Novel convenient synthesis of biologically active esters of hydroxylamine
β Scribed by Maxim A. Khomutov; Swati Mandal; Janne Weisell; Neiha Saxena; Alina R. Simonian; Jouko Vepsalainen; Rentala Madhubala; Sergey N. Kochetkov
- Book ID
- 106221958
- Publisher
- Springer
- Year
- 2009
- Tongue
- English
- Weight
- 311 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0939-4451
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The high reactivity of the phosphonofommte mo~y requires development of a novel synthesis for esters of phosphonoformate, which is reported together with preliminary data on the antiviral activity of these esters.
The oxidation of a range of b-cyanoethyl tertiary amines with mCPBA gives the corresponding N-oxides, which can be isolated or undergo Cope-elimination to give secondary hydroxylamines in excellent yield.
Vitamin A derivatives / Retinoic acid derivatives / Tumor inhibitors / Koenigs-Knorr reaction / Glucuronides The toxic and teratogenic effects caused by the highly biolo-synthesized under Koenigs-Knorr conditions from (all-E)-retigically active (all-E)-retinoic acid and its derivatives n&l and an a