Stereocontrolled synthesis of chiral synthons for polyketide-derived natural products
- 1 January 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (19) , 1987-1990
- https://doi.org/10.1016/s0040-4039(00)81823-7
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Specific removal of o-methoxybenzyl protection by DDQ oxidation.Tetrahedron Letters, 1982
- Further synthetic studies on rifamycin sTetrahedron, 1981
- Asymmetric epoxidation provides shortest routes to four chiral epoxy alcohols which are key intermediates in syntheses of methymycin, erythromycin, leukotriene C-1, and disparlureJournal of the American Chemical Society, 1981
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980
- Chiral synthons for the total synthesis of macrolide antibioticsJournal of the Chemical Society, Chemical Communications, 1980
- Stereo- and regioselective methods for the synthesis of three consecutive asymmetric units found in many natural productsTetrahedron Letters, 1979
- Branched-chain sugar nucleosides. IV. 9-(3-Deoxy-3-C-"hydroxymethyl"-β(and α)-D-allofuranosyl and ribofuranosyl)adenineCanadian Journal of Chemistry, 1969
- Branched-chain sugar nucleosides. III. 9-(3-Deoxy-3-C-methyl-β-D-allofuranosyl and ribofuranosyl)adenineCanadian Journal of Chemistry, 1969