## Abstract An enzymatic synthesis of [^11^C]__N__‐acetyl‐D‐glucosamine is described. ^11^CO~2~ is reacted with methylmagnesium bromide to form [1‐^11^C]acetate. The latter is converted to [^11^C]acetylcoenzyme A by passage over an enzyme reactor containing immobilized acetylcoenzyme A synthetase (
One-Day Enzymatic Synthesis and Purification of UDP–N- [1-14C]Acetyl-Glucosamine
✍ Scribed by Barbara Leiting; KellyAnn D. Pryor; Suzanne S. Eveland; Matt S. Anderson
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 104 KB
- Volume
- 256
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A method for the enzymatic synthesis of [1-14 C-N-acetyl, P 18 O 2 ] cytidine monophosphate neuraminic acid (CMP-NeuAc) is described. Central to the synthesis of [1-14 C-N-acetyl, P 18 O 2 ]CMP-NeuAc was the enzymatic preparation of [g-P 18 O 3 ]ATP for use in a reaction with uridine kinase and cyti
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
UDP-3-O-(R-3-hydroxydecanoyl)-N-[ 3 H-acetyl]glucosamine, was prepared using a modified procedure for the preparation of carboxamides reported by Kunishima et al. using [ 3 H]CH 3 CO 2 Na, 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride, N-methylmorpholine and UDP-3-O-(R-3-hydroxy