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Late-Stage Molecular Editing Enabled by Ketone Chain-Walking Isomerization

[Image: see text] Herein, a method for the isomerization of ketones in a manner akin to the chain-walking reaction of alkenes is described. Widely available and inexpensive pyrrolidine and elemental sulfur are deployed as catalysts to achieve this reversible transformation. Key to the utility of thi...

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Autores principales: Brägger, Yannick, Green, Ori, Bhawal, Benjamin N., Morandi, Bill
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510328/
https://www.ncbi.nlm.nih.gov/pubmed/37640367
http://dx.doi.org/10.1021/jacs.3c05680
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author Brägger, Yannick
Green, Ori
Bhawal, Benjamin N.
Morandi, Bill
author_facet Brägger, Yannick
Green, Ori
Bhawal, Benjamin N.
Morandi, Bill
author_sort Brägger, Yannick
collection PubMed
description [Image: see text] Herein, a method for the isomerization of ketones in a manner akin to the chain-walking reaction of alkenes is described. Widely available and inexpensive pyrrolidine and elemental sulfur are deployed as catalysts to achieve this reversible transformation. Key to the utility of this approach was the elucidation of a stereochemical model to determine the thermodynamically favored product of the reaction and the kinetic selectivity observed. With the distinct selectivity profile of our ketone chain-walking process, the isomerization of various steroids was demonstrated to rapidly access novel steroids with “unnatural” oxidation patterns.
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spelling pubmed-105103282023-09-21 Late-Stage Molecular Editing Enabled by Ketone Chain-Walking Isomerization Brägger, Yannick Green, Ori Bhawal, Benjamin N. Morandi, Bill J Am Chem Soc [Image: see text] Herein, a method for the isomerization of ketones in a manner akin to the chain-walking reaction of alkenes is described. Widely available and inexpensive pyrrolidine and elemental sulfur are deployed as catalysts to achieve this reversible transformation. Key to the utility of this approach was the elucidation of a stereochemical model to determine the thermodynamically favored product of the reaction and the kinetic selectivity observed. With the distinct selectivity profile of our ketone chain-walking process, the isomerization of various steroids was demonstrated to rapidly access novel steroids with “unnatural” oxidation patterns. American Chemical Society 2023-08-28 /pmc/articles/PMC10510328/ /pubmed/37640367 http://dx.doi.org/10.1021/jacs.3c05680 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Brägger, Yannick
Green, Ori
Bhawal, Benjamin N.
Morandi, Bill
Late-Stage Molecular Editing Enabled by Ketone Chain-Walking Isomerization
title Late-Stage Molecular Editing Enabled by Ketone Chain-Walking Isomerization
title_full Late-Stage Molecular Editing Enabled by Ketone Chain-Walking Isomerization
title_fullStr Late-Stage Molecular Editing Enabled by Ketone Chain-Walking Isomerization
title_full_unstemmed Late-Stage Molecular Editing Enabled by Ketone Chain-Walking Isomerization
title_short Late-Stage Molecular Editing Enabled by Ketone Chain-Walking Isomerization
title_sort late-stage molecular editing enabled by ketone chain-walking isomerization
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510328/
https://www.ncbi.nlm.nih.gov/pubmed/37640367
http://dx.doi.org/10.1021/jacs.3c05680
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