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| dc.contributor.author | Prieto, Elena | |
| dc.contributor.author | Andrés, Celia | |
| dc.contributor.author | Nieto, Javier | |
| dc.date.accessioned | 2025-11-27T11:31:56Z | |
| dc.date.available | 2025-11-27T11:31:56Z | |
| dc.date.issued | 2025 | |
| dc.identifier.citation | Organic & Biomolecular Chemistry, 2025, vol. 23, p 10596-10605. | es |
| dc.identifier.issn | 1477-0520 | es |
| dc.identifier.uri | https://uvadoc.uva.es/handle/10324/80120 | |
| dc.description.abstract | The α-hydroxyamide moiety is an important structural component in a wide variety of biologically active compounds and natural products. Herein, we describe a highly efficient and practical approach towards chiral quaternary α-alkynyl-α-hydroxyamides by Me2Zn-mediated addition of terminal alkynes to α-keto amides. The desired products are obtained in good yields and enantioselectivities with broad substrate and reagent scopes. | es |
| dc.format.mimetype | application/pdf | es |
| dc.language.iso | spa | es |
| dc.publisher | The Royal Society of Chemistry | es |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | es |
| dc.title | Synthesis of chiral α-alkynyl-α-hydroxyamides by enantioselective alkynylation of α-keto amides | es |
| dc.type | info:eu-repo/semantics/article | es |
| dc.identifier.doi | 10.1039/d5ob01546d | es |
| dc.identifier.publicationfirstpage | 10596 | es |
| dc.identifier.publicationissue | 46 | es |
| dc.identifier.publicationlastpage | 10605 | es |
| dc.identifier.publicationtitle | Organic & Biomolecular Chemistry | es |
| dc.identifier.publicationvolume | 23 | es |
| dc.peerreviewed | SI | es |
| dc.description.project | Junta de Castilla y León (projects FEDER-VA115P17 and VA149G18) | es |
| dc.identifier.essn | 1477-0539 | es |
| dc.type.hasVersion | info:eu-repo/semantics/publishedVersion | es |



