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Process Intensification for the Synthesis of 6-Allyl-6-azabicyclo[3.1.0]hex-3-en-2-ol from 1-Allylpyridinium Salt Using a Continuous UV-Light Photoflow Approach

dc.contributor.authorFortunato, Milene
dc.contributor.authorLy, Chi-Phong
dc.contributor.authorSiopa, Filipa
dc.contributor.authorAfonso, Carlos
dc.date.accessioned2023-09-14T14:52:15Z
dc.date.available2023-09-14T14:52:15Z
dc.date.issued2019-08-05
dc.date.updated2023-02-23T10:55:44Z
dc.description© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).pt_PT
dc.description.abstractA new home-made UV photochemical reactor (95 cm of irradiation zone) consisting of a 12 parallel quartz tubes flow reactor, PQT6 (95 cm under irradiation and an internal diameter of 0.6 cm) was assembled to perform photochemical transformations in continuous-flow. PQT6 was evaluated for the photoreaction of 1-allylpyridinium bromide (1a) to 6-allyl-6-azabicyclo[3.1.0]hex-3-en-2-ol (2a), in a continuous process. This technology provides reduced reaction times, continuous production of 2a, and a productivity of 129 mg h−1, corresponding to 1.94 g of isolated 2a after 15 h of irradiation.pt_PT
dc.description.sponsorshipThis research was funded by Fundação para a Ciência e a Tecnologia (FCT) (ref. PTDC/QUI-QOR/32008/2017, UID/DTP/04138/2013, PESSOA 2018/2019 (Proc. 441.00 França and PHC PESSOA 2018 No 40875QJ)) and European Research Area Network; ERANet LAC (ref. ELAC2014/BEE-0341).pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationFortunato MAG, Ly C-P, Siopa F, Afonso CAM. Process Intensification for the Synthesis of 6-Allyl-6-azabicyclo[3.1.0]hex-3-en-2-ol from 1-Allylpyridinium Salt Using a Continuous UV-Light Photoflow Approach. Methods and Protocols [Internet]. 2019 Aug 5;2(3):67. Available from: http://dx.doi.org/10.3390/mps2030067pt_PT
dc.identifier.doi10.3390/mps2030067pt_PT
dc.identifier.slugcv-prod-1102369
dc.identifier.urihttp://hdl.handle.net/10451/59299
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMDPIpt_PT
dc.relationPTDC/QUI-QOR/32008/2017pt_PT
dc.relationUID/DTP/04138/2013pt_PT
dc.relation.publisherversionhttps://www.mdpi.com/2409-9279/2/3/67pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectflow reactionpt_PT
dc.subjectphotochemistrypt_PT
dc.subjectbicyclic aziridinept_PT
dc.titleProcess Intensification for the Synthesis of 6-Allyl-6-azabicyclo[3.1.0]hex-3-en-2-ol from 1-Allylpyridinium Salt Using a Continuous UV-Light Photoflow Approachpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue3pt_PT
oaire.citation.startPage67pt_PT
oaire.citation.titleMethods and Protocolspt_PT
oaire.citation.volume2pt_PT
person.familyNameGamito Fortunato
person.familyNameDeslgado Siopa
person.familyNameMateus Afonso
person.givenNameMilene Andreia
person.givenNameFilipa Alexandra
person.givenNameCarlos Alberto
person.identifier.ciencia-idAA16-A885-3ABD
person.identifier.ciencia-id6A16-150F-A9F9
person.identifier.ciencia-id6319-2E4C-5BE1
person.identifier.orcid0000-0003-1072-0709
person.identifier.orcid0000-0002-4514-9154
person.identifier.orcid0000-0002-7284-5948
rcaap.cv.cienciaid6A16-150F-A9F9 | Filipa Alexandra Delgado Siopa
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationfd831776-6563-41ed-b777-1cec2703f955
relation.isAuthorOfPublicationa64b1654-ee75-40fa-b039-b9829c65af3a
relation.isAuthorOfPublication811958c9-3280-45c4-bff2-dd54318875d0
relation.isAuthorOfPublication.latestForDiscovery811958c9-3280-45c4-bff2-dd54318875d0

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