The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Benzylic C−H acylation by cooperative NHC and photoredox catalysis
Open accessAbstract
Methods that enable site selective acylation of sp 3 C-H bonds in complex organic molecules are not well explored, particularly if compared with analogous transformations of aromatic and vinylic sp 2 C-H bonds. We report herein a direct acylation of benzylic C-H bonds by merging N-heterocyclic carbene (NHC) and photoredox catalysis. The method allows the preparation of a diverse range of benzylic ketones with good functional group tolerance under mild conditions. The reaction can be used to install acyl groups on highly functionalized natural product derived compounds and the C-H functionalization works with excellent site selectivity. The combination of NHC and photoredox catalysis offers options in preparing benzyl aryl ketones.
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Prier, C. K., Rankic, D. A., & MacMillan, D. W. C. (2013) · Chemical Reviews · doi:10.1021/cr300503r · Cited by 9,590
Cited by
Photocatalytic Late-Stage C–H Functionalization
Bellotti, P., Huang, H.-M., Faber, T., & Glorius, F. (2023) · Chemical Reviews · doi:10.1021/acs.chemrev.2c00478 · Cited by 623
Liu, K., Schwenzer, M., & Studer, A. (2022) · ACS Catalysis · doi:10.1021/acscatal.2c03996 · Cited by 325
Self-citation
Metadata
- Authors
- Meng, Q.-Y., Lezius, L., & Studer, A.
- Venue
- Nature Communications
- Published
- 2021-04-06
- Volume
- 12
- Issue
- 1
- Pages
- 2068-2068
- ISSN
- 2041-1723 (ISSN-L)
- OpenAlex
- W3152410730
- Cited by
- 189
- References
- 1
- FWCI
- 13.32
- Type
- journal article
- Language
- en
- Open access
- gold
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