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Transition metal-catalysed carbene- and nitrene transfer to carbon monoxide and isocyanides
Transition metal-catalysed carbene- and nitrene transfer to the C1-building blocks carbon monoxide and isocyanides provides heteroallenes (i.e. ketenes, isocyanates, ketenimines and carbodiimides). These are versatile and reactive compounds allowing in situ transformation towards numerous functional...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580617/ https://www.ncbi.nlm.nih.gov/pubmed/35748338 http://dx.doi.org/10.1039/d1cs00305d |
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author | Roose, T. R. Verdoorn, D. S. Mampuys, P. Ruijter, E. Maes, B. U. W. Orru, R. V. A. |
author_facet | Roose, T. R. Verdoorn, D. S. Mampuys, P. Ruijter, E. Maes, B. U. W. Orru, R. V. A. |
author_sort | Roose, T. R. |
collection | PubMed |
description | Transition metal-catalysed carbene- and nitrene transfer to the C1-building blocks carbon monoxide and isocyanides provides heteroallenes (i.e. ketenes, isocyanates, ketenimines and carbodiimides). These are versatile and reactive compounds allowing in situ transformation towards numerous functional groups and organic compounds, including heterocycles. Both one-pot and tandem processes have been developed providing valuable synthetic methods for the organic chemistry toolbox. This review discusses all known transition metal-catalysed carbene- and nitrene transfer reactions towards carbon monoxide and isocyanides and in situ transformation of the heteroallenes hereby obtained, with a special focus on the general mechanistic considerations. |
format | Online Article Text |
id | pubmed-9580617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-95806172022-10-31 Transition metal-catalysed carbene- and nitrene transfer to carbon monoxide and isocyanides Roose, T. R. Verdoorn, D. S. Mampuys, P. Ruijter, E. Maes, B. U. W. Orru, R. V. A. Chem Soc Rev Chemistry Transition metal-catalysed carbene- and nitrene transfer to the C1-building blocks carbon monoxide and isocyanides provides heteroallenes (i.e. ketenes, isocyanates, ketenimines and carbodiimides). These are versatile and reactive compounds allowing in situ transformation towards numerous functional groups and organic compounds, including heterocycles. Both one-pot and tandem processes have been developed providing valuable synthetic methods for the organic chemistry toolbox. This review discusses all known transition metal-catalysed carbene- and nitrene transfer reactions towards carbon monoxide and isocyanides and in situ transformation of the heteroallenes hereby obtained, with a special focus on the general mechanistic considerations. The Royal Society of Chemistry 2022-06-24 /pmc/articles/PMC9580617/ /pubmed/35748338 http://dx.doi.org/10.1039/d1cs00305d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Roose, T. R. Verdoorn, D. S. Mampuys, P. Ruijter, E. Maes, B. U. W. Orru, R. V. A. Transition metal-catalysed carbene- and nitrene transfer to carbon monoxide and isocyanides |
title | Transition metal-catalysed carbene- and nitrene transfer to carbon monoxide and isocyanides |
title_full | Transition metal-catalysed carbene- and nitrene transfer to carbon monoxide and isocyanides |
title_fullStr | Transition metal-catalysed carbene- and nitrene transfer to carbon monoxide and isocyanides |
title_full_unstemmed | Transition metal-catalysed carbene- and nitrene transfer to carbon monoxide and isocyanides |
title_short | Transition metal-catalysed carbene- and nitrene transfer to carbon monoxide and isocyanides |
title_sort | transition metal-catalysed carbene- and nitrene transfer to carbon monoxide and isocyanides |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580617/ https://www.ncbi.nlm.nih.gov/pubmed/35748338 http://dx.doi.org/10.1039/d1cs00305d |
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