Abstract
Both the (4S,5R)- and (4S,5S)-isomers of 4,5-dihydroxydecanoic acid ?-lactone, natural products and proposed autoregulators of Streptomyces Griseus, have been synthesised directly and in high yield from D-ribose via a common intermediate. © 1984.
| Original language | English |
|---|---|
| Pages (from-to) | 5215-5218 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 25 |
| Issue number | 45 |
| Publication status | Published - 1984 |
Fingerprint Dive into the research topics of 'The enantiospecific synthesis of (4S,5R)-and (4S,5S)-4,5-dihydroxydecanoic acid γ-lactones, proposed autoregulators from Streptomyces griseus'. Together they form a unique fingerprint.
Cite this
Cooper, R. D., Jigajinni, V. B., & Wightman, R. H. (1984). The enantiospecific synthesis of (4S,5R)-and (4S,5S)-4,5-dihydroxydecanoic acid γ-lactones, proposed autoregulators from Streptomyces griseus. Tetrahedron Letters, 25(45), 5215-5218.