Pal, Chandan and Chakraborty, Tushar Kanti (2017) Synthesis of Amide-Linked Cyclic Dinucleotide Analogues with Pyrimidine Bases. In: ASIAN JOURNAL OF ORGANIC CHEMISTRY, 6 (10). pp. 1421-1427.
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Official URL: http://doi.org/10.1002/ajoc.201700260
Abstract
A convenient procedure has been developed for the synthesis of C-2-symmetrical cyclic dinucleotide analogues that contain all-pyrimidine bases (cytosine, uracil and thymine) with amide bonds in place of natural phosphodiester linkages, starting from commercially available d-glucose diacetonide (GDA). The Vorbruggen glycosylation of a common intermediate by using various pyrimidine bases was employed as the key step in the synthesis.
Item Type: | Journal Article |
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Publication: | ASIAN JOURNAL OF ORGANIC CHEMISTRY |
Additional Information: | Copy right for this article belongs to the WILEY-V C H VERLAG GMBH, POSTFACH 101161, 69451 WEINHEIM, GERMANY |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 11 Nov 2017 05:10 |
Last Modified: | 11 Nov 2017 05:10 |
URI: | http://eprints.iisc.ac.in/id/eprint/58207 |
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