Synthesis of 3,6-Anhydro Sugars from Cyclic Sulfites and Sulfates and their Applications in the Preparation of Bicyclonucleoside Analogues of ddC and ddA
نویسندگان
چکیده
Absfract: Cyclic sulfates 21-23 and sulfite 27 derived from glucofuranose lead to the 3,6_anhydrosugar 28 in excellent yields when treated with sodium sulfite or in basic media. When treated with sodium sulfite, the 3-deoxy derivative 24 fails to give the intramolecular cyclization which leads to the anhydrosugars. Instead it gives the disulfonate derivative 26. 28 was used as starting material to prepare bicyclonucleosides 43 and 46, which are analogues of the anti-HIV agents ddC and ddA.
منابع مشابه
Pii: 0040-4039(94)85307-x
In carbohydrate chemistry, glycosylation remains the most difficult transformation to effect.’ Very few methods combine both high stereoselectivity and high yield in the formation of the glycosidic bond. Competing Gl and S$ processes often make it difficult to predict the stereochemical course of a neattion. In addition, many glycosylation conditions require the use of toxic heavy metal salts o...
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