Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Adrian Saura-Sanmartin"'
Autor:
Adrian Saura-Sanmartin
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 873-880 (2023)
Light-responsive rotaxane-based solid-state materials are ideal scaffolds in order to develop smart materials due to the properties provided by the mechanical bond, such as control over the dynamics of the components upon application of external stim
Externí odkaz:
https://doaj.org/article/2dc1195082a7409aae1b26bc45f0e992
Autor:
Antonio Garcia-Jimenez, Jose Antonio Teruel-Puche, Pedro Antonio Garcia-Ruiz, Adrian Saura-Sanmartin, Jose Berna, Francisco Garcia-Canovas, José Neptuno Rodriguez-Lopez
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0187845 (2017)
Deoxyarbutin, a potent inhibitor of tyrosinase, could act as substrate of the enzyme. Oxytyrosinase is able to hydroxylate deoxyarbutin and finishes the catalytic cycle by oxidizing the formed o-diphenol to quinone, while the enzyme becomes deoxytyro
Externí odkaz:
https://doaj.org/article/4755ebd5057f47cf930552c565b3b6ca
Publikováno v:
Supramolecular Nanotechnology. :515-537
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b5482a34ef055a13eeb6ad84445be2b
https://doi.org/10.1002/9783527834044.ch19
https://doi.org/10.1002/9783527834044.ch19
Publikováno v:
Chem. 9:823-846
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32b9fcc63340880dc866eb5b9175f31a
https://doi.org/10.1016/j.chempr.2023.03.015
https://doi.org/10.1016/j.chempr.2023.03.015
Publikováno v:
Organic & Biomolecular Chemistry. 21:3296-3306
This review covers recent advances towards the stereoselective synthesis of β-lactam derivatives, which is a research topic of great interest due to the biological activity of these molecules.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f1ebc74daebcc0bd3f8190aae31a759
https://doi.org/10.1039/d3ob00309d
https://doi.org/10.1039/d3ob00309d
Autor:
Adrian Saura-Sanmartin, Tomas Nicolas-Garcia, Aurelia Pastor, David Quiñonero, Mateo Alajarin, Alberto Martinez-Cuezva, Jose Berna
Publikováno v:
Chemical Science. 14:4143-4151
The self-association of a ditopic [2]rotaxane with two macrocycles mainly leads to a [4]pseudorotaxane which can be reversibly disassembled by adding competitive binders, varying the solvent polarity and changing a binding site affinity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ae9b90fc6cb8645932152b512cd40dd
https://doi.org/10.1039/d3sc00886j
https://doi.org/10.1039/d3sc00886j
Autor:
Mateo Alajarin, Jose Berna, Adrian Saura-Sanmartin, Guillermo Cutillas-Font, Aurelia Pastor, Alberto Martinez Cuezva
Publikováno v:
Chemical Society Reviews. 51:4949-4976
Mechanically interlocked molecules (MIMs) have great potential in the development of molecular machinery due to their intercomponent dynamics. The incorporation of these molecules in a condensed phase makes it possible to take advantage of the contro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::441a00097ac05733ad3c7f0fb7109841
https://doi.org/10.1039/d2cs00167e
https://doi.org/10.1039/d2cs00167e
Maximizing the [c2]daisy chain to lasso ratio through competitive self-templating clipping reactions
Publikováno v:
Chemical Communications. 58:290-293
Single versus double self-templating clipping reactions allow the preparation of amide-based lasso and [c2]daisy chain rotaxanes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8be75bcb75a9e571c76569c829f00218
https://doi.org/10.1039/d1cc05942d
https://doi.org/10.1039/d1cc05942d
Publikováno v:
Israel Journal of Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2615eb3dd601c421e68e8820b711adc0
https://doi.org/10.1002/ijch.202300022
https://doi.org/10.1002/ijch.202300022
Autor:
Adrian Saura-Sanmartin
Publikováno v:
European Journal of Organic Chemistry. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c72a8a72bd7a729893a727dc2e4e1f1
https://doi.org/10.1002/ejoc.202201512
https://doi.org/10.1002/ejoc.202201512