Preparación de un plausible eje de rotaxano quiral aminoácido-esteroide

dc.contributor.authorCorona Sánchez, Ricardo
dc.contributor.authorGutiérrez Carrillo, Atilano
dc.contributor.authorGarcía Martínez, Cirilo
dc.contributor.authorSantillán Baca, Rosa Luisa
dc.contributor.authorSánchez Eleuterio, Alma
dc.creatorCORONA SANCHEZ, RICARDO; 257127
dc.creatorGUTIERREZ CARRILLO, ATILANO; 504192
dc.creatorGARCIA MARTINEZ, CIRILO; 9806
dc.creatorSANTILLAN BACA, ROSA LUISA; 280
dc.creatorSANCHEZ ELEUTERIO, ALMA; 257189
dc.date.accessioned2023-01-24T18:01:41Z
dc.date.available2023-01-24T18:01:41Z
dc.date.issued2021
dc.description.abstractRotaxanes are compounds that are made up of two submolecular components: a cyclic one (a ring) and a linear one (an axis) that threads the previous one and that, in addition, has bulky groups at their ends in order to keep both components intertwined. Another simple tool to keep this type of macrostructures anchored is through non-covalent bonds such as hydrogen bonds, coordination bonds with metal ions and aromatic π-π interactions, among others. In this work the rapid and quantitative synthesis of a conductive thread (chiral axis) composed of chiral molecules is reported, which give it excellent anchoring properties important for the synthesis of rotaxanes.es_MX
dc.description.abstractRotaxanes are compounds that are made up of two submolecular components: a cyclic one (a ring) and a linear one (an axis) that threads the previous one and that, in addition, has bulky groups at their ends in order to keep both components intertwined. Another simple tool to keep this type of macrostructures anchored is through non-covalent bonds such as hydrogen bonds, coordination bonds with metal ions and aromatic π-π interactions, among others. In this work the rapid and quantitative synthesis of a conductive thread (chiral axis) composed of chiral molecules is reported, which give it excellent anchoring properties important for the synthesis of rotaxanes.
dc.formatpdfes_MX
dc.identificator2||23||2306||330305es_MX
dc.identifier.urihttps://hdl.handle.net/11191/9331
dc.language.isospaes_MX
dc.publisherUniversidad Autónoma Metropolitana (México). Unidad Azcapotzalco. División de Ciencias Básicas e Ingeniería.es_MX
dc.rightsAtribución-NoComercial-SinDerivadas
dc.rights.accesopenAccesses_MX
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0
dc.sourceRevista Tendencias en Docencia e Investigación en Química. Año 7, número 7 (enero-diciembre de 2021). ISSN: 2448-6663
dc.subjectRotaxano, aminoa cido, esteroide. Rotaxane, aminoacid, steroid.es_MX
dc.subject.classificationBIOLOGÍA Y QUÍMICA::QUÍMICA::QUÍMICA ORGÁNICA::SÍNTESIS QUÍMICAes_MX
dc.titlePreparación de un plausible eje de rotaxano quiral aminoácido-esteroidees_MX
dc.typeArtículoes_MX
dc.type.conacytarticle

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Preparación de un plausible eje de rotaxano