Controlled Acetolysis of 3,6-Anhydro-5-o-benzyl-1,2-o-isopropylidene-α-d-glucofuranose: Synthesis of 1-(3′,6′-Anhydro- α-d-glucofuranosyl)thymine
Author:
Affiliation:
1. a Organic Chemistry Division III , Indian Institute of Chemical Technology , Hyderabad, India
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1081/SCC-120021846
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1. Potential Anticancer Agents.1 XV. Synthesis of 9-β-D-Glucofuranosyladenine
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3. Total synthesis of griseolic acid derivatives from D-glucose
4. Synthesis of novel 3′,6′-dideoxy-3′,6′-epithio and 2′,6′-dideoxy-2′,6′-epithio nucleosides
5. Nucleosides. 116. 1-(.beta.-D-Xylofuranosyl)-5-fluorocytosines with a leaving group on the 3' position. Potential double-barreled masked precursors of anticancer nucleosides
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3. Controlled Acetolysis of 3,6-Anhydro-5-o-benzyl-1,2-o-isopropylidene-α-D-glucofuranose: Synthesis of 1-(3′,6′-Anhydro-α-D-glucofuranosyl)thymine.;ChemInform;2003-11-18
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