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Issue 3, 2008
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Microwave-promoted efficient synthesis of C6-cyclo secondary amine substituted purine analogues in neat water

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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

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Publication details

The article was received on 17 Dec 2007, accepted on 25 Jan 2008 and first published on 04 Feb 2008


Article type: Communication
DOI: 10.1039/B719429C
Citation: Green Chem., 2008,10, 287-289
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    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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