Campus Units

Chemistry

Document Type

Article

Publication Version

Published Version

Publication Date

2-2005

Journal or Book Title

Organic Letters

Volume

7

Issue

6

First Page

1035

Last Page

1037

DOI

10.1021/ol047468h

Abstract

Several water-soluble calix[4]arenes were synthesized via Huisgen 1,3-dipolar cycloaddition between azides and alkynes. Cationic, anionic, and nonionic calixarenes were prepared from a common azidocalixarene intermediate. Azidocalixarenes performed better than alkynylcalixarenes as precursors. The aggregation behavior of the water-soluble calixarenes was studied by 1H NMR spectroscopy.

Comments

Reprinted (adapted) with permission from Organic Letters (2005): 1-35, doi:10.1021/ol047468h. Copyright 2005 American Chemical Society.

Copyright Owner

American Chemical Society

Language

en

File Format

application/pdf

Included in

Chemistry Commons

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