## Abstract Methyl iodide ^14^C is reacted with lithium p‐methoxy phenylacetylenide to give with a 85% yield 1‐p‐methoxy‐phenyl‐1‐propyne‐3‐^14^C. Reduction of the latter with LiAlH~4~ leads to a mixture of trans anethole‐3‐^14^C (85%) and cis anethole (15%) with a 55% yield. After preparative gas
Preparation Microbiologique Du 2-CETO-3-Desoxy-D-Gluconate 1-14C ou U-14C
✍ Scribed by J. Pouyssegur
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- French
- Weight
- 358 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A E. Coli K 12 mutant having lost 2‐keto‐3‐desoxy‐gluconate kinase activity is unable to utilize glucuronate as a unique carbon source. However, this strain is able to partially convert glucuronate into KDG in resting cells conditions reported here.
A method is described making it possible to produce 1‐ ^14^C‐KDG or U‐^14^C‐KDG when the kinase cells metabolise 6‐^14^C or U‐^14^C‐D‐glucuronate. The radioactive KDG accumulated in the incubation medium has been purified thanks to a biological specific method followed by chromatography on anionic resin. The yield of the purified KDG from the hexuronate is about 20%. According to chromatographic criteria and specific conversion by KDG‐kinase, the product obtained has been authenticated as true KDG.
📜 SIMILAR VOLUMES
## Abstract Methyl cinnamate ‐3‐^14^C is reduced smoothly in excellent yield to cinnamyl alcohol ‐3‐^14^C by aluminum hydride. without attack of the double bond. After purification by column chromatography cinnamyl alcohol ‐3‐^14^C is obtained with a radioactive overall yield of 65% based on cinnam
The ^14^C labelling of three compounds : HI‐6, TMB‐4 and pyrimidoxime is described from ^14^C‐formic acid, sodium salt. The compounds were prepared by lithiation and formylation with N‐methyl (^14^C)‐formanilide followed by introduction of the hydroxylamine moieties and alkylation of the pyridine. R
A notre connaissance, il ne a m b l e pas que le Dsannose-1-phosphate radioactif, marque au carbone m u le mannose, puisse 8tre obtenu aisement suprbs den centres de preparation de mol6culea msrqu8ea. Cet ester phosphorique presentant un interat pour l'etude de differentee enzymes du mBtabolisme du
## Abstract The synthesis of 1,2,3,4,6‐penta‐__O__‐galloyl‐[U‐^14^C]‐D‐glucopyranose is described. [U‐^14^C] glucopyranose was reacted with tri‐O‐benzylgallic acid forming 1,2,3,4,6‐penta(tri‐O‐benzylgalloyl)‐[U‐^14^C]‐D‐glucopyranose as chromatograpically separable anomers. Removal of the benzyl g