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Hypervalent Iodine(III)‐Catalysed Enantioselective α‐Acetoxylation of Ketones
An enantioselective catalytic synthesis of α‐acetoxylated ketones through I(I)/I(III) catalysis using a resorcinol/lactamide‐based chiral iodoarene is reported. Catalyst turnover by in situ generation of the active iodine(III) derivative is achieved by oxidation with mCPBA in the presence of acetic...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496773/ https://www.ncbi.nlm.nih.gov/pubmed/32233006 http://dx.doi.org/10.1002/chem.202000927 |
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author | Hokamp, Tobias Wirth, Thomas |
author_facet | Hokamp, Tobias Wirth, Thomas |
author_sort | Hokamp, Tobias |
collection | PubMed |
description | An enantioselective catalytic synthesis of α‐acetoxylated ketones through I(I)/I(III) catalysis using a resorcinol/lactamide‐based chiral iodoarene is reported. Catalyst turnover by in situ generation of the active iodine(III) derivative is achieved by oxidation with mCPBA in the presence of acetic acid. The prior transformation of ketones to easily accessible acetyl enol ethers is beneficial and yields up to 97 % with enantioselectivities up to 88 % ee are obtained using only low catalyst loadings of only 5 mol % under mild reaction conditions. |
format | Online Article Text |
id | pubmed-7496773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74967732020-09-25 Hypervalent Iodine(III)‐Catalysed Enantioselective α‐Acetoxylation of Ketones Hokamp, Tobias Wirth, Thomas Chemistry Communications An enantioselective catalytic synthesis of α‐acetoxylated ketones through I(I)/I(III) catalysis using a resorcinol/lactamide‐based chiral iodoarene is reported. Catalyst turnover by in situ generation of the active iodine(III) derivative is achieved by oxidation with mCPBA in the presence of acetic acid. The prior transformation of ketones to easily accessible acetyl enol ethers is beneficial and yields up to 97 % with enantioselectivities up to 88 % ee are obtained using only low catalyst loadings of only 5 mol % under mild reaction conditions. John Wiley and Sons Inc. 2020-07-20 2020-08-17 /pmc/articles/PMC7496773/ /pubmed/32233006 http://dx.doi.org/10.1002/chem.202000927 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Hokamp, Tobias Wirth, Thomas Hypervalent Iodine(III)‐Catalysed Enantioselective α‐Acetoxylation of Ketones |
title | Hypervalent Iodine(III)‐Catalysed Enantioselective α‐Acetoxylation of Ketones |
title_full | Hypervalent Iodine(III)‐Catalysed Enantioselective α‐Acetoxylation of Ketones |
title_fullStr | Hypervalent Iodine(III)‐Catalysed Enantioselective α‐Acetoxylation of Ketones |
title_full_unstemmed | Hypervalent Iodine(III)‐Catalysed Enantioselective α‐Acetoxylation of Ketones |
title_short | Hypervalent Iodine(III)‐Catalysed Enantioselective α‐Acetoxylation of Ketones |
title_sort | hypervalent iodine(iii)‐catalysed enantioselective α‐acetoxylation of ketones |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496773/ https://www.ncbi.nlm.nih.gov/pubmed/32233006 http://dx.doi.org/10.1002/chem.202000927 |
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