The enantiospecific synthesis of (4S,5R)-and (4S,5S)-4,5-dihydroxydecanoic acid γ-lactones, proposed autoregulators from Streptomyces griseus
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (45), 5215-5218
- https://doi.org/10.1016/s0040-4039(01)81567-7
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Carbon-carbon bond formation using primary tosylates derived from carbohydratesTetrahedron Letters, 1984
- Synthesis of (4s,5r)-(+)-factor, a proposed autoregulator of anthracycline biosynthesisTetrahedron, 1984
- On the biological inactivity of 4,5-dihydroxy-n-decanoic acid-4-lactones.The Journal of Antibiotics, 1983
- Synthesis of saccharides and related polyhydroxylated natural products. 3. Efficient conversion of 2,3-erythro-aldoses to 2,3-threo-aldosesJournal of the American Chemical Society, 1982
- Isolation and structure of novel autoregulators from Streptomyces griseus.The Journal of Antibiotics, 1982
- Synthesis and absolute configuration of A-factor, the inducer of streptomycin biosynthesis in inactive mutants ofTetrahedron Letters, 1981
- New isopropylidene derivatives of d-ribose: 1,2:3,4-di-O-isopropylidene-d-ribopyranose and 1,2-O-isopropylidene-d-ribopyranoseCarbohydrate Research, 1965