## Abstract The title compounds were synthesized starting from dimethyl (2S,3aR,8aS)‐(+)‐8‐(phenylsulfonyl)hexahydrophyrrolo[2,3‐b]indole‐1,2‐dicarboxylate. This compound on treatment with LDA followed by reaction with [^14^C]methyl iodide or [^3^H]methyl iodide gave the methyl substituted derivati
Synthesis of [14C]-l-tryptophan and [14C]-5′-hydroxy-l-tryptophan labeled in the carboxyl group
✍ Scribed by E. Boroda; R. Kański; M. Kańska
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- French
- Weight
- 88 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.685
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✦ Synopsis
Abstract
The synthesis of selectively ^14^C‐labeled l‐tryptophan and its derivative 5‐hydroxy‐l‐tryptophan using chemical and multienzymatic methods is reported. The mixture containing [1‐^14^C[‐dl‐alanine, indole or 5‐hydroxyindole has been converted to [1‐^14^C]‐l‐tryptophan or 5′‐hydroxy‐[1‐^14^C]‐l‐tryptophan, respectively, in a one‐pot multienzymatic reaction using four enzymes: d‐amino acid oxidase, catalase, glutamic‐pyruvic transaminase and tryptophanase. Copyright © 2003 John Wiley & Sons, Ltd.
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