Three‐Component Synthesis of γ‐Amino Esters with α‐Quaternary Carbon Centers via NHC/Photoredox Dual Catalysis
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Wiley Open Access
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| Format: | Artículo Open Access |
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Wiley
2025
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| _version_ | 1867018046906826752 |
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| author | Adam X. Wayment Karl A. Scheidt |
| author_facet | Adam X. Wayment Karl A. Scheidt Adam X. Wayment Karl A. Scheidt |
| collection | Wiley Open Access |
| contents | Three‐Component Synthesis of γ‐Amino Esters with α‐Quaternary Carbon Centers via NHC/Photoredox Dual Catalysis Adam X. Wayment Karl A. Scheidt Advanced Synthesis & Catalysis γ‐Amino acid derivatives are important motifs in medicinal chemistry and have shown wide applicability as inhibitory neurotransmitters. An important class of these compounds feature α,α‐disubstitution. However, established routes for the direct synthesis of γ‐amino esters bearing α‐quaternary centers are severely limited in both number of available routes and scope of the transformation. Herein a method is presented for the three‐component synthesis of α,α‐disubstituted γ‐amino esters via N‐heterocyclic carbene/photoredox dual catalysis. This reaction involves in situ formation of an acyl azolium ester which undergoes photocatalytic reduction to the key stabilized alkoxycarbonyl radical. This methodology is shown to be capable of synthesizing a wide variety of γ‐amino esters with various α‐quaternary centers in moderate to good yields, including a derivative of the drug loperamide. The diversity of products that can be synthesized facilitates the rapid generation of libraries of γ‐amino acid derived compounds. 10.1002/adsc.70013 http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| doi_str_mv | 10.1002/adsc.70013 |
| format | Artículo Open Access |
| id | wiley_oa_10_1002_adsc_70013 |
| institution | Wiley Open Access |
| license_str_mv | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| publishDate | 2025 |
| publisher | Wiley |
| record_format | wiley_oa |
| spellingShingle | Three‐Component Synthesis of γ‐Amino Esters with α‐Quaternary Carbon Centers via NHC/Photoredox Dual Catalysis Adam X. Wayment Karl A. Scheidt Advanced Synthesis & Catalysis Three‐Component Synthesis of γ‐Amino Esters with α‐Quaternary Carbon Centers via NHC/Photoredox Dual Catalysis Adam X. Wayment Karl A. Scheidt Advanced Synthesis & Catalysis γ‐Amino acid derivatives are important motifs in medicinal chemistry and have shown wide applicability as inhibitory neurotransmitters. An important class of these compounds feature α,α‐disubstitution. However, established routes for the direct synthesis of γ‐amino esters bearing α‐quaternary centers are severely limited in both number of available routes and scope of the transformation. Herein a method is presented for the three‐component synthesis of α,α‐disubstituted γ‐amino esters via N‐heterocyclic carbene/photoredox dual catalysis. This reaction involves in situ formation of an acyl azolium ester which undergoes photocatalytic reduction to the key stabilized alkoxycarbonyl radical. This methodology is shown to be capable of synthesizing a wide variety of γ‐amino esters with various α‐quaternary centers in moderate to good yields, including a derivative of the drug loperamide. The diversity of products that can be synthesized facilitates the rapid generation of libraries of γ‐amino acid derived compounds. 10.1002/adsc.70013 http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| title | Three‐Component Synthesis of γ‐Amino Esters with α‐Quaternary Carbon Centers via NHC/Photoredox Dual Catalysis |
| topic | Advanced Synthesis & Catalysis |
| url | https://advanced.onlinelibrary.wiley.com/doi/10.1002/adsc.70013 |