Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ferran Esteve"'
Autor:
Julián E. Sánchez-Velandia, Ferran Esteve, Miguel Maireles, Diego Iglesias, Nuria Martín, Marcileia Zanatta, Victor Sans, Francisco G. Cirujano, Eduardo García-Verdugo
Publikováno v:
Journal of CO2 Utilization, Vol 78, Iss , Pp 102636- (2023)
A novel approach is reported to prepare 3D-printed polymers that incorporate metal-organic frameworks (MOFs) through a one-pot growth process, involving covalent grafting and growth onto 3D polymeric surfaces. The resulting hybrid materials were subj
Externí odkaz:
https://doaj.org/article/a57e6f5ae98b494480360fdbd3c0e05f
Autor:
Ferran Esteve, Alexis Villanueva-Antolí, Belén Altava, Eduardo García-Verdugo, Santiago V. Luis
Publikováno v:
Gels, Vol 8, Iss 6, p 390 (2022)
A new family of C2-symmetric pseudopeptides with a high functional density for supramolecular interactions has been synthetized through the attachment of four amino acid subunits to a diamino aliphatic spacer. The resulting open-chain compounds prese
Externí odkaz:
https://doaj.org/article/e749f7f90c4648de926b7d13f47e37e6
Publikováno v:
Organicbiomolecular chemistry. 20(33)
The reaction mechanism for the cycloaddition of CO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b19c76bfba5d69fc781376df52f1d81f
https://pubmed.ncbi.nlm.nih.gov/35929502
https://pubmed.ncbi.nlm.nih.gov/35929502
Autor:
Ferran Esteve, Raúl Porcar, Michael Bolte, Belén Altava, Santiago V. Luis, Eduardo García-Verdugo
Publikováno v:
Chem Catalysis. 3:100482
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf04dca08560006766fe625b9eddc1e0
https://doi.org/10.1016/j.checat.2022.11.021
https://doi.org/10.1016/j.checat.2022.11.021
Publikováno v:
Repositori Universitat Jaume I
Universitat Jaume I
Universitat Jaume I
Taking advantage of the dynamic covalent chemistry approach, four different cages were synthesized by condensation of tripodal pseudopeptides with 4,4′-biphenyldicarboxyaldehyde. Whereas undesired products of polymeric nature were obtained in polar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4628720c4eeb3e2a522cf7820c63d731
Autor:
Eduardo Garcia-Verdugo, Alexis Villanueva Antoli, Santiago V. Luis, Belen Altava, Ferran Esteve Franch
Publikováno v:
Gels; Volume 8; Issue 6; Pages: 390
Repositori Universitat Jaume I
Universitat Jaume I
Repositori Universitat Jaume I
Universitat Jaume I
A new family of C2 -symmetric pseudopeptides with a high functional density for supramolecular interactions has been synthetized through the attachment of four amino acid subunits to a diamino aliphatic spacer. The resulting open-chain compounds pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82005707a65d33a980db426103625a93
Autor:
Eduardo García-Verdugo, M. Isabel Burguete, Santiago V. Luis, Michael Bolte, Ferran Esteve, Belén Altava
Publikováno v:
Green Chemistry. 22:4697-4705
A series of pseudopeptidic compounds have been assayed as organocatalyts for the conversion of CO2 into organic carbonates through a cooperative multifunctional mechanism. Conformationally constrained pseudopeptidic macrocycles 3a and 3b have been re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7350889bea55721e40ebe6becf6c9fb9
https://doi.org/10.1039/d0gc01449d
https://doi.org/10.1039/d0gc01449d
Autor:
Ferran Esteve, Adrian Escrig, Raul Porcar, Santiago V. Luis, Belén Altava, Eduardo García‐Verdugo
Publikováno v:
Advanced Sustainable Systems. 6:2100408
Supramolecular catalysis can provide distinct advantages for the catalytic conversion of CO2 into carbonates by cycloaddition to epoxides. For example, the absence of metals in the catalytic site, and the easy design for optimization. The incorporati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afe666a5a1bccef7f58e325859579cc7
https://doi.org/10.1002/adsu.202100408
https://doi.org/10.1002/adsu.202100408
Autor:
M. Isabel Burguete, Belén Altava, Ferran Esteve, Michael Bolte, Eduardo García-Verdugo, Santiago V. Luis
Publikováno v:
Repositori Universitat Jaume I
Universitat Jaume I
Universitat Jaume I
Herein, we report the synthesis of a novel family of constrained pseudopeptidic macrocyclic compounds containing the hexahydropyrrolo[3,4-f]isoindolocyclophane scaffold and involving four coupled substitution reactions in the macrocyclization process
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38dfd95132d3c05865b6266dda03987b