Regioselective syntheses of 5- and 6-aminoanthracene-2,3-dimethanol
โ Scribed by Shusen Sun; John Desper
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 695 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Three phenolic derivatives of 2-aminoanthracene have been prepared as their diacetyl derivatives by Bucherer-type amination of appropriately substituted anthracenes. Since many aromatic compounds are metabolized to phenolic products' in mammalian systems by oxygenases such as cytochrome P-450, the n
Convenient syntheses of 2,4-,a,a-and 5,B-deuterium labelled 6-hydroxydopamines have been developed. 2,4,5-Trimethoxybenzaldehyde (1) was reductively aminated to give 2,4,5-trimethoxybenzylamine (2). Quaternization of the amine with methyliodide followed by displacement with cyanide gave 2,4,5-trimet
The intramolecular addition of hydroxyl group of 3-(3-hydroxyl)propylidene-2,5\_piperazinedione to 3-position and the same substitution of 3-(3-hydroxy)propyl derivative to 6-position gave the corresponding 3-spiro-and 3,6bridged 2,5\_piperazinediones, respectively. Recently, much attention is bein
## Abstract For Abstract see ChemInform Abstract in Full Text.