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Transformant un programa de formació inicial docent amb tecnologies mòbils. Una síntesi d'evidències qualitatives

Autor: Ngao, Ayubu, Sang, Guoyuan, Tondeur, Jo, Kihwele, Jimmy Ezekiel, Chunga, Jasmin Omary

Publikováno v: Digital Education Review; No 43 (2023): Number 43, June 2023; 18-36
Digital Education Review; No. 43 (2023): Number 43, June 2023; 18-36
Digital Education Review; Núm. 43 (2023): Number 43, June 2023; 18-36

Les tecnologies mòbils s'han utilitzat cada cop més en l'educació per millorar l'ensenyament i l'aprenentatge entre els estudiants. Els autors han revisat estudis qualitatius que se centraven en enfocaments per transformar els programes de formaci

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=rcubrevistes::5477cef2390f232a27e0ef0c439efc8b
http://revistes.ub.edu/index.php/der/article/view/40243

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Synthesis of antivirals applying Green Chemistry principles

Autor: Flix Rubio, Laia

Treballs Finals de Grau de Química, Facultat de Química, Universitat de Barcelona, Any: 2023, Tutor: Jordi Robles Brau
Green chemistry aims at reducing and eliminating the use or generation of hazardous substances by designing alternative rout

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______963::7208c7b32c9e066740b4144a619c3af1
http://hdl.handle.net/2445/200629

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Enantioselective carbon-carbon bond forming reactions catalyzed by chiral nickel (II) complexes

Autor: Lamrhari Elabiad, Otman

Treballs Finals de Grau de Química, Facultat de Química, Universitat de Barcelona, Any: 2023, Tutor: Pedro Romea García
Over the past decades, the construction of new carbon-carbon bonds has been of great importance in the synthesis of organi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______963::636aa7ecc966bd2261da531bc3836ea7
http://hdl.handle.net/2445/200672

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In Silico Identification and Experimental Validation of Distal Activity-Enhancing Mutations in Tryptophan Synthase

Autor: Miguel A. Maria-Solano, Thomas Kinateder, Reinhard Sterner, Sílvia Osuna, Javier Iglesias-Fernández

Publikováno v: ACS Catalysis
ACS Catalysis, 2021, vol. 11, núm. 21, p. 13733-13743
Articles publicats (D-Q)
DUGiDocs – Universitat de Girona
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Allostery is a central mechanism for the regulation of multi-enzyme complexes. The mechanistic basis that drives allosteric regulation is poorly understood but harbors key information for enzyme engineering. In the present study, we focus on the tryp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::282f8a60b04a6ec15909e4b11a6738e4
http://europepmc.org/articles/PMC8576815

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Designing Advanced Nanocatalysts: Synthesis of complex CeO2-based Nanostructures

Autor: Hervés Carrete, Carmen

[eng] The main objective of this dissertation has been to stablish a bridge between materials science and its fields of application. The scope of this thesis work, under this premise, is aimed towards understanding the catalytical properties of CeO2

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______963::ef150a4e6b62d0f38dd0ee2489ea6327
http://hdl.handle.net/10803/688442

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Trioleyl Pyridinium, a Cationic Transfection Agent for the Lipofection of Therapeutic Oligonucleotides into Mammalian Cells

Autor: Ana Delgado, Rosa Griera, Núria Llor, Ester López-Aguilar, Maria Antònia Busquets, Véronique Noé, Carlos J. Ciudad

Publikováno v: Pharmaceutics
Volume 15
Issue 2
Pages: 420

Background: One of the most significant limitations that therapeutic oligonucleotides present is the development of specific and efficient delivery vectors for the internalization of nucleic acids into cells. Therefore, there is a need for the develo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14f9c2fa0a6cb7badb0f9f67790a4eec
http://hdl.handle.net/2445/194009

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Synthesis of oligonucleotide-based RNase H1-sensitive structures: a strategy with potential in breast cancer therapy and nanotechnology

Autor: Torrents Lara, Maria

Treballs Finals de Grau de Química, Facultat de Química, Universitat de Barcelona, Any: 2023, Tutora: Montserrat Terrazas Martinez
The rising number of drug resistance cases, as well as untreatable illnesses by current approved therapies has e

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______963::0352f9e82660a578e622874c00457b44
http://hdl.handle.net/2445/195005

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Synthesis of lead-free iodide perovskites

Autor: Casas Comas, Carlota

Treballs Finals de Grau de Química, Facultat de Química, Universitat de Barcelona, Any: 2023, Tutor: Roc Matheu Montserrat
Lead halide perovskites are developed for light-absorbing applications (e.g., solar cells), but concerns about the toxic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______963::cd0c7ef197acd73c407bfa2676c38bb1
http://hdl.handle.net/2445/195042

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Direct and Asymmetric Aldol Reactions of N-Azidoacetyl-1,3-thiazolidine-2-thione Catalyzed by Chiral Nickel(II) Complexes. A New Approach to the Synthesis of -Hydroxy--Amino Acids

Autor: Saul F. Teloxa, Miguel Mellado‐Hidalgo, Stuart C. D. Kennington, Pedro Romea, Fèlix Urpí, Gabriel Aullón, Mercè Font‐Bardia

A direct and asymmetric triisopropylsilyltrifluoromethanesulfonate (TIPSOTf) mediated aldol reaction of N-azidoacetyl-1,3-thiazolidine-2-thione with aromatic aldehydes catalyzed by a chiral nickel(II)-Tol-BINAP complex has been developed (BINAP=2,2'-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::630c027506f0f863305bc0fc27aeb5a7
http://hdl.handle.net/2445/191586

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Synthesis and Acylation of 1,3-Thiazinane-2-thione

Autor: Kennington, Stuart C. D., Galeote, Oriol, Mellado Hidalgo, Miquel, Romea, Pedro, Urpí Tubella, Fèlix

Publikováno v: Dipòsit Digital de la UB
Universidad de Barcelona

1. Procedure (Note 1) A. 3-Ammoniopropylsulfate (1). An oven-dried single-necked 100 mL round-bottomed flask (14/23 joint), equipped with a 2.5-cm Teflon-coated magnetic stirbar, is charged with 3-amino-1-propanol (11.5 mL, 150 mmol, 1 equiv) (Note 2

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b245fd99cd7b55bc820ed4bee189ffe4
https://doi.org/10.15227/orgsyn.098.0374

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