Ir(iii)-catalyzed ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents

Transition-metal-catalyzed C-H alkylation reactions directed by aldehydes or ketones have been largely restricted to electronically activated alkenes. Herein, we report a general protocol for the Ir(iii)-catalyzed C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents as the coupli...

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Veröffentlicht in:Chemical science (Cambridge) 2018-12, Vol.9 (48), p.8951-8956
Hauptverfasser: Chen, Xiao-Yang, Sorensen, Erik J
Format: Artikel
Sprache:eng
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Zusammenfassung:Transition-metal-catalyzed C-H alkylation reactions directed by aldehydes or ketones have been largely restricted to electronically activated alkenes. Herein, we report a general protocol for the Ir(iii)-catalyzed C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents as the coupling partner. Featuring aniline as an inexpensive catalytic ligand, the method was compatible with a wide variety of benzaldehydes, heterocyclic aldehydes, potassium alkyltrifluoroborates as well as a few α,β-unsaturated aldehydes. An X-ray crystal structure of a benzaldehyde C-H iridation intermediate was also successfully obtained.
ISSN:2041-6520
2041-6539
DOI:10.1039/c8sc03606c