Triazoles

Citation

Source

Supramolecular Chemistry

Type

Journal article

Book Title

Entity type

Access Statement

License Rights

Restricted until

2037-12-31