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
Hauptverfasser: Reddy, Chennakesava, Shaikh, Javed Y, Bhat, Ramakrishna G
Format: Artikel
Sprache:eng
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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.
ISSN:0022-3263
1520-6904
DOI:10.1021/acs.joc.0c00154