An Enantioselective Synthesis of a Macrolide from the Polyketide Lactone Derived from Oleandomycin
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference12 articles.
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2. THE STRUCTURE OF OLEANDOMYCIN
3. 8, 8A-DEOXYOLEANDOLIDE: ELABORATED BY A BLOCKED MUTANT OF THE ERYTHROMYCIN-PRODUCING ORGANISM STREPTOMYCES ERYTHREUS
4. Peptide SynthesisviaOxidation-Reduction Condensation by the Use of Non-metallic Compound as a Mercaptan Scavenger
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1. Synthesis, Conformational Analysis, and Stereoselective Reduction of 14-Membered Ring 3-Keto Lactones;The Journal of Organic Chemistry;1994-12
2. Synthetic studies on naphthopyrans from a polyketide lactone;Tetrahedron Letters;1993-07
3. Synthesis and characterization of a 14-membered polyketide lactone;Tetrahedron Letters;1993-07
4. Stereoselective Synthesis of the C-8–C-13 Segment of Oleandonolide;Mendeleev Communications;1991-01
5. Biosynthetic studies on oleandomycin by incorporation of the chemically synthesized aglycones.;The Journal of Antibiotics;1990
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