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

Author(s): Chen, Xiao-Yang; Sorensen, Erik J.

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Abstract: © 2018 The Royal Society of Chemistry. 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 ortho 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 ortho C-H iridation intermediate was also successfully obtained.
Publication Date: 1-Mar-2018
Citation: Chen, X.Y., Sorensen, E.J. (2018). Ir(iii)-catalyzed: Ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents. Chemical Science, 9 (48), 8951 - 8956. doi:10.1039/c8sc03606c
DOI: doi:10.1039/c8sc03606c
ISSN: 2041-6520
EISSN: 2041-6539
Pages: 9.48: 8951 - 8956
Type of Material: Journal Article
Journal/Proceeding Title: Chemical Science
Version: Final published version. This is an open access article.
Notes: Volume 9, Issue 48, 2018, Pages 8951-8956.First published on 3rd October 2018.



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