Formation of phostonic acids during the reduction of azidonucleosidephosphonic acids
β Scribed by Michael Morr; Christel Kakoschke; Ludger Ernst
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 204 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Reduction of 5%-azido-3%,5%-dideoxy-3%-(phosphorylmethyl)nucleosides, either with H 2 /Pd/C or with dithiothreitol, leads to cyclic phosphonate esters (phostonic acids) in addition to the desired 5%-amino compounds. The phostonic acids are obtained as the main products when a 20-fold excess of dithiothreitol is used.
π SIMILAR VOLUMES
The stoichiometry of formation and the kinetics of reduction of molybdothorophosphoric acid in nitric acid solutions were studied spectrophotometrically. The Mo:Th:P ratio in the complex is 12:1:1, assuming that Mo(VI) exists in acid solutions as a dimer. The ternary heteropoly acid is more stable a
## ABSTRAa Careful hydrolysis of (+ kis-or (+ )-trans-tetrahydro-2,5-dimethoxy-2-furaldehyde dimethyl acetal proceeded via 5,5-dimethoxy-4-oxopentanal to give (+ )-tram-4-hydroxy-5-methoxy-2-cyclopentenone and ( f )-rrans-4,5-dihydroxy-2qclopentenone. The latter product did not isomerize to 2,3-d