Please use this identifier to cite or link to this item:
http://hdl.handle.net/10662/22099
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Bornadiego Suárez, Ana | - |
dc.contributor.author | Gómez Neo, Ana María | - |
dc.contributor.author | Fernández Marcos, Carlos María | - |
dc.date.accessioned | 2024-08-27T09:57:38Z | - |
dc.date.available | 2024-08-27T09:57:38Z | - |
dc.date.issued | 2021 | - |
dc.identifier.uri | http://hdl.handle.net/10662/22099 | - |
dc.description.abstract | Keto piperazines and aminocoumarins are privileged building blocks for the construction of geometrically constrained peptides and therefore valuable structures in drug discovery. Combining these two heterocycles provides unique rigid polycyclic peptidomimetics with drug-like properties including many points of diversity that could be modulated to interact with different biological receptors. This work describes an efficient multicomponent approach to condensed chromenopiperazines based on the novel enol-Ugi reaction. Importantly, this strategy involves the first reported post-condensation transformation of an enol-Ugi adduct. | es_ES |
dc.description.sponsorship | This research was funded by Junta de Extremadura and FEDER (IB16095) | es_ES |
dc.format.extent | 18 p. | es_ES |
dc.format.mimetype | application/pdf | en_US |
dc.language.iso | eng | es_ES |
dc.publisher | MDPI | es_ES |
dc.rights | Attribution 4.0 International | * |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject | Reacciones multicomponentes | es_ES |
dc.subject | Isocianuros | es_ES |
dc.subject | Peptidomimético | es_ES |
dc.subject | Heterociclos | es_ES |
dc.subject | Piperazinas | es_ES |
dc.subject | Pirazinas | es_ES |
dc.subject | Cromonas | es_ES |
dc.subject | Cumarinas | es_ES |
dc.subject | Enoles | es_ES |
dc.subject | Reacción de Ugi | es_ES |
dc.subject | Imulticomponent reactions | es_ES |
dc.subject | Peptidomimetics | es_ES |
dc.subject | isocyanides | es_ES |
dc.subject | Heterocycles | es_ES |
dc.subject | Piperazines | es_ES |
dc.subject | Chromones | es_ES |
dc.subject | Coumarins | es_ES |
dc.subject | Enols | es_ES |
dc.subject | Ugi reaction | es_ES |
dc.title | Synthesis of Chromeno[3,4-b]piperazines by an Enol-Ugi/Reduction/Cyclization Sequence | es_ES |
dc.type | article | es_ES |
dc.description.version | peerReviewed | es_ES |
europeana.type | TEXT | en_US |
dc.rights.accessRights | openAccess | es_ES |
dc.subject.unesco | 2302 Bioquímica | es_ES |
dc.subject.unesco | 2302.24-1 Síntesis de Péptidos | es_ES |
dc.subject.unesco | 2304.18 Polipéptidos y Proteínas | es_ES |
europeana.dataProvider | Universidad de Extremadura. España | es_ES |
dc.identifier.bibliographicCitation | Bornadiego, A.;Neo, A. G.; Marcos, C. F., Synthesis of chromeno[3,4-b]piperazines by an enol-Ugi/reduction/cyclization sequence. Molecules 2021, 26 (5), 1287. doi: http://dx.doi.org/10.3390/molecules26051287 | es_ES |
dc.type.version | publishedVersion | es_ES |
dc.contributor.affiliation | Universidad de Extremadura. Departamento de Química Orgánica e Inorgánica | es_ES |
dc.relation.publisherversion | https://www.mdpi.com/1420-3049/26/5/1287 | es_ES |
dc.identifier.doi | 10.3390/molecules26051287 | - |
dc.identifier.publicationtitle | Molecules | es_ES |
dc.identifier.publicationissue | 5 | es_ES |
dc.identifier.publicationfirstpage | 1287-1 | es_ES |
dc.identifier.publicationlastpage | 1287-18 | es_ES |
dc.identifier.publicationvolume | 26 | es_ES |
dc.identifier.e-issn | 1420-3049 | - |
dc.identifier.orcid | 0000-0002-9755-096X | es_ES |
dc.identifier.orcid | 0000-0003-2149-1489 | es_ES |
dc.identifier.orcid | 0000-0003-2278-7118 | es_ES |
Appears in Collections: | DQOIN - Artículos |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
molecules26051287.pdf | 868,45 kB | Adobe PDF | View/Open |
This item is licensed under a Creative Commons License