Synthetic studies relating to the C1–C9 “Eastern” Half of Rosaramicin
- 1 January 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (44) , 5335-5338
- https://doi.org/10.1016/s0040-4039(00)85204-1
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Total synthesis of (+)-rosaramicin aglycone and its diacetate.Journal of the American Chemical Society, 1986
- Macrocyclic stereocontrol. Total synthesis of (.+-.)-3-deoxyrosaranolideJournal of the American Chemical Society, 1984
- New strategy for carbohydrate-based syntheses of multichiral arrays: pyranosidic homologation. 2Journal of the American Chemical Society, 1984
- REACTION OF 2,3-ANHYDR0-4,6-O-BENZYLIDENE-α-d-HEXOPYRANOSIDES WITH PROPENYLMAGNESIUM CHLORIDES. REGIOSELECTIVE CARBON CHAIN EXTENSION AT THE C-2 POSITION OF HEXOPYRANOSIDESChemistry Letters, 1983
- Revision of the assignment of relative stereochemistry in sibirosamine: synthesis of methyl n-tosyl α-d-disirosaminopyranosideTetrahedron Letters, 1982
- Chemical degradation and X-ray crystal structure of rosaramicinTetrahedron Letters, 1980
- X-ray crystallography of protylonolide and absolute configuration of tylosin.The Journal of Antibiotics, 1980
- Chemical and biological studies on 16-membered macrolide antibiotics.The Journal of Antibiotics, 1975
- The chemistry of the leucomycins. I. Partial structure of leucomycin A3Tetrahedron Letters, 1967