An improved method for the synthesis of N-phenoxyacetylribonucleosides

Article abstract of DOI:10.1080/00397919508015877

N-phenoxyacetylribonucleosides were prepared efficiently from the reaction of ribonucleosides with phenoxyacetylchloride and 1,2,4-triazole (for adenosine and cytidine) or 1-hydroxybenzotriazole (for guanosine).

Full text of DOI:10.1080/00397919508015877

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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An Improved Method
for the Synthesis of N-
Phenoxyacetylribonucleosides
Kumud Kr. Singh b & P. Nahar a
a Ribozyme Research Laboratory Centre for
Biochemical Technology, Mall Road, Delhi, 110007,
India
b Department of Biophysics, University of Delhi,
South Campus Benito Juarez Road, Delhi, 110021,
India
Published online: 23 Sep 2006.
To cite this article: Kumud Kr. Singh & P. Nahar (1995) An Improved Method for
the Synthesis of N-Phenoxyacetylribonucleosides, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 25:13,
1997-2003, DOI: 10.1080/00397919508015877
To link to this article: http://dx.doi.org/10.1080/00397919508015877
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