Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Ana B, Cuenca"'
Autor:
Raúl Cosialls, Odile Fernández, Cristina Simó, Krishna R. Pulagam, Marta Guerra-Rebollo, Jordi Llop, Cristina Fornaguera, Ana B. Cuenca, Salvador Borrós
Publikováno v:
Journal of Controlled Release. 358:739-751
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4478a32213cb530a92aad1cbdce15c4f
https://doi.org/10.1016/j.jconrel.2023.05.017
https://doi.org/10.1016/j.jconrel.2023.05.017
Autor:
Victor Masip, Ángel Lirio, Albert Sánchez-López, Ana B. Cuenca, Raimon Puig de la Bellacasa, Pau Abrisqueta, Jordi Teixidó, José I. Borrell, Albert Gibert, Roger Estrada-Tejedor
Publikováno v:
Pharmaceuticals, Vol 14, Iss 12, p 1311 (2021)
Pyrido[2,3-d]pyrimidin-7(8H)-ones have attracted widespread interest due to their similarity with nitrogenous bases found in DNA and RNA and their potential applicability as tyrosine kinase inhibitors. Such structures, presenting up to five diversity
Externí odkaz:
https://doaj.org/article/97db14f395054d2a81849d0dda3b2cac
Autor:
Raúl, Cosialls, Cristina, Simó, Salvador, Borrós, Vanessa, Gómez-Vallejo, Claudia, Schmidt, Jordi, Llop, Ana B, Cuenca, Angela, Casini
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany).
To advance the design of self-assembled metallosupramolecular architectures as new generation theranostic agents, the synthesis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::656962978d5fa3cafbf71796df9f639b
https://pubmed.ncbi.nlm.nih.gov/36239701
https://pubmed.ncbi.nlm.nih.gov/36239701
Autor:
Ana B. Cuenca, Elena Fernández
Publikováno v:
Organic Reactions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf98c30c2e37fa3b4db96f3daa2a54b0
https://doi.org/10.1002/0471264180.or105.02
https://doi.org/10.1002/0471264180.or105.02
Autor:
Anton Cunillera, Alexandr Shafir, Ana B. Cuenca, Laura G Rodríguez, Marta Díaz Baranda, Wei W. Chen, Nahiane Pipaon Fernández
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Chemical Science
instname
Chemical Science
A stepwise build-up of multi-substituted Csp3 carbon centers is an attractive, conceptually simple, but often synthetically challenging type of disconnection. To this end, this report describes how gem-α,α-dimetalloid-substituted benzylic reagents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20c63aefbba49fd01f461dedf493d487
https://doi.org/10.1039/d1sc01741a
https://doi.org/10.1039/d1sc01741a
Autor:
Wei W. Chen, Anton Cunillera, Dandan Chen, Sébastien Lethu, Albert López de Moragas, Jun Zhu, Miquel Solà, Ana B. Cuenca, Alexandr Shafir
Publikováno v:
Angewandte Chemie. 132:20376-20382
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::786722b465e47568df2256ff81f79202
https://doi.org/10.1002/ange.202009369
https://doi.org/10.1002/ange.202009369
Publikováno v:
Angewandte Chemie International Edition. 59:16294-16309
Hypervalent organoiodane reagents are ubiquitous in organic synthesis, both as oxidants and as electrophilic group-transfer agents. In addition to these hallmark applications, a complementary strategy is gaining momentum that exploits the ability of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::432594e309649fcec63945f3562e2863
https://doi.org/10.1002/anie.201908418
https://doi.org/10.1002/anie.201908418
Autor:
Elena Fernández, Ana B. Cuenca
Publikováno v:
Chemical Society reviews. 50(1)
The condensation of easy manageable lithium α-bis(boryl)carbanions with carbonyl derivatives, the so-called boron-Wittig reaction, allows for the straightforward and often stereoselective formation of synthetically highly versatile metalloid-substit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b7e0b072f9415aa25c7ad1bc4e86343
https://pubmed.ncbi.nlm.nih.gov/33319887
https://pubmed.ncbi.nlm.nih.gov/33319887
Publikováno v:
European Journal of Organic Chemistry. 2018:2728-2739
Gem-diborylalkenes have emerged as efficient reagents for selective cross-coupling reactions, reduction approaches and Michael additions. The synthesis of 1,1-diborylalkenes involves condensation of polyborated compounds with aldehydes or ketones fol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::623cc214e8c3c5dc2113b038b802b704
https://doi.org/10.1002/ejoc.201701786
https://doi.org/10.1002/ejoc.201701786