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- Scopus: eid_2-s2.0-85058491387
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Article: Ir(iii)-catalyzed: Ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents
Title | Ir(iii)-catalyzed: Ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents |
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Authors | |
Issue Date | 2018 |
Citation | Chemical Science, 2018, v. 9, n. 48, p. 8951-8956 How to Cite? |
Abstract | 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. |
Persistent Identifier | http://hdl.handle.net/10722/327708 |
ISSN | 2023 Impact Factor: 7.6 2023 SCImago Journal Rankings: 2.333 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Chen, Xiao Yang | - |
dc.contributor.author | Sorensen, Erik J. | - |
dc.date.accessioned | 2023-04-24T05:09:24Z | - |
dc.date.available | 2023-04-24T05:09:24Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Chemical Science, 2018, v. 9, n. 48, p. 8951-8956 | - |
dc.identifier.issn | 2041-6520 | - |
dc.identifier.uri | http://hdl.handle.net/10722/327708 | - |
dc.description.abstract | 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. | - |
dc.language | eng | - |
dc.relation.ispartof | Chemical Science | - |
dc.title | Ir(iii)-catalyzed: Ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1039/c8sc03606c | - |
dc.identifier.scopus | eid_2-s2.0-85058491387 | - |
dc.identifier.volume | 9 | - |
dc.identifier.issue | 48 | - |
dc.identifier.spage | 8951 | - |
dc.identifier.epage | 8956 | - |
dc.identifier.eissn | 2041-6539 | - |
dc.identifier.isi | WOS:000453011400007 | - |