Studies in macrolide synthesis: A stereocontrolled synthesis of a (9S)-macrolide intermediate for oleandomycin using chiral boron reagents.
- 24 March 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (13) , 1767-1770
- https://doi.org/10.1016/s0040-4039(00)91728-3
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
- Total synthesis of the macrolide antibiotic cytovaricinJournal of the American Chemical Society, 1990
- Enantio- and diastereoselective aldol reactions of achiral ethyl and methyl ketones with aldehydes: the use of enol diisopinocampheylborinatesTetrahedron, 1990
- Aldol reactions of methylketones using chiral boron reagents: A reversal in aldehyde enantioface selectivityTetrahedron Letters, 1989
- Studies in macrolide synthesis: A highly stereoselective synthesis of (+)-(9S)-dihydroerythronolide a using macrocyclic stereocontrolTetrahedron Letters, 1989
- Studies in macrolide synthesis: A concise asymmetric synthesis of a macrolide intermediate for the erythronolides.Tetrahedron Letters, 1988
- Aldol condensations of chiral ethylketones: Control by chiral boron reagents.Tetrahedron Letters, 1988
- Enantioselective aldol condensations: The use of ketone boron enolates with chiral ligands attached to boron.Tetrahedron Letters, 1986
- Tetrahedron report number 190Tetrahedron, 1985
- Synthesis of tylonolide, the aglycone of tylosinJournal of the American Chemical Society, 1982
- Total synthesis of 6-deoxyerythronolide BJournal of the American Chemical Society, 1981