Synthetic studies on palytoxin stereocontrolled practical synthesis of the C.85 – C.98 segment
- 31 December 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (22) , 2243-2246
- https://doi.org/10.1016/s0040-4039(00)81894-8
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Stereochemistry of palytoxin. Part 4. Complete structureJournal of the American Chemical Society, 1982
- Highly stereoselective approaches to .alpha.- and .beta.-C-glycopyranosidesJournal of the American Chemical Society, 1982
- Absolute stereochemistry of palytoxinJournal of the American Chemical Society, 1982
- Regio- and stereoselective ring opening of epoxy alcohols with organoaluminium compounds leading to 1,2-diolsTetrahedron Letters, 1982
- Structure of palytoxinJournal of the American Chemical Society, 1981
- Further synthetic studies on rifamycin sTetrahedron, 1981
- Further studies on palytoxin. II. structure of palytoxinTetrahedron Letters, 1981
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980
- Stereo- and regioselective methods for the synthesis of three consecutive asymmetric units found in many natural productsTetrahedron Letters, 1979
- Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chlorideThe Journal of Organic Chemistry, 1978