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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...

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Autores principales: Hokamp, Tobias, Wirth, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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