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An enantioselective synthesis of carbafuranose sugars based on a linchpin carbacyclisation approach
- Source :
-
Tetrahedron: Asymmetry . May2009, Vol. 20 Issue 6-8, p821-831. 11p. - Publication Year :
- 2009
-
Abstract
- Abstract: Enantiopure carbafuranose derivatives were synthesised via a linchpin carbacyclisation process starting from 1,4-bisepoxides. Both 2-deoxy and 2-deoxy-6-hydroxycarbafuranose derivatives were obtained, which were converted to suitably protected precursors for carbanucleoside synthesis. [Copyright &y& Elsevier]
Details
- Language :
- English
- ISSN :
- 09574166
- Volume :
- 20
- Issue :
- 6-8
- Database :
- Academic Search Index
- Journal :
- Tetrahedron: Asymmetry
- Publication Type :
- Academic Journal
- Accession number :
- 39781265
- Full Text :
- https://doi.org/10.1016/j.tetasy.2009.02.019