Colorimetric Determination of O,O-dimethy(1-hydroxy-2,2,2-trichloroethyl)phosphonate and Its Higher Homologs
β Scribed by Mustafa, Ahmed; Sidky, M. M.; El-Darawy, Z. I.; Kamel, Hussein
- Book ID
- 126844194
- Publisher
- American Chemical Society
- Year
- 1966
- Tongue
- English
- Weight
- 348 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0021-8561
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The total synthesis of 1-O-alkyl-2-acetyl-3-glyceryl-(2-trimethyl ammoniummethyl)phosphonate, the phosphono analogue of 1-O-alkyl-2-acetyl-sn-glyceryl-3-phosphorylcho~ne, is described. The phosphonolipid shows much lower activity than the phospholipid stimulating serotonin release from rabbit platel
Treatment of benzyl O-/?-n-galactopyranosyl-( 1+3)-2-acetamido-2-deoxy-4,6-O-isopropylidene-j3-D-glucopyranoside with tert-butylchlorodiphenylsiiane afforded the 6'-0-tert-butyldiphenylsilyl ether, which was converted into the 3',4'-0-isopropylidene derivative. Methylation and subsequent removal of
In a study designed to explore the physical chemical characteristics of platelet activating factor (PAF), or 1-O-alkyl-2-acetyl-sn-glycero-3-phosphocholine, the critical miceUar concentration of this compound, as well as the propionyl, butyryl and hexanoyl homologs was determined. In addition, an an