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Carbon monoxide and hydrogen (syngas) as a C1-building block for selective catalytic methylation
A catalytic reaction using syngas (CO/H(2)) as feedstock for the selective β-methylation of alcohols was developed whereby carbon monoxide acts as a C1 source and hydrogen gas as a reducing agent. The overall transformation occurs through an intricate network of metal-catalyzed and base-mediated rea...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179066/ https://www.ncbi.nlm.nih.gov/pubmed/34163864 http://dx.doi.org/10.1039/d0sc05404f |
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author | Kaithal, Akash Hölscher, Markus Leitner, Walter |
author_facet | Kaithal, Akash Hölscher, Markus Leitner, Walter |
author_sort | Kaithal, Akash |
collection | PubMed |
description | A catalytic reaction using syngas (CO/H(2)) as feedstock for the selective β-methylation of alcohols was developed whereby carbon monoxide acts as a C1 source and hydrogen gas as a reducing agent. The overall transformation occurs through an intricate network of metal-catalyzed and base-mediated reactions. The molecular complex [Mn(CO)(2)Br[HN(C(2)H(4)P(i)Pr(2))(2)]] 1 comprising earth-abundant manganese acts as the metal component in the catalytic system enabling the generation of formaldehyde from syngas in a synthetically useful reaction. This new syngas conversion opens pathways to install methyl branches at sp(3) carbon centers utilizing renewable feedstocks and energy for the synthesis of biologically active compounds, fine chemicals, and advanced biofuels. |
format | Online Article Text |
id | pubmed-8179066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81790662021-06-22 Carbon monoxide and hydrogen (syngas) as a C1-building block for selective catalytic methylation Kaithal, Akash Hölscher, Markus Leitner, Walter Chem Sci Chemistry A catalytic reaction using syngas (CO/H(2)) as feedstock for the selective β-methylation of alcohols was developed whereby carbon monoxide acts as a C1 source and hydrogen gas as a reducing agent. The overall transformation occurs through an intricate network of metal-catalyzed and base-mediated reactions. The molecular complex [Mn(CO)(2)Br[HN(C(2)H(4)P(i)Pr(2))(2)]] 1 comprising earth-abundant manganese acts as the metal component in the catalytic system enabling the generation of formaldehyde from syngas in a synthetically useful reaction. This new syngas conversion opens pathways to install methyl branches at sp(3) carbon centers utilizing renewable feedstocks and energy for the synthesis of biologically active compounds, fine chemicals, and advanced biofuels. The Royal Society of Chemistry 2020-11-20 /pmc/articles/PMC8179066/ /pubmed/34163864 http://dx.doi.org/10.1039/d0sc05404f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Kaithal, Akash Hölscher, Markus Leitner, Walter Carbon monoxide and hydrogen (syngas) as a C1-building block for selective catalytic methylation |
title | Carbon monoxide and hydrogen (syngas) as a C1-building block for selective catalytic methylation |
title_full | Carbon monoxide and hydrogen (syngas) as a C1-building block for selective catalytic methylation |
title_fullStr | Carbon monoxide and hydrogen (syngas) as a C1-building block for selective catalytic methylation |
title_full_unstemmed | Carbon monoxide and hydrogen (syngas) as a C1-building block for selective catalytic methylation |
title_short | Carbon monoxide and hydrogen (syngas) as a C1-building block for selective catalytic methylation |
title_sort | carbon monoxide and hydrogen (syngas) as a c1-building block for selective catalytic methylation |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179066/ https://www.ncbi.nlm.nih.gov/pubmed/34163864 http://dx.doi.org/10.1039/d0sc05404f |
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