Zobrazeno 1 - 10
of 213
pro vyhledávání: '"Síntesi orgànica"'
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
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
http://hdl.handle.net/2445/200629
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
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
http://hdl.handle.net/2445/194009
Autor:
Bujaldón Carbó, Roger
[eng] The increasing demand on next-generation displays encourages an exhaustive research on the development of new and enhanced semiconductors. Apart from the conventional inorganic materials, organic-based semiconductors can also fulfil this role w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______963::522a6e4726e9bb0f14857bbf92de9cba
http://hdl.handle.net/2445/191640
http://hdl.handle.net/2445/191640
[spa] En el primer bloque de la tesis describimos nuestra aproximación a la síntesis total de la Palmerolida D, un compuesto de gran interés, tanto por sus propiedades antitumorales como por la diversidad de reacciones necesarias para llevar a cab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______963::bd87f145e9cc29ab00338a7a670bf24b
http://hdl.handle.net/2445/191371
http://hdl.handle.net/2445/191371
Autor:
Antonio Fernandez, Nicola Kielland, Ashraff Makda, Neil O. Carragher, M. Carmen González-García, Laura Espinar-Barranco, Juan A. González-Vera, Angel Orte, Rodolfo Lavilla, Marc Vendrell
Publikováno v:
Fernandez, A, Kielland, N, Makda, A, Carragher, N O, González-garcía, M C, Espinar-barranco, L, González-vera, J A, Orte, A, Lavilla, R & Vendrell, M 2022, ' A multicomponent reaction platform towards multimodal near-infrared BODIPY dyes for STED and fluorescence lifetime imaging ', RSC Chemical Biology . https://doi.org/10.1039/D2CB00168C
RSC Chemical Biology
RSC Chemical Biology
We report a platform combining multicomponent reaction synthesis and automated cell-based screening to develop biocompatible NIR-BODIPY fluorophores. From a library of over 60 fluorophores, we optimised compound NIRBD-62c as a multimodal probe with s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f89657a57677aa64cae530d96ac2ce2f
https://hdl.handle.net/10481/76963
https://hdl.handle.net/10481/76963
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
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
https://doi.org/10.15227/orgsyn.098.0374
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Universidad de Barcelona
We describe a novel transition metal-free method for the synthesis of N-difluoromethylated pyridines and 4-pyridones/quinolones by using readily available ethyl bromodifluoroacetate as a fluorine source. The formation of N-difluoromethylated pyridine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12922af5580bfbe2e85af8dae252c3ae
https://doi.org/10.1039/d0ra06322c
https://doi.org/10.1039/d0ra06322c
Autor:
Christina Tzitzoglaki, Anja Hoffmann, Andreea L. Turcu, Patrick Schmerer, Chunlong Ma, George Laros, Christos Liolios, Brea José, Jun Wang, Santiago Vázquez, Michaela Schmidtke, Antonios Kolocouris
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Universidad de Barcelona
Influenza A viruses can cause a serious future threat due to frequent mutations. Amantadine and rimantadine inhibit influenza A M2 wild-type (WT) viruses by binding and blocking M2 WT channel-mediated proton current. The resistant to the drugs amanta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6fef409d4be46202f5ff43f2c65748d
http://hdl.handle.net/2445/190102
http://hdl.handle.net/2445/190102
Autor:
Cabezas Giménez, Juanjo
Publikováno v:
TDX (Tesis Doctorals en Xarxa)
TDR. Tesis Doctorales en Red
instname
Repositori Institucional de la Universitat Rovira i Virgili
TDR. Tesis Doctorales en Red
instname
Repositori Institucional de la Universitat Rovira i Virgili
A través de la reacció d'un derivat d'aminoàcid i Cu(II) s'ha obtingut la xarxa metaloorgànica (MOF) quiral anomenada TAMOF-1. Per tal de ser utilitzada en la investigació de processos enantioselectius, la síntesi del TAMOF-1 s'ha optimitzat en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::99ca82e92ec0378eb37ee2a40b77df88
http://hdl.handle.net/10803/674267
http://hdl.handle.net/10803/674267
Autor:
Jamie I. Scott, Lorena Mendive-Tapia, Doireann Gordon, Nicole D. Barth, Emily J. Thompson, Zhiming Cheng, David Taggart, Takanori Kitamura, Alberto Bravo-Blas, Edward W. Roberts, Jordi Juarez-Jimenez, Julien Michel, Berber Piet, I. Jolanda de Vries, Martijn Verdoes, John Dawson, Neil O. Carragher, Richard A. O’ Connor, Ahsan R. Akram, Margaret Frame, Alan Serrels, Marc Vendrell
Publikováno v:
Nature Communications, 13, 1
Dipòsit Digital de la UB
Universidad de Barcelona
Scott, J, Mendive Tapia, L, Gordon, D, Barth, N, Thompson, E, Cheng, Z, Taggart, D, Kitamura, T, Blas, A B, Roberts, E W, Juarez Jimenez, J, Michel, J, Piet, B, de Vries, I J, Verdoes, M, Dawson, J C, Carragher, N O, O'Connor, R A, Akram, A R, Serrels, A, Frame, M C & Vendrell, M 2022, ' A fluorogenic probe for granzyme B enables in-biopsy evaluation and screening of response to anticancer immunotherapies ', Nature Communications . https://doi.org/10.1038/s41467-022-29691-w
Nature Communications, 13
Nature Communications
Dipòsit Digital de la UB
Universidad de Barcelona
Scott, J, Mendive Tapia, L, Gordon, D, Barth, N, Thompson, E, Cheng, Z, Taggart, D, Kitamura, T, Blas, A B, Roberts, E W, Juarez Jimenez, J, Michel, J, Piet, B, de Vries, I J, Verdoes, M, Dawson, J C, Carragher, N O, O'Connor, R A, Akram, A R, Serrels, A, Frame, M C & Vendrell, M 2022, ' A fluorogenic probe for granzyme B enables in-biopsy evaluation and screening of response to anticancer immunotherapies ', Nature Communications . https://doi.org/10.1038/s41467-022-29691-w
Nature Communications, 13
Nature Communications
Immunotherapy promotes the attack of cancer cells by the immune system; however, it is difficult to detect early responses before changes in tumor size occur. Here, we report the rational design of a fluorogenic peptide able to detect picomolar conce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::667b6fd358c7aa9be451c7f1650c50bd
https://doi.org/10.1038/s41467-022-29691-w
https://doi.org/10.1038/s41467-022-29691-w