1,3-DIOXAN-5-ONE AS C-3-BUILDING BLOCK FOR THE DIASTEREOSELECTIVE ANDENANTIOSELECTIVE SYNTHESIS OF C-5-DEOXY TO C-9-DEOXY SUGARS USING THESAMP-HYDRAZONE RAMP-HYDRAZONE METHOD

Authors
ENDERS D JEGELKA U
Citation
D. Enders et U. Jegelka, 1,3-DIOXAN-5-ONE AS C-3-BUILDING BLOCK FOR THE DIASTEREOSELECTIVE ANDENANTIOSELECTIVE SYNTHESIS OF C-5-DEOXY TO C-9-DEOXY SUGARS USING THESAMP-HYDRAZONE RAMP-HYDRAZONE METHOD, Tetrahedron letters, 34(15), 1993, pp. 2453-2456
Citations number
29
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
15
Year of publication
1993
Pages
2453 - 2456
Database
ISI
SICI code
0040-4039(1993)34:15<2453:1ACBFT>2.0.ZU;2-7
Abstract
The diastereo- and enantioselective synthesis of deoxy- and, dideoxysu gars is demonstrated using the protected dihydroxyacetone derivative 8 as a C3-building block in combination with the SAMP-/RAMP-hydrazone m ethod.