Synthesis of spiroacetal-nucleosides as privileged natural product-like scaffolds.
نویسندگان
چکیده
The elaboration of a 6,6-spiroacetal scaffold to incorporate a nucleoside unit at the anomeric position is described. The novel spiroacetal-nucleoside hybrids were generated via nucleosidation of acetoxy-spiroacetal with a series of silylated nucleobases under Vorbrüggen conditions.
منابع مشابه
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عنوان ژورنال:
- Organic & biomolecular chemistry
دوره 7 7 شماره
صفحات -
تاریخ انتشار 2009