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Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products**
The rhodium-catalyzed methylation of ketones has been accomplished using methanol as the methylating agent and the hydrogen-borrowing method. The sequence is notable for the relatively low temperatures that are required and for the ability of the reaction system to form α-branched products with ease...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4138999/ https://www.ncbi.nlm.nih.gov/pubmed/24288297 http://dx.doi.org/10.1002/anie.201307950 |
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author | Chan, Louis K M Poole, Darren L Shen, Di Healy, Mark P Donohoe, Timothy J |
author_facet | Chan, Louis K M Poole, Darren L Shen, Di Healy, Mark P Donohoe, Timothy J |
author_sort | Chan, Louis K M |
collection | PubMed |
description | The rhodium-catalyzed methylation of ketones has been accomplished using methanol as the methylating agent and the hydrogen-borrowing method. The sequence is notable for the relatively low temperatures that are required and for the ability of the reaction system to form α-branched products with ease. Doubly alkylated ketones can be prepared from methyl ketones and two different alcohols by using a sequential one-pot iridium- and rhodium-catalyzed process. |
format | Online Article Text |
id | pubmed-4138999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-41389992014-09-22 Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products** Chan, Louis K M Poole, Darren L Shen, Di Healy, Mark P Donohoe, Timothy J Angew Chem Int Ed Engl Communications The rhodium-catalyzed methylation of ketones has been accomplished using methanol as the methylating agent and the hydrogen-borrowing method. The sequence is notable for the relatively low temperatures that are required and for the ability of the reaction system to form α-branched products with ease. Doubly alkylated ketones can be prepared from methyl ketones and two different alcohols by using a sequential one-pot iridium- and rhodium-catalyzed process. WILEY-VCH Verlag 2014-01-13 2013-11-29 /pmc/articles/PMC4138999/ /pubmed/24288297 http://dx.doi.org/10.1002/anie.201307950 Text en © 2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Chan, Louis K M Poole, Darren L Shen, Di Healy, Mark P Donohoe, Timothy J Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products** |
title | Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products** |
title_full | Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products** |
title_fullStr | Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products** |
title_full_unstemmed | Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products** |
title_short | Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products** |
title_sort | rhodium-catalyzed ketone methylation using methanol under mild conditions: formation of α-branched products** |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4138999/ https://www.ncbi.nlm.nih.gov/pubmed/24288297 http://dx.doi.org/10.1002/anie.201307950 |
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