Reductive rearrangement of 2,3-unsaturated methyl pyranosides to 3-deoxy glycals
- 31 December 1972
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 13 (13) , 1205-1208
- https://doi.org/10.1016/s0040-4039(01)84548-2
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Specifically 2-monodeuterated 2-deoxy-D-riboses (2(S)- and 2(R)-deuterio-2-deoxy-D-erythropentoses)Journal of the American Chemical Society, 1971
- Synthesis of methyl 2,3-dideoxy-DL-alk-2-enopyranosides from furan compoundsTetrahedron, 1971
- Route to 3-deoxy glycals via an abnormal lithium aluminum hydride reductive rearrangement of some unsaturated acetalsJournal of the American Chemical Society, 1970
- Conformations. VI. Vinyl-Allylic Proton Spin CouplingsJournal of the American Chemical Society, 1964