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Tritium-labelling of Natural Products

✍ Scribed by MAURER, RAINER; WENZEL, MARTIN; KARLSON, PETER


Book ID
109635872
Publisher
Nature Publishing Group
Year
1964
Tongue
English
Weight
343 KB
Volume
202
Category
Article
ISSN
0028-0836

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πŸ“œ SIMILAR VOLUMES


Tritium-labelling of lipids
✍ V. P. Shevchenko; N. F. Myasoedov πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 French βš– 562 KB

## Abstract Tritium‐labelled lipid preparations are obtained by heterogeneous isotopic exchange with gaseous tritium in solution. After appropriate purification, the localization of the label was determined in the main fragments of [^3^H]‐compounds. The obtained data on specific radioactivity and t

Tritium labelling of nitroaryldihydropyr
✍ Ulrich Pleiß; Peter Schmitt πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 French βš– 173 KB

## Abstract The synthesis of tritium labelled nitroaryldihydropyridines was achieved by dehalogenation of a brominated precursor using the palladium hydroxide on charcoal as catalyst. The investigations described show the example [^3^H]nimodipine which was prepared with a specific activity of 16,4

Tritium labelling of polyols
✍ G. P. Akulov; E. V. Snetkova; Ju. L. Kaminski; B. K. Kudelin; V. L. Efimova πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 French βš– 122 KB

## Abstract Mannitol, galactitol and myo‐inositol were labelled by a solid state isotope exchange with gaseous tritium. The labelled polyois were prepared with specific activities in the range 740–4440 TBq/mol (20–120 kCi/mol) after purification by HPLC.

Tritium Labelling of Antibodies
✍ ROSΓ‰N, C.-G.; EHRENBERG, L.; AHNSTRΓ–M, G. πŸ“‚ Article πŸ“… 1964 πŸ› Nature Publishing Group 🌐 English βš– 286 KB
Tritium labelling of psychopharmacologic
✍ Ouri Buchman; Michael Shimoni πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 French βš– 362 KB

## Abstract Attempts to reach phenothiazine derivatives labelled with tritium at high specific activity, are described. All the syntheses are based on catalysed dehalogenation procedures. The most encouraging results are those obtained by halogenation of the desired compound followed by catalytic d