Publications
Jan 2023 Sou um título. Clique e edite.
Jan 2023 Sou um título. Clique e edite.
Jan 2023 Sou um título. Clique e edite.
Jan 2023 Sou um título. Clique e edite.
80
Org. Chem. Front. 2022, accepted
Rongalite in PEG-400 as a general and reusable system for the synthesis of 2,5-disubstituted chalcogenophenes
D. B. Paixão, E. G. O. Soares, H. D. Salles, C. D. G. Silva, D. S. Rampon and P. H. Schneider
79
Química Orgânica Sintética
Brasil 2022
Compostos Orgânicos Funcionalizados com Calcogênio: Síntese Assimétrica e Materiais Orgânicos Funcionais
P. H. Schneider
78
Org. Biomol. chem, 2022, 20, 6072-6177
Transition metal catalysed direct sulfanylation of unreactive C-H bonds: an overview of the last two decades
D. Rampon, D. Seckler, E. Q. da Luz, D. B. Paixão, A. M. E. Larroza, P. H. Schneider, D. Alves
77
Elsevier's Series of "Advances in Green and Sustainable Chemistry"
Advances in photochemical seleno-functionalization of (hetero)arenes
J. Rafique, J. B. Azeredo, S. Saba, P. H, Schneider, A. L. Braga
76
Chem. Biodiv., 2022, 19, e202100793
One-pot synthesis and in silico molecular docking studies of arylselanyl hydrazides as potential antituberculosis agents
E. L. Borges, H. A. Goulart, G. Perin, P. H. Schneider, G. S. Rieder, P. A. Nogara, J. B. T. Rocha
75
J. Org. Chem., 2021, 86, 10140-10153
Evidence of a Photoinduced Electron-Transfer Mechanism in the Fluorescence Self-quenching of 2,5-Substituted Selenophenes Prepared through In Situ Reduction of Elemental Selenium in Superbasic Media
H. D. de Salles, D. B. Paixão, C. A. Barboza, D. S. Rampon, F. L. Coelho, F. S. Rodembusch, P. H. Schneider
74
Chem. Rec., 2021, 21, 2739-2761
Light‐mediated Seleno‐Functionalization of Organic Molecules: Recent Advances
J. Rafique, D. S. Rampon, J. B. Azeredo, F. L. Coelho, P. H. Schneider, A. L. Braga
73
Trithiocarbonate anion as a sulfur source for the synthesis of 2,5-disubstituted thiophenes and 2-substituted benzo[b]thiophenes
D. B. Paixão, D. S. Rampon, H. D. Salles, E. G. O. Soares, F. N. Bilheri, P. H. Schneider
72
J. Org. Chem., 2020, 85, 12922–12934
Trithiocarbonate anion as a sulfur source for the synthesis of 2,5-disubstituted thiophenes and 2-substituted benzo[b]thiophenes
D. B. Paixão, D. S. Rampon, H. D. Salles, E. G. O. Soares, F. N. Bilheri, P. H. Schneider
71
Ultrason. Sonochem., 2020, 68, 105228
Ultrasound-promoted regioselective synthesis of chalcogeno-indolizines by a stepwise 1,3-dipolar cycloaddition
M. M. Vieira, B. T. Dalberto, F. L. Coelho, P. H. Schneider
70
J. Mol. Liq., 2020, 313, 113525
Non-traditional intrinsic luminescence of amphiphilic-based ionic liquids from oxazolidines: Interaction studies in phosphatidylcholine-composed liposomes and BSA optical sensing in solution
L. C. Borba, C. H. Griebeler, M. F. Bach, C. A. Barbosa, P. A. Nogara, J. B. T. Rocha, S. S. Amaral, F. S. Rodembusch, P. H. Schneider
69
RSC Adv., 2020, 10, 10502-10509
Photoinduced metal-free a-selenylation of ketones
B. T. Dalberto, P. H. Schneider
68
J. Mol Struct., 2020, 1207, 127817
Ground and excited-state properties of 1,3-benzoselenazole derivatives: A combined theoretical and experimental photophysical investigation
C. S. Radatz, F. L. Coelho, E. S. Gil, F. S. Santos, J. M. F. M. M. Schneider, P. F. B. Gonçalves, F. S. Rodembusch, P. H. Schneider
67
Appl. Cat. A-Gen., 2020, 594, 117444
Strategy to isolate ionic gold sites on silica surface: Increasing their efficiency as catalyst for the formation of 1,3-diynes
C. A. Didó, F. L. Coelho, M. B. Closs, M. Deon, F. Horowitz, F. Bernardi, P. H. Schneider, E. V. Benvenutti
66
Arab. J. Chem, 2020, 13, 883-889
Synthesis of enantiomerically pure glycerol derivatives containing an organochalcogen unit: In vitro and in vivo antioxidant activity
P. C. Nobre, H. A. Vargas, C. G. Jacoby, P. H. Schneider, A. M Casaril, L. Savegnago, R. F. Schumacher, E. J. Lenardão, D. S. Ávila, L. B. L. Rodrigues Junior, G. Perin
65
Tetrahedron, 2020, 76, 130874
Asymmetric Michael Reaction Promoted by Chiral Thiazolidine-Thiourea Catalyst
T. L. da Silva, R. S. Rambo, C. G. Jacoby, P. H. Schneider
64
Appl. Clay Sci., 2019, 182, 105291
Clay-based Janus nanoparticles as compatibilizing agent in polymer blends
T. S. Daitx, C. G. Jacoby, C. I. Ferreira, P. H. Schneider, R. S. Mauler,
63
INPI BR 10 2019 017050 6
Processo para a Obtenção de Polímeros Contendo Selênio com Propriedades de Autocura
T. S. Daitx, C. G. Jacoby, R. S. Mauler, P. H. Schneider
62
Dalton Trans., 2019, 48, 9851-9905
Transition Metal Catalysed Direct Selanylation of Arenes and Heteroarenes
D. S. Rampon, E. Q. Luz, D. B. Lima, R. A. Balaguez, P. H. Schneider, D. Alves
61
Chem. -Eur. J., 2019, 25, 8157-8162
Intramolecular hydroamination of selenoalkynes to 2-selenylindole in absence of catalyst
F. L. Coelho, E. S. Gil, P. F. B. Gonçalves, L. F. Campo, P. H. Schneider
60
New J. Chem., 2019, 43, 11596-11603
Straightforward Synthesis of Photoactive Chalcogen Functionalized Benzimidazo[1,2-a]quinolines
R. B. da Silva, F. L. Coelho, F. S. Rodembusch, R. S. Schwab, J. M. F. M. Schneider, D. S. Rampon, P. H. Schneider
59
J. Braz. Chem. Soc., 2019, 30, 1825-1833
Imidazo[1,2-a]pyridine A3-coupling catalyzed by a Cu/SiO2 material
H. D. De Salles, T. L. da Silva, C. Radatz, R. F. Affeldt, E. V. Benvenutti, P. H. Schneider
58
Catal. Commun. 2019, 121, 19-26
New arylselanylpirazole-copper catalysis: Highly efficient catalytic system for CSe e CS coupling reactions
F. L. Coelho, L. C. Dresch, R. Stieler, L. F. Campo, P. H. Schneider
57
New J. Chem., 2018, 42, 7416-7421
Highly efficient organocatalysts for the asymmetric aldol reaction
C. G. Jacoby, P. H. V. Vontobel, M. F. Bach, P. H. Schneider
56
Eur. J. Org. Chem., 2018, 6738-6742
Visible-light promoted stereoselective arylselanyl functionalization of alkynes
A. C. H. Weber, F. L. Coelho, R. F. Affeldt, P. H. Schneider
55
RSC Adv., 2017, 7, 8832-8842
Dipolar vinyl sulfur fluorescent dyes. Synthesis and photophysics of sulfide, sulfoxide and sulfone based D-π-A compounds
M. Monçalves, G. M. Zanotto, J. M. Toldo, D. S. Rampon, P. H. Schneider, P. F. B. Gonçalves, F. S. Rodembusch, C. C. Silveira
54
Neurosci. Lett. 2017, 651, 182-187
Evaluation of Se-phenyl-thiazolidine-4-carboselenoate protective activity against oxidative and behavioral stress in the maniac model induced by ouabain in male rats
F. S. S. Sousa, N. Seus, D. Alves, H. D. Salles, P. H. Schneider, L. Savegnago, M. Castro
53
Mol. Catal. 2017, 427, 73-79
Silver-catalyzed direct selenylation of terminal alkynes trough C-H bond functionalization
M. C. D. F. Xavier, B. Goldani, R. F. Schumacher, G. Perin, P. H. Schneider, D. Alves
52
Eur. J. Org. Chem, 2017,46, 6997-7004
Design of a chiral ionic liquid system for the enantioselective addition of diethylzinc to aldehydes
M. F. Bach, C. H. Griebeler, C. G. Jacoby, P. H. Schneider
51
New J. Chem., 2016, 40, 2321-2326
Synthesis of enantiomerically pure bis (2,2-dimethyl-1,3-dioxolanylmethyl)chalcogenides and dichalcogenides
E. L. Borges, T. J. Peglow, M. S. Silva, C. G. Jacoby, P. H. Schneider, E. J. Lenardão, R. G. Jacob, G. Perin
50
J. Chromatogr. B, 2016, 1020, 43-52
A bioanalytical HPLC method for coumestrol quantification in skin permeation tests followed by UPLC-QTOF/HDMS stability-indicating method for identification of degradation products
S. E. Bianchi, H. F. Teixeira, S. Kaiser, G. G. Ortega, P. H. Schneider, V. L. Bassani
49
RSC Adv., 2016, 6, 49613-49624
Bis-arylsulfenyl- and bis-arylselanyl-benzo-2,1,3-thiadiazoles: synthesis and photophysical characterization
R. A. Balaguez, V. G. Ricordi, R. C. Duarte, J. M. Toldo, C. M. Santos, P. H. Schneider, P. F. B. Gonçalves, F. S. Rodembusch, D. Alves
48
Tetrahedron Lett., 2016, 57, 3501-3504
Straightforward synthesis and antioxidant studies of chalcogenoaziridines
R. Borges, F. C. D. Floyd, R. S. Schwab, F. S. S. Sousa, M. N. de Souza, L. Savegnago, P. H. Schneider
47
Curr. Pharm. Biotec., 2015, 16, 66-71
Isolation of Achyrobichalcone from Achyrocline satureioides by High- Speed Countercurrent Chromatography
J. Carini, G. Leitão, P. H. Schneider, C. Santos, F. Costa, M. Holzschuh, F. Klamt, V. Bassani
46
J. Mol. Cat. A., 2015, 399, 71-78
Covalently Immobilized Indium (III) Composite (In/SiO2) as Highly Efficient Reusable Catalyst for A3-Coupling of Aldehydes, Alkynes and Amines under Solvent-Free Conditions
T. L. da Silva, R. S. Rambo, D. S. Rampon, C. S. Radatz, E. V. Benvenutti, D. Russowsky, P. H. Schneider
45
Tetrahedron Lett. 2015, 21, 2735-2740
Synthesis of Benzoselenazoles and Benzoselenazolines by Cyclization of 2-Amino Selenophenol with β-Dicarbonyl Compounds
R. A. Balaguez, R. K. Krüger, C. S. Radatz, D. S. Rampon, E. J. Lenardão, P. H. Schneider, D. Alves
44
Tetrahedron: Asymmetry 2015, 26, 632-637
A highly enantio- and diastereoselective direct aldol reaction in aqueous medium catalyzed by thiazolidine-based compounds
R. S. Rambo, C. G. Jacoby, T. L. da Silva, P. H. Schneider
43
Tetrahedron Lett 2015, 48, 6674-6680
New thioureas based on thiazolidines with antioxidant potential
T. L. da Silva, L. M. F. Miolo, F. S. S. Sousa, L. M. P. Brod. L. Savegnago, P. H. Schneider
42
Dyes Pigments 2014, 102, 71-78
Divinyl sulfides/sulfones-based D–π–A–π–D dyes as efficient non-aromatic bridges for π-conjugated compounds
M. Monçalves, D. S. Rampon, P. H. Schneider, F. S. Rodembusch, C. C. Silveira
41
New J. Chem. 2014, 38, 1410-1417
Recoverable Cu/SiO2 composite-catalysed click synthesis of 1,2,3-triazoles in water media
C. S. Radatz, L. A. Soares, E. R. Vieira, D. Alves, D. Russowsky, P. H. Schneider
40
J. Braz. Chem. Soc. 2014, 25, 1493-1503
Synthesis of New Family of Thiazoline and Thiazole Esters and Investigation of their Thermal Properties
J. M. F. M. Schneider, E. S. Sales, A. A. Merlo, P. R. Livotto, P. H. Schneider
39
J. Org. Chem. 2014, 79, 5987-5992
Palladium-Catalyzed Direct Arylation of Selenophene
D. S. Rampon, L. A. Wessjohann, P. H. Schneider
38
Prog. Neuro-Psychoph. 2014, 54, 187-194
Anxiolytic effects of diphenyl diselenide on adult zebrafish in a novelty paradigm
M. Ibrahim, B. M. Mussulini, L. Moro, A. M. de Assis, D. B. Rosemberg, D. L. de Onofre, J. B. T. Rocha, R. S. Schwab, P. H. Schneider, D. O. Souza, E. Rico
37
Eur. J. Org. Chem. 2014, 6945-6952
Synthesis of 2‐Substituted 1,3‐Benzoselenazoles from Carboxylic Acids Promoted by Tributylphosphine
C. S. Radatz, D. S. Rampon, R. A. Balaguez, D. Alves, P. H. Schneider
36
Chem-Biol. Interact. 2013, 25, 100-107
Antioxidant properties of (R)-Se-aryl thiazolidine-4-carboselenoate
F. N. Victoria, D. M. Martinez, M. Castro, A. M. Casaril, D. Alves, E. J. Lenardão, H. D. de Salles, P. H. Schneider, L. Savegnago
35
Quim. Nova, 2013, 36, 1591-1599
Catálise Assimétrica no Brasil: Desenvolvimento e Potencialidades para o Avanço da Indústria Química Brasileira
A. L. Braga, D. S. Ludtke, P. H. Schneider, M. W. Paixão, L. H. de Andrade
34
J. Phys. Org. Chem. 2013, 27, 336-343
Ground and excited state properties of chalcogenol esters: a combined theoretical and experimental study
D. S. Rampon, F. S. Santos, R. R. Descalzo, J. M. Toldo, P. F. B. Gonçalves, P. H. Schneider, F. S. Rodembusch
33
Tetrahedron 2013, 69, 1316-1321
Direct synthesis of 2-aryl-1,3-benzoselenazoles by reaction of bis(2-aminophenyl) diselenides with aryl aldehydes using sodium metabisulfite
C. S. Radatz, D. S. Alves , P. H. Schneider
32
Liq. Cryst. 2012, 39, 175-784
The 2:1 cycloadducts from [3 + 2] 1,3-dipolar cycloaddition of nitrile oxide and vinylacetic acid. Synthesis and liquid crystal behaviour
A. T. Tavares, G. D. Vilela, J. Toldo, P. F. B. Gonçalves, J. Eccher, I. H. Bechtold, R. C. Viscovini, P. H. Schneider, A. A. Merlo
31
Liq. Cryst. 2012, 39, 769-777
Selenides and diselenides containing oxadiazoles: a new class of functionalised materials
T. E. Frizon, D. S. Rampon, H. Gallardo,. A. A. Merlo, P. H. Schneider, O. E. D. Rodrigues, A. L. Braga
30
Brain Res. 2012, 1475, 31-36
Effects of Se-phenyl thiazolidine-4-carboselenoate on mechanical and thermal hyperalgesia in brachial plexus avulsion in mice: Mediation by cannabinoid CB1 and CB2 receptors
C. R. Jesse, L. del Fabbro, C. Filho, L. Souza, L. Savegnago, D. Alves, P. H. Schneider, H. D. de Salles
29
Tetrahedron 2012, 68, 10449-10455
Straightforward synthesis of non-natural chalcogen peptides via ring opening of aziridines
R. S. Schwab, P. H. Schneider