Publication
Synthesis and transformation of halochromones
| dc.contributor.author | Tomé, Sara M. | |
| dc.contributor.author | Silva, Artur | |
| dc.contributor.author | Santos, Clementina M.M. | |
| dc.date.accessioned | 2015-03-02T10:31:20Z | |
| dc.date.available | 2015-03-02T10:31:20Z | |
| dc.date.issued | 2014 | |
| dc.description.abstract | Chromones (4H-1-benzopyran-4-ones) are one of the most abundant groups of naturally occurring oxygen containing heterocyclic compounds possessing a benzo-γ-pyrone framework, 1a. The significance of these widely spread and highly diverse compounds is far beyond the important biological functions they assume in nature [1, 2]. Natural and synthetic chromone derivatives have been assigned as lead structures in drug development with some already being marketed [3]. The majority of the naturally occurring chromones are 2- and 3-aryl derivatives, called flavones 1b and isoflavones 1c, respectively. However, other types of chromones have also been found in the plant kingdom, such as 3-methylchromones 1d and 2- styrylchromones 1e (Fig. 1). | por |
| dc.description.sponsorship | University of Aveiro, Fundação para a Ciência e a Tecnologia (FCT, Portugal), European Union, QREN, FEDER and COMPETE for funding the QOPNA Research Unit. | por |
| dc.identifier.citation | Tomé, Sara M.; Silva, Artur M.S.; Santos, Clementina M.M. (2014). Synthesis and transformation of halochromones. Current Organic Synthesis. ISSN 1570-1794. 11:3, p. 317-341 | por |
| dc.identifier.doi | 10.2174/15701794113109990063 | |
| dc.identifier.issn | 1570-1794 | |
| dc.identifier.uri | http://hdl.handle.net/10198/11714 | |
| dc.language.iso | eng | por |
| dc.peerreviewed | yes | por |
| dc.publisher | Bentham Science | por |
| dc.subject | Chromones | por |
| dc.subject | Cross-coupling reactions | por |
| dc.subject | Halochromones | por |
| dc.subject | Halogenation | por |
| dc.subject | Reactivity | por |
| dc.subject | Synthesis | por |
| dc.title | Synthesis and transformation of halochromones | por |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 341 | por |
| oaire.citation.startPage | 317 | por |
| oaire.citation.title | Curr. Org. Synth. | por |
| oaire.citation.volume | 11 | por |
| person.familyName | Santos | |
| person.givenName | Clementina M.M. | |
| person.identifier.ciencia-id | 9018-DB9C-C590 | |
| person.identifier.orcid | 0000-0003-4380-7990 | |
| person.identifier.scopus-author-id | 7201458663 | |
| rcaap.rights | openAccess | por |
| rcaap.type | article | por |
| relation.isAuthorOfPublication | 64f662b6-775d-4ea0-bfd7-f527af0ac1a0 | |
| relation.isAuthorOfPublication.latestForDiscovery | 64f662b6-775d-4ea0-bfd7-f527af0ac1a0 |