Acyclic stereoselection. 28. Use of stereoselective aldol methodology in the total synthesis of cladinose.
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (8) , 1001-1004
- https://doi.org/10.1016/s0040-4039(00)98496-x
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Total synthesis of oleandrose and the avermectin disaccharide, benzyl .alpha.-L-oleandrosyl-.alpha.-L-4-acetoxyoleandrosideThe Journal of Organic Chemistry, 1983
- Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chlorideThe Journal of Organic Chemistry, 1978
- Hydroboration. XXXVI. Direct route to 9-borabicyclo[3.3.1]nonane via the cyclic hydroboration of 1,5-cyclooctadiene. 9-Borabicyclo[3.3.1]nonane as a uniquely selective reagent for the hydroboration of olefinsJournal of the American Chemical Society, 1974
- The synthesis of l-mycarose and l-cladinoseCanadian Journal of Chemistry, 1967
- The synthesis of L-()-mycarose and L-()-cladinoseTetrahedron, 1962
- Erythromycin. VII. The Structure of Cladinose1Journal of the American Chemical Society, 1956