Utilize este identificador para referenciar este registo:
http://hdl.handle.net/10362/150333Registo completo
| Campo DC | Valor | Idioma |
|---|---|---|
| dc.contributor.author | Santos, A. Sofia | - |
| dc.contributor.author | Ferro, Rita D. | - |
| dc.contributor.author | Viduedo, Nuno | - |
| dc.contributor.author | Maia, Luísa B. | - |
| dc.contributor.author | Silva, Artur M. S. | - |
| dc.contributor.author | Marques, M. Manuel B. | - |
| dc.date.accessioned | 2023-03-10T22:51:11Z | - |
| dc.date.available | 2023-03-10T22:51:11Z | - |
| dc.date.issued | 2023-01 | - |
| dc.identifier.issn | 2191-1363 | - |
| dc.identifier.other | PURE: 50901166 | - |
| dc.identifier.other | PURE UUID: 3d1305e4-1b4f-4f8a-a9b5-3b2c839c39dd | - |
| dc.identifier.other | Scopus: 85146409622 | - |
| dc.identifier.other | WOS: 000920124000001 | - |
| dc.identifier.other | PubMed: 36650736 | - |
| dc.identifier.other | PubMedCentral: PMC9845755 | - |
| dc.identifier.other | ORCID: /0000-0002-6712-752X/work/130607384 | - |
| dc.identifier.other | ORCID: /0000-0002-6901-6591/work/130607439 | - |
| dc.identifier.uri | http://hdl.handle.net/10362/150333 | - |
| dc.description | The National NMR Facility is supported by FCT, ROTEIRO/0031/2013-PINFRA/22161/2016, co-financed by FEDER through COMPETE2020, POCI, and PORLandFCT through PIDDAC) and CERMAX(022162). | - |
| dc.description.abstract | The indole moiety is an important N-heterocycle found in natural products, and a key structural component of many value-added chemicals including pharmaceuticals. In particular, bis(3-indolyl)methanes (BIMs) are an important subgroup of indoles, composed of two indole units. Herein, we report the development of a simple method to access BIMs derivatives in yields of up to 77 % by exploiting a tBuOK-mediated coupling reaction of indoles and benzyl alcohols. | en |
| dc.format.extent | 7 | - |
| dc.language.iso | eng | - |
| dc.relation | info:eu-repo/grantAgreement/FCT//PD%2FBD%2F142876%2F2018/PT | - |
| dc.relation | info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50006%2F2020/PT | - |
| dc.relation | info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50006%2F2020/PT | - |
| dc.relation | info:eu-repo/grantAgreement/FCT/CEEC IND 2017/CEECIND%2F03810%2F2017%2FCP1462%2FCT0017/PT | - |
| dc.rights | openAccess | - |
| dc.subject | bis(indolyl)methanes | - |
| dc.subject | indole | - |
| dc.subject | tBuOK | - |
| dc.subject | radicals | - |
| dc.subject | benzylalcohols | - |
| dc.subject | Chemistry(all) | - |
| dc.title | Synthesis of Bis(3-indolyl)methanes Mediated by Potassium tert-Butoxide | - |
| dc.type | article | - |
| degois.publication.issue | 1 | - |
| degois.publication.title | ChemistryOpen | - |
| degois.publication.volume | 12 | - |
| dc.peerreviewed | yes | - |
| dc.identifier.doi | https://doi.org/10.1002/open.202200265 | - |
| dc.description.version | publishersversion | - |
| dc.description.version | published | - |
| dc.contributor.institution | LAQV@REQUIMTE | - |
| dc.contributor.institution | DQ - Departamento de Química | - |
| Aparece nas colecções: | Home collection (FCT) | |
Ficheiros deste registo:
| Ficheiro | Descrição | Tamanho | Formato | |
|---|---|---|---|---|
| Synthesis_of_Bis_3_indolyl_methanes_Mediated_by_Potassium_tert_Butoxide.pdf | 4,35 MB | Adobe PDF | Ver/Abrir |
Todos os registos no repositório estão protegidos por leis de copyright, com todos os direitos reservados.











