Site-selective deuteration of N-heterocycles via iridium-catalyzed hydrogen isotope exchange
Kerr, William J. and Lindsay, David M. and Owens, Philippa K. and Reid, Marc and Tuttle, Tell and Campos, Sébastien (2017) Site-selective deuteration of N-heterocycles via iridium-catalyzed hydrogen isotope exchange. ACS Catalysis, 7 (10). 7182–7186. ISSN 2155-5435 (https://doi.org/10.1021/acscatal.7b02682)
Preview |
Text.
Filename: Kerr_etal_ACSC_2017_Site_selective_deuteration_of_N_heterocycles_via_iridium.pdf
Final Published Version License: Download (1MB)| Preview |
Abstract
The application of iridium(I) NHC/phosphine catalysts has delivered highly selective deuteration of indole, azaindole, and pyrrole N-heterocycles, which represent an important and relatively underexplored class of labeling substrates. Common N-protecting groups have been used to selectively direct C–H activation, and can be removed under mild conditions with retention of the deuterium label. The method is exemplified by the labeling of drug molecule Sumatriptan. Complementary DFT studies have been conducted to facilitate the rationalization of the very good selectivity offered by the mild and convenient labeling process.
ORCID iDs
Kerr, William J. ORCID: https://orcid.org/0000-0002-1332-785X, Lindsay, David M. ORCID: https://orcid.org/0000-0003-4498-5094, Owens, Philippa K. ORCID: https://orcid.org/0000-0002-9369-2899, Reid, Marc ORCID: https://orcid.org/0000-0003-4394-3132, Tuttle, Tell and Campos, Sébastien;-
-
Item type: Article ID code: 61885 Dates: DateEvent6 October 2017Published11 September 2017Published Online8 September 2017AcceptedSubjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry
Technology and Innovation Centre > BionanotechnologyDepositing user: Pure Administrator Date deposited: 02 Oct 2017 09:35 Last modified: 16 Nov 2024 13:58 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/61885