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Enantioselective synthesis of a two-fold inherently chiral molecular nanographene

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dc.contributor.affiliation000000041762408X
dc.contributor.affiliation"Departamento de Química Orgánica I, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n, Madrid, Spain"," Laboratorio DRX Monocristal, SIdI, Universidad Autónoma de Madrid, Madrid, Spain"," IMDEA-Nanociencia, Campus de Cantoblanco, Madrid, Spain"en
dc.contributor.authorBuendía M.
dc.contributor.authorFernández-García J.M.
dc.contributor.authorPerles J.
dc.contributor.authorFilippone S.
dc.contributor.authorMartín, Nazario
dc.date.accessioned2024-04-19T10:03:59Z
dc.date.available2024-04-19T10:03:59Z
dc.date.issued2024
dc.format.mimetypeapplication/pdfen
dc.identifier.doi10.1038/s44160-024-00484-xen
dc.identifier.urihttps://hdl.handle.net/20.500.12614/3636
dc.journal.titleNature Synthesisen
dc.language.isoenen
dc.relation.projectIDTEMPM.B., S.F., J.M.F.-G. and N.M. acknowledge financial support from the Spanish MICIN (project PID2020-114653RB-I00), they also acknowledge financial support from the ERC (SyG TOMATTO ERC-2020-951224) and from the ‘(MAD2D-CM)-UCM’ project funded by Comunidad de Madrid, by the Recovery, Transformation and Resilience Plan and by NextGenerationEU from the European Union. M.B. also acknowledges financial support from the Spanish MICIN (project CTQ2017-83531-R). J.P. thanks M. Ramírez and P. Martínez-Martín for their help with the molecular models. We also acknowledge L. Favereau for his help in the CPL measurements at Rennes Institute of Chemical Sciences, Rennes, France.
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.accessRightsopen accessen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.titleEnantioselective synthesis of a two-fold inherently chiral molecular nanographeneen
dc.typeresearch articleen
dc.type.hasVersionVoRen
dspace.entity.typePublication

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