Access to Hetero-Benzyl Scaffolds via Transient-Ligand-Enabled Direct γ-C(sp 3 )-H Arylation of 3-Methylheteroarene-2-Carbaldehydes
An efficient and straightforward method has been developed for the synthesis of β-benzyl-substituted 5-membered heterocyclic carbaldehydes via transient directing-group-enabled direct γ-C(sp )-H arylation of 3-methylheteroarene-2-carbaldehydes. A wide range of 3-methylheteroarene carbaldehydes under...
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Veröffentlicht in: | Journal of organic chemistry 2020-06, Vol.85 (11), p.6924-6934 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | An efficient and straightforward method has been developed for the synthesis of β-benzyl-substituted 5-membered heterocyclic carbaldehydes via transient directing-group-enabled direct γ-C(sp
)-H arylation of 3-methylheteroarene-2-carbaldehydes. A wide range of 3-methylheteroarene carbaldehydes undergo coupling with a variety of aryl iodides, including less reactive iodo pyridine derivatives to provide a library of highly selective functionalized products in good to excellent yields. Some of these products have been successfully utilized in synthesizing useful synthetic intermediates. |
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ISSN: | 0022-3263 1520-6904 |
DOI: | 10.1021/acs.joc.0c00154 |