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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 ortho C–H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents as the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6301268/ https://www.ncbi.nlm.nih.gov/pubmed/30647887 http://dx.doi.org/10.1039/c8sc03606c |
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author | Chen, Xiao-Yang Sorensen, Erik J. |
author_facet | Chen, Xiao-Yang Sorensen, Erik J. |
author_sort | Chen, Xiao-Yang |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6301268 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-63012682019-01-15 Ir(iii)-catalyzed ortho C–H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents Chen, Xiao-Yang Sorensen, Erik J. Chem Sci 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. Royal Society of Chemistry 2018-10-03 /pmc/articles/PMC6301268/ /pubmed/30647887 http://dx.doi.org/10.1039/c8sc03606c Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Chen, Xiao-Yang Sorensen, Erik J. 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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title_full | Ir(iii)-catalyzed ortho C–H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents
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title_fullStr | Ir(iii)-catalyzed ortho C–H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents
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title_full_unstemmed | Ir(iii)-catalyzed ortho C–H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents
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title_short | Ir(iii)-catalyzed ortho C–H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents
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title_sort | ir(iii)-catalyzed ortho c–h alkylations of (hetero)aromatic aldehydes using alkyl boron reagents |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6301268/ https://www.ncbi.nlm.nih.gov/pubmed/30647887 http://dx.doi.org/10.1039/c8sc03606c |
work_keys_str_mv | AT chenxiaoyang iriiicatalyzedorthochalkylationsofheteroaromaticaldehydesusingalkylboronreagents AT sorensenerikj iriiicatalyzedorthochalkylationsofheteroaromaticaldehydesusingalkylboronreagents |