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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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dc.contributor.authorChen, Xiao-Yang-
dc.contributor.authorSorensen, Erik J.-
dc.date.accessioned2020-10-30T19:05:21Z-
dc.date.available2020-10-30T19:05:21Z-
dc.date.issued2018-03-01en_US
dc.identifier.citationChen, 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/c8sc03606cen_US
dc.identifier.issn2041-6520-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/pr1zj7b-
dc.descriptionVolume 9, Issue 48, 2018, Pages 8951-8956.First published on 3rd October 2018.en_US
dc.description.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.en_US
dc.format.extent9.48: 8951 - 8956en_US
dc.language.isoenen_US
dc.relation.ispartofChemical Scienceen_US
dc.rightsFinal published version. This is an open access article.en_US
dc.titleIr(iii)-catalyzed: Ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagentsen_US
dc.typeJournal Articleen_US
dc.identifier.doidoi:10.1039/c8sc03606c-
dc.identifier.eissn2041-6539-
pu.type.symplectichttp://www.symplectic.co.uk/publications/atom-terms/1.0/journal-articleen_US

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