Reactions of a-amino acids with ketones under hydrogenation conditions using 20% Pd(OH) 2 /C as the catalyst gave N-mono-alkylated amino acids in high yields. Reductive methylation of N-mono-alkylated amino acids under the same hydrogenation conditions at 50°C afforded N,N-di-alkylated amino acids i
A straightforward method for the simultaneous preparation of radiolabeled l-dihydroörotic and N-carbamyl-l-aspartic acids
✍ Scribed by Thomas W. Kensler; Nyun Han; David A. Cooney
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 380 KB
- Volume
- 111
- Category
- Article
- ISSN
- 0003-2697
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✦ Synopsis
A straightforward method is presented for the simultaneous enzymatic preparation of radiolabeled L-dihydroiirotic and N-carbamyl-L-aspartic acids. [carboxytT]Orotic acid is incubated in the presence of excess NADH to drive the reaction catalyzed by L-dihydroiirotate dehydrogenase in the reverse direction, forming L-[Y]dihydroLirotic acid. The contamination of the commercial reagent enzyme, L-dihydrohrotate dehydrogenase from Zymobacterium oroticum,
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