## Abstract Shikimic‐6‐^13^C acid, 43 ± 5% enriched, was synthesized from 91% enriched acetic‐2‐^13^C acid via 91% enriched phosphoenolpyruvic‐3‐^13^c acid. The latter intermediate was condensed with erythrose‐4‐phosphate by a cell free extract of __E__. __coli__ 83‐24.
Synthesis of D-(-)-[1,7-13C2]shikimic acid
✍ Scribed by Hyeongjin Cho; Lutz Heide; Heinz G. Floss
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- French
- Weight
- 255 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
The chemical synthesis of 99% enriched D(‐)‐[1,7‐^13^C~2~]shikimic acid from [1,2‐^13^C~2~]acetate in 25% overall yield is described. A two‐carbon phosphonate synthon was prepared from [1,2‐^13^C~2~]acetate and used in the shikimate synthesis of Fleet and coworkers.
📜 SIMILAR VOLUMES
## Abstract The synthesis of (1,2‐ ^13^C~2~) 2‐phosphoglycelic acid, 5, from commercially‐available (1,2‐ ^13^C~2~) bromoacetic acid is described along with some of its solution NMR characteristics.
Enantiospecific Synthesis of (-)-5-epi-Shikimic Acid and (-)-Shikimic Acid. -The key step in the synthesis of the title compounds (XI) and (XVI) is the intramolecular cycloaddition of the nitrones (V) and (XIV). -