Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Isadora, Tisoco"'
Autor:
Inaiá O. Rocha, Yuri G. Kappenberg, Wilian C. Rosa, Clarissa P. Frizzo, Nilo Zanatta, Marcos A. P. Martins, Isadora Tisoco, Bernardo A. Iglesias, Helio G. Bonacorso
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 2799-2811 (2021)
A new series of ten examples of Schiff bases, namely (E)-2-(((2-alkyl(aryl/heteroaryl)-4-(trifluoromethyl)quinolin-6-yl)imino)methyl)phenols 3, was easily synthesized with yields of up to 91% from the reactions involving a series of 2-(R-substituted)
Externí odkaz:
https://doaj.org/article/ca2f6fa7a5d642028b322cc744260341
Autor:
Isadora Tisoco, Maria Carolina Donatoni, Henrique Fernandes Vieira Victória, José Roberto de Toledo, Klaus Krambrock, Otávio Augusto Chaves, Kleber Thiago de Oliveira, Bernardo Almeida Iglesias
Publikováno v:
Dalton Transactions. 51:1646-1657
Novel Pt(ii)- and Pd(ii) cationic porphyrins in photobiological process applications.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d641cdf011ff55fffab0b9887dd76022
https://doi.org/10.1039/d1dt03565g
https://doi.org/10.1039/d1dt03565g
Autor:
Helio Gauze Bonacorso, Gabriel Costa Santos, Yuri G. Kappenberg, Jessica M.L. Rosa, Alex Ketzer, Isadora Tisoco, Marcos A. P. Martins, Nilo Zanatta, Clarissa P. Frizzo, Bernardo A. Iglesias
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d31da8854680ce78ec863ed5d9c9a2f
https://doi.org/10.2139/ssrn.4395688
https://doi.org/10.2139/ssrn.4395688
Autor:
Bianca Dozza, Bruna M. Rodrigues, Isadora Tisoco, Vitória B. de Souza, Lúcio Angnes, Bernardo A. Iglesias
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fce0ff7a86164113e2d822dceae9015
https://doi.org/10.1016/j.microc.2022.108041
https://doi.org/10.1016/j.microc.2022.108041
Autor:
Isadora Tisoco, Bernardo A. Iglesias, Diego Alves, Allya Larroza, Lucielli Savegnago, Joel S. Reis, Mariana G. Fronza, Davi F. Back, Roberta Krüger
Publikováno v:
The Journal of organic chemistry. 86(24)
A range of bis-triazolylchalcogenium-BTD 3 was synthesized by a copper-catalyzed azide-alkyne cycloaddition of azido arylchalcogenides 1 and 4,7-diethynylbenzo[c][1,2,5]thiadiazole 2. Eight new compounds were obtained in moderate to good yields using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06cabfd398d0d9e5eac9065e2207bcca
https://pubmed.ncbi.nlm.nih.gov/34843245
https://pubmed.ncbi.nlm.nih.gov/34843245
Autor:
Inaiá O Rocha, Yuri G Kappenberg, Wilian C Rosa, Clarissa P Frizzo, Nilo Zanatta, Marcos A P Martins, Isadora Tisoco, Bernardo A Iglesias, Helio G Bonacorso
A new series of ten examples of (E)-2-(((2-alkyl(aryl/heteroaryl)-4-(trifluoromethyl)quinolin-6-yl)imino)methyl)phenols (Schiff bases), was easy synthesized at yields up to 91% from the reactions involving a series of 2-(R-substituted) 6-amino-4-(tri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2105a1c5893a0e28ae42c709b5484ea
https://doi.org/10.3762/bxiv.2021.60.v1
https://doi.org/10.3762/bxiv.2021.60.v1
Autor:
Nilo Zanatta, Helio G. Bonacorso, Wilian C. Rosa, Yuri G. Kappenberg, Isadora Tisoco, Marcos A. P. Martins, Bernardo A. Iglesias, Clarissa P. Frizzo, Inaiá O. Rocha
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 2799-2811 (2021)
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 2799-2811 (2021)
A new series of ten examples of Schiff bases, namely (E)-2-(((2-alkyl(aryl/heteroaryl)-4-(trifluoromethyl)quinolin-6-yl)imino)methyl)phenols 3, was easily synthesized with yields of up to 91% from the reactions involving a series of 2-(R-substituted)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58f58bbbaabf7a04d45db93b2e1eea63
https://pubmed.ncbi.nlm.nih.gov/34925619
https://pubmed.ncbi.nlm.nih.gov/34925619
Autor:
Marcos A. P. Martins, Bernardo A. Iglesias, Clarissa P. Frizzo, Inaiá O. Rocha, Helio G. Bonacorso, Isadora Tisoco, Wilian C. Rosa, Nilo Zanatta, Yuri G. Kappenberg
Publikováno v:
SSRN Electronic Journal.
A new series of ten examples of (E)-2-(((2-alkyl(aryl/heteroaryl)-4-(trifluoromethyl)quinolin-6-yl)imino)methyl)phenols (Schiff bases), was easy synthesized at yields of up to 91% from the reactions between a series of 2-(R-substituted) 6-amino-4-(tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91a2d970b720cfa6ae238ad836f427fe
https://doi.org/10.2139/ssrn.3861476
https://doi.org/10.2139/ssrn.3861476
Autor:
Gabriel C, Santos, Inaiá O, Rocha, Felipe S, Stefanello, João P P, Copetti, Isadora, Tisoco, Marcos A P, Martins, Nilo, Zanatta, Clarissa P, Frizzo, Bernardo A, Iglesias, Helio G, Bonacorso
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 269:120768
This paper describes the synthesis, structural study, and evaluation of electrochemical and photophysical properties by UV-Vis absorption and fluorescence emission analysis (solution and solid-state) of a series of eight 3,5-aryl-substituted 1-phenyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68d71300f7731bc271a1e54b63ab8ca4
https://doi.org/10.1016/j.saa.2021.120768
https://doi.org/10.1016/j.saa.2021.120768
Autor:
Wilian C. Rosa, Helio G. Bonacorso, Nilo Zanatta, Isadora Tisoco, Bruna F. Schmitz, Marcos A. P. Martins, Inaiá O. Rocha, Bernardo A. Iglesias
Publikováno v:
Journal of Fluorine Chemistry. 248:109822
A series of seven novel scaffolds of 2-substituted 4-trifluoromehyl-5H-chromeno[4,3-b]pyridin-5-ones (3a-g), where R (2-substituents) = Me, Ph, 4-tolyl, 4-NO2C6H4, 4-FC6H4, 4-BrC6H4, and 2-thienyl, were easily and regioselectively synthesized by empl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d3ba1eef6c37851548a955f322736f4
https://doi.org/10.1016/j.jfluchem.2021.109822
https://doi.org/10.1016/j.jfluchem.2021.109822