53866-33-4Relevant academic research and scientific papers
Shifted Selectivity in Protonation Enables the Mild Deuteration of Arenes through Catalytic Amounts of Bronsted Acids in Deuterated Methanol
Fischer, Oliver,Hubert, Anja,Heinrich, Markus R.
, p. 11856 - 11866 (2020/10/23)
Taking advantage of the "differentiating effect"of the solvent methanol, deuterations of electron-rich aromatic systems can be carried out under mild acid catalysis and thus under far milder conditions than known so far. The exceptional functional group t
Synthesis of C-2 and C-4 deuterium-labeled estradiol-17β
Ferraboschi,Ravasi,Santaniello
, p. 777 - 782 (2007/10/02)
Estradiol-17β labeled with deuterium in the positions 2 or 4 can be prepared from 2-chloromercurio-1,3,5(10)-estratriene-3,17β -diol 3-methyl ether 17-acetate or 4-chloromercurio-1,3,5(10)-estratriene-3,17β -diol, respectively, in refluxing CH3COO2H/2H2O. The same reaction performed on 4-acetoxymercurio1,3,5(10)-estratriene-3,17β -diol afforded 2,4-dideuterio-estradiol-17β in good yields.
