| dc.contributor.author | Netz, Natalie | |
| dc.contributor.author | Díez Poza, Carlos | |
| dc.contributor.author | Barbero Pérez, María Asunción | |
| dc.contributor.author | Opatz, Till | |
| dc.date.accessioned | 2025-01-28T12:29:36Z | |
| dc.date.available | 2025-01-28T12:29:36Z | |
| dc.date.issued | 2017 | |
| dc.identifier.citation | European Journal of Organic Chemistry, 2017(31), 4580-4599. | es |
| dc.identifier.issn | 1434-193X | es |
| dc.identifier.uri | https://uvadoc.uva.es/handle/10324/74514 | |
| dc.description.abstract | A modular synthesis of unsymmetrical BODIPY dyes
based on a [6π] electrocyclization to construct both pyrrole
rings is presented. The products carry four aryl moieties in positions
1, 3, 5, and 7, which can be freely selected, as well as optional substitution in positions 2 and 8. The method employs acetophenones, benzaldehydes as well as glycine nitrile or
glycine ethyl ester as the key building blocks. | es |
| dc.format.mimetype | application/pdf | es |
| dc.language.iso | eng | es |
| dc.publisher | John Wiley & Sons, Inc | es |
| dc.rights.accessRights | info:eu-repo/semantics/restrictedAccess | es |
| dc.title | Modular De novo Synthesis of Unsymmetrical BODIPY Dyes Possessing Four Different Aryl Substituents | es |
| dc.type | info:eu-repo/semantics/article | es |
| dc.rights.holder | John Wiley & Sons, Inc | es |
| dc.identifier.doi | 10.1002/EJOC.201700773 | es |
| dc.relation.publisherversion | https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201700773 | es |
| dc.identifier.publicationfirstpage | 4580 | es |
| dc.identifier.publicationissue | 31 | es |
| dc.identifier.publicationlastpage | 4599 | es |
| dc.identifier.publicationtitle | European Journal of Organic Chemistry | es |
| dc.identifier.publicationvolume | 2017 | es |
| dc.peerreviewed | SI | es |
| dc.identifier.essn | 1099-0690 | es |
| dc.type.hasVersion | info:eu-repo/semantics/publishedVersion | es |
