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- Publisher Website: 10.1021/jacs.5b04088
- Scopus: eid_2-s2.0-84935069572
- PMID: 26001406
- WOS: WOS:000356322300024
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Article: Ligand-Enabled Stereoselective β-C(sp3)-H Fluorination: Synthesis of Unnatural Enantiopure anti-β-Fluoro-α-amino Acids
| Title | Ligand-Enabled Stereoselective β-C(sp3)-H Fluorination: Synthesis of Unnatural Enantiopure anti-β-Fluoro-α-amino Acids |
|---|---|
| Authors | |
| Issue Date | 2015 |
| Citation | Journal of the American Chemical Society, 2015, v. 137, n. 22, p. 7067-7070 How to Cite? |
| Abstract | © 2015 American Chemical Society. A quinoline-based ligand was shown to promote palladium-catalyzed β-C(sp3)-H fluorination for the first time. A range of unnatural enantiopure fluorinated α-amino acids were obtained through sequential β-C(sp3)-H arylation and subsequent stereoselective fluorination from readily available l-alanine. |
| Persistent Identifier | http://hdl.handle.net/10722/276691 |
| 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 | Tanaka, Keita | - |
| dc.contributor.author | Li, Gen Cheng | - |
| dc.contributor.author | He, Jian | - |
| dc.contributor.author | Fu, Hai Yan | - |
| dc.contributor.author | Li, Su Hua | - |
| dc.contributor.author | Yu, Jin Quan | - |
| dc.date.accessioned | 2019-09-18T08:34:22Z | - |
| dc.date.available | 2019-09-18T08:34:22Z | - |
| dc.date.issued | 2015 | - |
| dc.identifier.citation | Journal of the American Chemical Society, 2015, v. 137, n. 22, p. 7067-7070 | - |
| dc.identifier.issn | 0002-7863 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/276691 | - |
| dc.description.abstract | © 2015 American Chemical Society. A quinoline-based ligand was shown to promote palladium-catalyzed β-C(sp3)-H fluorination for the first time. A range of unnatural enantiopure fluorinated α-amino acids were obtained through sequential β-C(sp3)-H arylation and subsequent stereoselective fluorination from readily available l-alanine. | - |
| dc.language | eng | - |
| dc.relation.ispartof | Journal of the American Chemical Society | - |
| dc.title | Ligand-Enabled Stereoselective β-C(sp3)-H Fluorination: Synthesis of Unnatural Enantiopure anti-β-Fluoro-α-amino Acids | - |
| dc.type | Article | - |
| dc.description.nature | link_to_subscribed_fulltext | - |
| dc.identifier.doi | 10.1021/jacs.5b04088 | - |
| dc.identifier.pmid | 26001406 | - |
| dc.identifier.scopus | eid_2-s2.0-84935069572 | - |
| dc.identifier.volume | 137 | - |
| dc.identifier.issue | 22 | - |
| dc.identifier.spage | 7067 | - |
| dc.identifier.epage | 7070 | - |
| dc.identifier.eissn | 1520-5126 | - |
| dc.identifier.isi | WOS:000356322300024 | - |
| dc.identifier.issnl | 0002-7863 | - |