118872-62-1Relevant articles and documents
Convenient and efficient deuteration of functionalized aromatics with deuterium oxide: Catalysis by cycloocta-1,5-dienyliridium(I) 1,3-dionates
McAuley,Hickey,Kingston,Jones,Lockley,Mather,Spink,Thompson,Wilkinson
, p. 1191 - 1204 (2003)
Aromatic compounds bearing an ortho-directing substituent may be deuterated by exchange with deuterium oxide in the presence of a range of cycloocta-1,5-dienyliridium(I)1,3-dionate catalysts. The exchange takes place in several dipolar aprotic solvents an
Labelling of anilines, benzylamines and some N-heterocyclics using cycloocta-1,5-dienyliridium(I) -1,1,1,5,5,5-hexafluoro-pentan-2,4-dionate and isotopic hydrogen gas in DMF or DMA
Garman,Hickey,Kingston,McAuley,Jones,Lockley,Mather,Wilkinson
, p. 75 - 84 (2005)
A wide range of anilines, benzylamines and some N-heterocyclics can be ortho-deuterated at room temperature using deuterium gas and cycloocta-1,5-dienyliridium(I)-1,1,1,5,5,5-hexafluoropentan-2,4-dionate in DMF or DMA. The method is applicable to labellin
Ruthenium(II)-Catalyzed Hydrogen Isotope Exchange of Pharmaceutical Drugs by C?H Deuteration and C?H Tritiation
Müller, Valentin,Weck, Remo,Derdau, Volker,Ackermann, Lutz
, p. 100 - 104 (2019/12/24)
Well-defined ruthenium(II) biscarboxylate complexes enabled selective ortho-deuteration with weakly-coordinating, synthetically useful carboxylic acid with outstanding levels of isotopic labeling. The robust nature of the catalytic system was reflected by