4.2 Article

Multicomponent solvent-free cyclocondensation/glycosylation strategy for thiazolo-s-triazine N-nucleosides

Journal

LETTERS IN ORGANIC CHEMISTRY
Volume 4, Issue 1, Pages 47-50

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/157017807780037469

Keywords

multicomponent reactions; solvent-free; glycosylation; microwaves; thiazolo-s-triazines; pyrano N-nucleosides

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A green protocol involving novel three-component one-pot cyclocondensation reactions of 2-amino-4-aryl-thiazoles, aromatic aldehydes and ammonium thiocyanate under solvent-free microwave irradiation (MWI) conditions expeditiously yields thiazolo-s-triazine nucleobases, which afford the corresponding pyrano N-nucleosides on I-2 promoted glycosylation with 1,2,3,4-tetra-O-acetyl-beta-D-ribo/xylopyranose under MWI followed by deacetylation.

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