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- Publisher Website: 10.1021/jacs.7b02196
- Scopus: eid_2-s2.0-85018290222
- PMID: 28391681
- WOS: WOS:000400321500023
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Article: Ligand-Enabled Pd(II)-Catalyzed Bromination and Iodination of C(sp3)-H Bonds
| Title | Ligand-Enabled Pd(II)-Catalyzed Bromination and Iodination of C(sp3)-H Bonds |
|---|---|
| Authors | |
| Issue Date | 2017 |
| Citation | Journal of the American Chemical Society, 2017, v. 139, n. 16, p. 5724-5727 How to Cite? |
| Abstract | © 2017 American Chemical Society. We herein report the palladium(II)-catalyzed bromination and iodination of a variety of α-hydrogen-containing carboxylic acid and amino acid-derived amides. These reactions are exclusively enabled by quinoline-type ligands. The halogenated products obtained in this reaction are highly versatile and rapidly undergo further diversification. Further, we report the first example of a free carboxylic acid-directed Pd(II)-catalyzed C(sp3)-H bromination, enabled by quinoline ligands. |
| Persistent Identifier | http://hdl.handle.net/10722/276513 |
| ISSN | 2023 Impact Factor: 14.4 2023 SCImago Journal Rankings: 5.489 |
| ISI Accession Number ID |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Zhu, Ru Yi | - |
| dc.contributor.author | Saint-Denis, Tyler G. | - |
| dc.contributor.author | Shao, Ying | - |
| dc.contributor.author | He, Jian | - |
| dc.contributor.author | Sieber, Joshua D. | - |
| dc.contributor.author | Senanayake, Chris H. | - |
| dc.contributor.author | Yu, Jin Quan | - |
| dc.date.accessioned | 2019-09-18T08:33:50Z | - |
| dc.date.available | 2019-09-18T08:33:50Z | - |
| dc.date.issued | 2017 | - |
| dc.identifier.citation | Journal of the American Chemical Society, 2017, v. 139, n. 16, p. 5724-5727 | - |
| dc.identifier.issn | 0002-7863 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/276513 | - |
| dc.description.abstract | © 2017 American Chemical Society. We herein report the palladium(II)-catalyzed bromination and iodination of a variety of α-hydrogen-containing carboxylic acid and amino acid-derived amides. These reactions are exclusively enabled by quinoline-type ligands. The halogenated products obtained in this reaction are highly versatile and rapidly undergo further diversification. Further, we report the first example of a free carboxylic acid-directed Pd(II)-catalyzed C(sp3)-H bromination, enabled by quinoline ligands. | - |
| dc.language | eng | - |
| dc.relation.ispartof | Journal of the American Chemical Society | - |
| dc.title | Ligand-Enabled Pd(II)-Catalyzed Bromination and Iodination of C(sp3)-H Bonds | - |
| dc.type | Article | - |
| dc.description.nature | link_to_subscribed_fulltext | - |
| dc.identifier.doi | 10.1021/jacs.7b02196 | - |
| dc.identifier.pmid | 28391681 | - |
| dc.identifier.scopus | eid_2-s2.0-85018290222 | - |
| dc.identifier.volume | 139 | - |
| dc.identifier.issue | 16 | - |
| dc.identifier.spage | 5724 | - |
| dc.identifier.epage | 5727 | - |
| dc.identifier.eissn | 1520-5126 | - |
| dc.identifier.isi | WOS:000400321500023 | - |
| dc.identifier.issnl | 0002-7863 | - |