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Preparation of Deuterium Labeled Compounds by Pd/C-Al-D(2)O Facilitated Selective H-D Exchange Reactions

The chemo/regioselective H-D exchange of amino acids and synthetic building blocks by an environmentally benign Pd/C-Al-D(2)O catalytic system is described. Due to the importance of isotope labeled compounds in medicinal chemistry and structural biology, notably their use as improved drug candidates...

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Detalles Bibliográficos
Autores principales: Kokel, Anne, Kadish, Dora, Török, Béla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840159/
https://www.ncbi.nlm.nih.gov/pubmed/35163883
http://dx.doi.org/10.3390/molecules27030614
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author Kokel, Anne
Kadish, Dora
Török, Béla
author_facet Kokel, Anne
Kadish, Dora
Török, Béla
author_sort Kokel, Anne
collection PubMed
description The chemo/regioselective H-D exchange of amino acids and synthetic building blocks by an environmentally benign Pd/C-Al-D(2)O catalytic system is described. Due to the importance of isotope labeled compounds in medicinal chemistry and structural biology, notably their use as improved drug candidates and biological probes, the efficient and selective deuteration methods are of great interest. The approach is based on selective H-D exchange reactions where the deuterium source is simple D(2)O. D(2) gas is generated in situ from the reaction of aluminum and D(2)O, while the commercially available palladium catalyst assists the H-D exchange reaction. The high selectivity and efficiency, as well as the simplicity and safe nature of the procedure make this method an environmentally benign alternative to current alternatives.
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spelling pubmed-88401592022-02-13 Preparation of Deuterium Labeled Compounds by Pd/C-Al-D(2)O Facilitated Selective H-D Exchange Reactions Kokel, Anne Kadish, Dora Török, Béla Molecules Article The chemo/regioselective H-D exchange of amino acids and synthetic building blocks by an environmentally benign Pd/C-Al-D(2)O catalytic system is described. Due to the importance of isotope labeled compounds in medicinal chemistry and structural biology, notably their use as improved drug candidates and biological probes, the efficient and selective deuteration methods are of great interest. The approach is based on selective H-D exchange reactions where the deuterium source is simple D(2)O. D(2) gas is generated in situ from the reaction of aluminum and D(2)O, while the commercially available palladium catalyst assists the H-D exchange reaction. The high selectivity and efficiency, as well as the simplicity and safe nature of the procedure make this method an environmentally benign alternative to current alternatives. MDPI 2022-01-18 /pmc/articles/PMC8840159/ /pubmed/35163883 http://dx.doi.org/10.3390/molecules27030614 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kokel, Anne
Kadish, Dora
Török, Béla
Preparation of Deuterium Labeled Compounds by Pd/C-Al-D(2)O Facilitated Selective H-D Exchange Reactions
title Preparation of Deuterium Labeled Compounds by Pd/C-Al-D(2)O Facilitated Selective H-D Exchange Reactions
title_full Preparation of Deuterium Labeled Compounds by Pd/C-Al-D(2)O Facilitated Selective H-D Exchange Reactions
title_fullStr Preparation of Deuterium Labeled Compounds by Pd/C-Al-D(2)O Facilitated Selective H-D Exchange Reactions
title_full_unstemmed Preparation of Deuterium Labeled Compounds by Pd/C-Al-D(2)O Facilitated Selective H-D Exchange Reactions
title_short Preparation of Deuterium Labeled Compounds by Pd/C-Al-D(2)O Facilitated Selective H-D Exchange Reactions
title_sort preparation of deuterium labeled compounds by pd/c-al-d(2)o facilitated selective h-d exchange reactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840159/
https://www.ncbi.nlm.nih.gov/pubmed/35163883
http://dx.doi.org/10.3390/molecules27030614
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