93066-50-3Relevant academic research and scientific papers
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions
Okoromoba, Otome E.,Li, Zhou,Robertson, Nicole,Mashuta, Mark S.,Couto, Uenifer R.,Tormena, Cláudio F.,Xu, Bo,Hammond, Gerald B.
, p. 13353 - 13356 (2016)
We developed an efficient fluorination protocol that converts easily accessible aziridines into β-fluoroamines, which are important motifs in biologically active molecules. In contrast with traditional fluorination approaches, DMPU-HF has shown both highe
[18F]Fluoroamines via ring-opening of N-Cbz-2-methylaziridine with [18F]-fluoride
Vasdev, Neil,van Oosten, Erik M.,Stephenson, Karin A.,Zadikian, Nonik,Yudin, Andrei K.,Lough, Alan J.,Houle, Sylvain,Wilson, Alan A.
body text, p. 544 - 547 (2009/04/14)
A highly regioselective method was developed for ring-opening benzyloxycarbonyl (Cbz)-protected 2-methylaziridine with [18F]-labelled fluoride. Following catalytic hydrogenation, 1-[18F]fluoro-2-propanamine ([18F]1) and 2-
L-aminodicarboxylic acid amides of alkoxyalkylamines
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, (2008/06/13)
The present invention is directed to new sweeteners of the formula: STR1 wherein, A is H, alkyl containing 1-3 carbon atoms, hydroxyalkyl containing 1-3 carbon atoms, alkoxymethyl wherein the alkoxy group contains 1-3 carbon atoms, or CO2 R in
L-aminodicarboxylic acid amides
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, (2008/06/13)
Amides of α-aminodicarboxylic acids and β-aminoethers are low calorie sweetners.
