Literature DB >> 25252806

Regioselective ruthenium catalysed H-D exchange using D2O as the deuterium source.

Lorenzo Piola1, José A Fernández-Salas, Simone Manzini, Steven P Nolan.   

Abstract

An efficient and convenient ruthenium catalysed method for a regiospecific H/D exchange using D2O is described. Organic moieties such as pyridine, oxazole, imidazole, pyrazole, ester, ketone and carboxylic acid have been found effective directing groups in this transformation. In addition, the deuteration of the enantiopure (S)-Ketoprofen leads to the incorporation of three deuterium atoms with retention of molecular chirality.

Entities:  

Year:  2014        PMID: 25252806     DOI: 10.1039/c4ob01798f

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

Review 1.  Indenylmetal Catalysis in Organic Synthesis.

Authors:  Barry M Trost; Michael C Ryan
Journal:  Angew Chem Int Ed Engl       Date:  2017-01-27       Impact factor: 15.336

2.  H-D exchange in deuterated trifluoroacetic acid via ligand-directed NHC-palladium catalysis: a powerful method for deuteration of aromatic ketones, amides, and amino acids.

Authors:  Richard Giles; Green Ahn; Kyung Woon Jung
Journal:  Tetrahedron Lett       Date:  2015-11-04       Impact factor: 2.415

3.  Mild, Selective Ru-Catalyzed Deuteration Using D2 O as a Deuterium Source.

Authors:  Pascal Eisele; Franziska Ullwer; Sven Scholz; Bernd Plietker
Journal:  Chemistry       Date:  2019-11-03       Impact factor: 5.236

  3 in total

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