Issue 3, 2008

Microwave-promoted efficient synthesis of C6-cyclo secondary amine substituted purine analogues in neat water

Abstract

The synthesis of C6-cyclo secondary amine-substituted purine analogues in neat water was achieved with the aid of microwave irradiation, providing a rapid, efficient and convenient method for the preparation of acyclic nucleosides in high yields.

Graphical abstract: Microwave-promoted efficient synthesis of C6-cyclo secondary amine substituted purine analogues in neat water

Supplementary files

Article information

Article type
Communication
Submitted
17 Dec 2007
Accepted
25 Jan 2008
First published
04 Feb 2008

Green Chem., 2008,10, 287-289

Microwave-promoted efficient synthesis of C6-cyclo secondary amine substituted purine analogues in neat water

G. Qu, L. Zhao, D. Wang, J. Wu and H. Guo, Green Chem., 2008, 10, 287 DOI: 10.1039/B719429C

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