received in U.K. for publication 8 Iiovember 1971) 11-Desoxyproetaglandlna are of considerable current interest as possible substrates for mlcrobiological hydroxylatlon at C(ll) (pro&mold numbering) and elsewhere, as poaslble antagonlsta of the prostagl&dlns in the E and F series, and as hypotenslve
A simple and convenient route to 11-desoxyprostaglandins
โ Scribed by S. Ranganathan; D. Ranganathan; R. Iyengar
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- French
- Weight
- 271 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4020
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๐ SIMILAR VOLUMES
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In the preceding communication, we described an efficient coupling reaction of a,a'-dibromo ketones and furan. We demonstrate here that the adducts can readily be converted to troponoid compounds.
The intensity of the two lines at 25 MHz remained constant over the concentration range investigated, and, since the maximum line separation is ca. 0.4 MHz, that is the magnetic environment of the two protons is very similar, significantly different relaxation effects are highly improbable. For thes