Reaction of Alanine Racemase with 1-Aminoethylphosphonic Acid Forms a Stable External Aldimine
✍ Scribed by Stamper, Geoffrey, F.; Morollo, Anthony A.; Ringe, Dagmar
- Book ID
- 125974556
- Publisher
- American Chemical Society
- Year
- 1999
- Tongue
- English
- Weight
- 4 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0006-2960
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract 2‐Aminoethylphosphonic acid and fosfomycin produced on feeding D‐[1‐^2^H~1~]glucose to __Tetrahymena thermophila__ and __Streptomyces fradiae__, respectively, indicate that the phosphoenolpyruvate mutase catalyzes the stereospecific transfer of the phospho group of (__Z__)‐phosphoenol‐[
A new type of Lewis acid, scandium trisdodecylsulfate (STDS), was prepared. In the presence of a catalytic amount of STDS, aldol reactions of silyl enol ethers with aldehydes proceeded smoothly in water without using any organic solvents. It was proven that stable dispersion systems including the ca
The reaction of C02 with GRIGNARD reagents carrying an ether grouping in a sterically suitable position can be directed to afford predominantly either the carboxylic acid or the symmetrical ketone. Thus, the magnesiumorqanic compounds prepared from chloromethyl-methyl ether, benzyl-chloromethyl ethe