Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Talita de A. Fernandes"'
Autor:
Brenno A. D. Neto, José R. Corrêa, Juliano A. Chaker, Paulo Eduardo Narcizo de Souza, Daniel F. S. Machado, Elaine R Sodre, Valter H. Carvalho-Silva, Claudia C. Gatto, Talita de A. Fernandes, Bruna C. Guido
Publikováno v:
The Journal of Organic Chemistry. 85:12614-12634
An aggregation-induced emission enhancement (AIEE) effect in fluorescent lipophilic 2,1,3-benzothiadiazole (BTD) derivatives and their organic nanoaggregates were studied. A set of techniques such as single-crystal X-ray, dynamic light scattering (DL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e36353b8f53291af3f485412404eeed
https://doi.org/10.1021/acs.joc.0c01805
https://doi.org/10.1021/acs.joc.0c01805
Autor:
Talita de A. Fernandes, Jorge L.O. Domingos, Carmen Nájera, Paulo R. R. Costa, José M. Sansano, Luana G. de Souza, Magdalena N. Rennó
Publikováno v:
RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
Universidad de Alicante (UA)
The enantioselective electrophilic fluorination of α-aryl-tetralones is promoted by cinchonine/selectfluor combinations. This strategy allows a facile synthesis of the corresponding 2-fluoro-2-aryl-1-tetralones with excellent yields (up to >98%) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::549970d2c3e1c986015fe0ec98993760
https://doi.org/10.1016/j.jfluchem.2018.11.007
https://doi.org/10.1016/j.jfluchem.2018.11.007
Autor:
Talita de A. Fernandes, F. Dean Toste, Matthew S. Sigman, Jeffrey Mckenna, Richard T. Thornbury, Celine B. Santiago, Eric P. A. Talbot, Vaneet Saini
Publikováno v:
Chemical Science. 8:2890-2897
A mild palladium-catalyzed ligand-controlled regioselective 1,3-arylfluorination of 2[H]-chromenes has been developed. The products with a syn-1,3 substitution pattern were obtained with high enantiomeric excess using a PyrOx ligand, wherein the util
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9d6314c9c7ca2a45a348d58a18aab80
https://doi.org/10.1039/c6sc05102b
https://doi.org/10.1039/c6sc05102b
Autor:
Edézio Ferreira Cunha-Júnior, Talita de A. Fernandes, Georgia C. Atella, Paulo R. R. Costa, Valter Viana Andrade-Neto, Marilene M. Canto-Cavalheiro, Eduardo Caio Torres-Santos
Publikováno v:
Antimicrobial Agents and Chemotherapy. 60:6844-6852
Leishmaniasis affects mainly low-income populations in tropical regions. Radical innovation in drug discovery is time-consuming and expensive, imposing severe restrictions on the ability to launch new chemical entities for the treatment of neglected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1105aafaca302e3dd2f992ba8e57a539
https://doi.org/10.1128/aac.01545-16
https://doi.org/10.1128/aac.01545-16
Autor:
Paulo R. R. Costa, Talita de A. Fernandes, Dinesh Manvar, Amartya Basu, Jorge L.O. Domingos, Daniel Brian Nichols, Neerja Kaushik-Basu
Publikováno v:
European Journal of Medicinal Chemistry. 112:33-38
The synthesis of a series of 5-carba-pterocarpens derivatives involving the cyclization of α-aryl-α-tetralones is described. Several compounds demonstrated potent activity and selectivity in vitro against HCV replicon reporter cells. The best profi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f4cb7cce8be185377f5972956ba7513
https://doi.org/10.1016/j.ejmech.2016.02.010
https://doi.org/10.1016/j.ejmech.2016.02.010
Autor:
Dinesh Manvar, Talita de A. Fernandes, Paulo R. R. Costa, Amartya Basu, Jorge L.O. Domingos, Erdenechimeg Baljinnyam, Eurides F.T. Junior, Neerja Kaushik-Basu
Publikováno v:
European Journal of Medicinal Chemistry. 93:51-54
The synthesis of a novel series of 1-carba-isoflavanones through the α-arylation of α-tetralones is described. Several of these compounds demonstrated potent activity and selectivity in-vitro against HCV replicon reporter cells. Compound 10 (LQB-31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3157b3348f76afd73ef566dabfe6e8f
https://doi.org/10.1016/j.ejmech.2015.01.057
https://doi.org/10.1016/j.ejmech.2015.01.057
Autor:
Paulo R. R. Costa, Jorge L. O. Domingos, Sabrina de Medeiros, Talita de A. Fernandes, Luiza I. A. da Rocha, Carmen Nájera
Publikováno v:
European Journal of Organic Chemistry. 2014:1314-1320
Financial support from the Brazilian agencies Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES-DGU Project number 200/09), Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq), Fundacao de Amparo a Pesquisa do Estado
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93dc84cfe3c7fa9c83e129fc178e77bc
https://doi.org/10.1002/ejoc.201301505
https://doi.org/10.1002/ejoc.201301505
Autor:
Talita de A. Fernandes, João M. J. M. Ravasco, Carmen Nájera, José M. Sansano, Béla Fiser, Paulo R. R. Costa, Pascuala Vizcaino‐Milla, Enrique Gómez-Bengoa, Aitor Ortega-Martínez
Publikováno v:
ChemInform. 47
The title catalyst is applied in the Michael reaction of α,α-branched aldehydes to nitroalkenes (I) and maleimides (IV).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::061479f6550bd0ba23abac7b4d550fd7
https://doi.org/10.1002/chin.201623031
https://doi.org/10.1002/chin.201623031
Autor:
José M. Sansano, Aitor Ortega-Martínez, Pascuala Vizcaino‐Milla, Paulo R. R. Costa, Enrique Gómez-Bengoa, João M. J. M. Ravasco, Béla Fiser, Talita de A. Fernandes, Carmen Nájera
Publikováno v:
RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
Universidad de Alicante (UA)
Bifunctional chiral primary amine 8 containing an (S,S)-trans-cyclohexane-1,2-diamine scaffold and a 2-benzimidazole unit is used as a general organocatalyst for the Michael addition of α,α-branched aldehydes to nitroalkenes and maleimides. The rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ba0fa7e152a8c743ba50c0019eb0e2d
http://hdl.handle.net/10045/52712
http://hdl.handle.net/10045/52712
