Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Vanesa Marcos"'
Autor:
Vanesa MARCOS SÁNCHEZ
Publikováno v:
Teoría de la Educación: Educación y Cultura en la Sociedad de la Información, Vol 13, Iss 1, Pp 485-487 (2012)
Externí odkaz:
https://doaj.org/article/de9d3342c518411ea245ab485e3598f2
Autor:
Vanesa MARCOS SÁNCHEZ
Publikováno v:
Education in the Knowledge Society, Vol 13, Iss 1, Pp 485-487 (2012)
Externí odkaz:
https://doaj.org/article/6a359520d1cf4dd5ad89fa54eddbbfbb
Autor:
Vanesa Marcos Sánchez
Publikováno v:
Teoría de la Educación: Educación y Cultura en la Sociedad de la Información, Vol 12, Iss 1, Pp 417-418 (2011)
Externí odkaz:
https://doaj.org/article/130c4383a42b4d1b99494d0e799a9905
Autor:
Javier Echavarren, Adrian Haertsch, Malcolm A. Y. Gall, Vanesa Marcos, Daniel J. Tetlow, David A. Leigh
Publikováno v:
Chemical Science
Echavarren, J, Gall, M A Y, Haertsch, A, Leigh, D A, Marcos, V & Tetlow, D J 2019, ' Active template rotaxane synthesis through the Ni-catalyzed cross-coupling of alkylzinc reagents with redox-active esters ', Chemical Science, vol. 10, no. 30, pp. 7269-7273 . https://doi.org/10.1039/c9sc02457c
Echavarren, J, Gall, M A Y, Haertsch, A, Leigh, D A, Marcos, V & Tetlow, D J 2019, ' Active template rotaxane synthesis through the Ni-catalyzed cross-coupling of alkylzinc reagents with redox-active esters ', Chemical Science, vol. 10, no. 30, pp. 7269-7273 . https://doi.org/10.1039/c9sc02457c
The Ni-catalyzed C(sp3)–C(sp3) cross-coupling of redox-active esters and organozinc reagents is used for the active template synthesis of ‘impossible’ rotaxanes.
The synthesis of unsymmetrical axle [2]rotaxanes through a recently developed
The synthesis of unsymmetrical axle [2]rotaxanes through a recently developed
Publikováno v:
Zhang, L, Marcos Algaba, V & Leigh, D 2018, ' Molecular Machines with Bio-Inspired Mechanisms ', Proceedings of the National Academy of Sciences . https://doi.org/10.1073/pnas.1712788115
The widespread use of molecular-level motion in key natural processes suggests that great rewards could come from bridging the gap between the present generation of synthetic molecular machines—which by and large function as switches—and the mach
Autor:
Katarzyna Eichstaedt, Simone Pisano, Vanesa Marcos, Javier Jaramillo-Garcia, Thomas A. Singleton, David A. Leigh
Publikováno v:
Eichstaedt, K, Jaramillo Garca, J, Leigh, D, Marcos Algaba, V, Pisano, S & Singleton, T 2017, ' Switching Between Anion-Binding Catalysis and Aminocatalysis with a Rotaxane Dual-Function Catalyst ', Journal of the American Chemical Society . https://doi.org/10.1021/jacs.7b04955
The ‘off’ state for aminocatalysis by a switchable [2]rotaxane is shown to correspond to an ‘on’ state for anion-binding catalysis. Conversely, the aminocatalysis ‘on’ state of the dual-function rotaxane is inactive in anion-binding catal
Autor:
Iñigo J. Vitorica-Yrezabal, Xiaokang Zhu, Vanesa Marcos, David A. Leigh, Tugrul Nalbantoglu, F. Tuba Yasar
Publikováno v:
Leigh, D, Marcos Algaba, V, Nalbantoglu, T, Vitorica-Yrezabal, I, Tuba Yasar, F & Zhu, X 2017, ' Pyridyl-Acyl Hydrazone Rotaxanes and Molecular Shuttles ', Journal of the American Chemical Society, pp. 7104-7109 . https://doi.org/10.1021/jacs.7b03307
We report on rotaxanes featuring a pyridyl-acyl hydrazone moiety on the axle as a photo-/thermalswitchable macrocycle binding site. The pyridyl-acyl E-hydrazone acts as a hydrogen bonding template that directs the assembly of a benzylic amide macrocy
Publikováno v:
Angewandte Chemie International Edition
We report on a switchable rotaxane molecular shuttle that features a pseudo-meso 2,5-disubstituted pyrrolidine catalytic unit on the axle whose local symmetry is broken according to the position of a threaded benzylic amide macrocycle. The macrocycle
Publikováno v:
ACS Catalysis. 4:4490-4497
Publikováno v:
Kassem, S, Lee, A T L, Leigh, D, Marcos Algaba, V, Palmer, L & Pisano, S 2017, ' Stereodivergent synthesis with a programmable molecular machine ', Nature, vol. 549, pp. 374-378 . https://doi.org/10.1038/nature23677
It has been convincingly argued that molecular machines that manipulate individual atoms, or highly reactive clusters of atoms, with Angstrom precision are unlikely to be realized. However, biological molecular machines routinely position rather less
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b73d67346ed4ad5ac0f15e0b46b1621
https://pure.manchester.ac.uk/ws/files/59918499/AAM_22Sept2017_SynMolRobot_Nature.pdf
https://pure.manchester.ac.uk/ws/files/59918499/AAM_22Sept2017_SynMolRobot_Nature.pdf