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An investigation into the catalytic deuteration and tritiation of dehydroproline9-buserelin

✍ Scribed by J. Oehlke; T. Brankoff; M. Schmidt; M. Brudel; U. Kertscher; H. Berger


Publisher
John Wiley and Sons
Year
1993
Tongue
French
Weight
439 KB
Volume
33
Category
Article
ISSN
0022-2135

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✦ Synopsis


Abstract

For optimizing the catalytic tritiation of peptides, the catalytic deuteration of buserelin and DhP^9^‐buserelin^1^ in DMA after reaction of DhP^9^‐buserelin were comparable in both solvents. The nonspecific incorporation of deuterium found after deuteration of buserelin was clearly lower after reaction in DMA. Tritiation of DhP^9^‐buserelin in DMA using 85% tritium gas, with conditions optimized by the deuteration experiments, resulted in a specific radioactivity of 1.3 TBq/mmol. 72 and 13 percent of the incorporated radioactivity were found to be associated with proline and histidine, respectively, after acidic hydrolysis.


πŸ“œ SIMILAR VOLUMES


Investigation of the catalytic deuterati
✍ J. Oehlke; H. Niedrich; H.-J. ZΓΆpfl; P. Franke πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 French βš– 287 KB

As a model for the tritium labelling of peptides the catalytic deuteration of N-acetyl-OL-3,4-dehydroproline amide was investigated by means of mass spectrometric measurements. The unwanted incorporation of hydrogen instead of deuterium, found especially in the presence of water, was compensated par

Investigation on solvent hydrogen transf
✍ J. Oehlke; H. Niedrich; H.-J. ZΓΆpfl; P. Franke πŸ“‚ Article πŸ“… 1989 πŸ› John Wiley and Sons 🌐 French βš– 319 KB

amide solvent hydrogen was incorporated instead of deuterium up to an order of 70%. The major part of the solvent hydrogen was shown to be introduced into the reaction product independently of the dilution of the reacting gas. This direct transfer depends on type of solvent and catalyst and on the c