Efficient and selective synthesis of glycofuranosyl azides and nucleosides from cyclic 1,2-thiocarbonate sugars.
نویسندگان
چکیده
[reaction: see text] Cyclic 1,2-thiocarbonate sugars are convenient starting materials for the selective and efficient preparation of glycofuranosyl azides and nucleosides by regio- and stereoselective thiocarbonate ring-opening.
منابع مشابه
Highly b-stereoselective nucleosidation from a-D-xylo- and a-D-ribo-furanose 1,2-thiocarbonates
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عنوان ژورنال:
- Organic letters
دوره 5 15 شماره
صفحات -
تاریخ انتشار 2003