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Artigo de periodico
The interaction of Hg2+ and trivalent ions with two new fluorescein bio-inspired dual colorimetric/fluorimetric probes (2016)
Gonçalves, A. C; Pila, V; Oliveira, E; Santos, S. M; J. L. Capelo; Santos, Alcindo Aparecido dos ; Lodeiro, C
Source: Dalton Transactions. Unidade: IQ
Subjects: COLORIMETRIA, LUMINESCÊNCIA
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GONÇALVES, A. C et al. The interaction of Hg2+ and trivalent ions with two new fluorescein bio-inspired dual colorimetric/fluorimetric probes. Dalton Transactions, v. 45, n. 23, p. 9513-9522 : + supplementary materials (S1-S13), 2016Tradução . . Disponível em: https://doi.org/10.1039/c6dt01180b. Acesso em: 07 jul. 2024.
APA
Gonçalves, A. C., Pila, V., Oliveira, E., Santos, S. M., J. L. Capelo,, Santos, A. A. dos, & Lodeiro, C. (2016). The interaction of Hg2+ and trivalent ions with two new fluorescein bio-inspired dual colorimetric/fluorimetric probes. Dalton Transactions, 45( 23), 9513-9522 : + supplementary materials (S1-S13). doi:10.1039/c6dt01180b
NLM
Gonçalves AC, Pila V, Oliveira E, Santos SM, J. L. Capelo, Santos AA dos, Lodeiro C. The interaction of Hg2+ and trivalent ions with two new fluorescein bio-inspired dual colorimetric/fluorimetric probes [Internet]. Dalton Transactions. 2016 ; 45( 23): 9513-9522 : + supplementary materials (S1-S13).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c6dt01180b
Vancouver
Gonçalves AC, Pila V, Oliveira E, Santos SM, J. L. Capelo, Santos AA dos, Lodeiro C. The interaction of Hg2+ and trivalent ions with two new fluorescein bio-inspired dual colorimetric/fluorimetric probes [Internet]. Dalton Transactions. 2016 ; 45( 23): 9513-9522 : + supplementary materials (S1-S13).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c6dt01180b
Artigo de periodico
On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds (2016)
Avila, Thais C; Reginato, Marcelo M; Di Vitta, Cláudio ; Ducati, Lucas Colucci ; Andrade, Leandro Helgueira ; Marzorati, Liliana
Source: Tetrahedrom Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, COMPOSTOS ORGÂNICOS
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AVILA, Thais C et al. On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds. Tetrahedrom Letters, v. 57, p. 2152-2157, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.03.109. Acesso em: 07 jul. 2024.
APA
Avila, T. C., Reginato, M. M., Di Vitta, C., Ducati, L. C., Andrade, L. H., & Marzorati, L. (2016). On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds. Tetrahedrom Letters, 57, 2152-2157. doi:10.1016/j.tetlet.2016.03.109
NLM
Avila TC, Reginato MM, Di Vitta C, Ducati LC, Andrade LH, Marzorati L. On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds [Internet]. Tetrahedrom Letters. 2016 ; 57 2152-2157.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2016.03.109
Vancouver
Avila TC, Reginato MM, Di Vitta C, Ducati LC, Andrade LH, Marzorati L. On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds [Internet]. Tetrahedrom Letters. 2016 ; 57 2152-2157.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2016.03.109
Artigo de periodico
Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures (2015)
Santin, Luiza R. R; Santos, Sandra Carvalho dos; Novo, Diogo La Rosa; Bianchini, Daniela; Gerola, Adriana P; Braga, Gustavo; Caetano, Wilker; Moreira, Leonardo M; Bastos, Erick Leite ; Romani, Ana Paula; Oliveira, Hueder P. M. de
Source: Dyes and Pigments. Unidade: IQ
Subjects: FLUORESCÊNCIA, SOLVENTE
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SANTIN, Luiza R. R et al. Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures. Dyes and Pigments, v. 119, p. 12-21, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2015.03.004. Acesso em: 07 jul. 2024.
APA
Santin, L. R. R., Santos, S. C. dos, Novo, D. L. R., Bianchini, D., Gerola, A. P., Braga, G., et al. (2015). Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures. Dyes and Pigments, 119, 12-21. doi:10.1016/j.dyepig.2015.03.004
NLM
Santin LRR, Santos SC dos, Novo DLR, Bianchini D, Gerola AP, Braga G, Caetano W, Moreira LM, Bastos EL, Romani AP, Oliveira HPM de. Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures [Internet]. Dyes and Pigments. 2015 ; 119 12-21.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2015.03.004
Vancouver
Santin LRR, Santos SC dos, Novo DLR, Bianchini D, Gerola AP, Braga G, Caetano W, Moreira LM, Bastos EL, Romani AP, Oliveira HPM de. Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures [Internet]. Dyes and Pigments. 2015 ; 119 12-21.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2015.03.004
Artigo de periodico
Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems (2015)
khalid, Muhammad; Souza Junior, Sergio Pereira de; Ciscato, Luiz Francisco Monteiro Leite; Bartoloni, Fernando Heering; Baader, Wilhelm Josef
Source: Photochemical & Photobiological Sciences. Unidade: IQ
Subjects: BIOLUMINESCÊNCIA, QUÍMICA ORGÂNICA
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KHALID, Muhammad et al. Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems. Photochemical & Photobiological Sciences, v. 14, n. 7, p. 1296-1305, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5pp00152h. Acesso em: 07 jul. 2024.
APA
khalid, M., Souza Junior, S. P. de, Ciscato, L. F. M. L., Bartoloni, F. H., & Baader, W. J. (2015). Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems. Photochemical & Photobiological Sciences, 14( 7), 1296-1305. doi:10.1039/c5pp00152h
NLM
khalid M, Souza Junior SP de, Ciscato LFML, Bartoloni FH, Baader WJ. Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems [Internet]. Photochemical & Photobiological Sciences. 2015 ; 14( 7): 1296-1305.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5pp00152h
Vancouver
khalid M, Souza Junior SP de, Ciscato LFML, Bartoloni FH, Baader WJ. Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems [Internet]. Photochemical & Photobiological Sciences. 2015 ; 14( 7): 1296-1305.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5pp00152h
Parte de monografia/livro
Thallium-based catalysts (2015)
Carneiro, Vânia Maria Teixeira; Longo Junior, Luiz Sidney; Silva Junior, Luiz Fernando da
Source: Sustainable Catalysis: With Non-endangered Metals, Part 2. Unidade: IQ
Subjects: TÁLIO, QUÍMICA INORGÂNICA, CATALISADORES
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CARNEIRO, Vânia Maria Teixeira e LONGO JUNIOR, Luiz Sidney e SILVA JUNIOR, Luiz Fernando da. Thallium-based catalysts. Sustainable Catalysis: With Non-endangered Metals, Part 2. Tradução . Cambridge: Royal Society of Chemistry, 2015. . . Acesso em: 07 jul. 2024.
APA
Carneiro, V. M. T., Longo Junior, L. S., & Silva Junior, L. F. da. (2015). Thallium-based catalysts. In Sustainable Catalysis: With Non-endangered Metals, Part 2. Cambridge: Royal Society of Chemistry.
NLM
Carneiro VMT, Longo Junior LS, Silva Junior LF da. Thallium-based catalysts. In: Sustainable Catalysis: With Non-endangered Metals, Part 2. Cambridge: Royal Society of Chemistry; 2015. [citado 2024 jul. 07 ]
Vancouver
Carneiro VMT, Longo Junior LS, Silva Junior LF da. Thallium-based catalysts. In: Sustainable Catalysis: With Non-endangered Metals, Part 2. Cambridge: Royal Society of Chemistry; 2015. [citado 2024 jul. 07 ]
Artigo de periodico
Hard-templating of Prussian blue analogues in mesoporous silica and organosilica (2015)
Wang, Pei-Xi; Zamarion, Vitor de Moraes ; Hamad, Wadood Y; MacLachlan, Mark J
Source: Dalton Transactions. Unidade: IQ
Assunto: MATERIAIS NANOESTRUTURADOS
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ABNT
WANG, Pei-Xi et al. Hard-templating of Prussian blue analogues in mesoporous silica and organosilica. Dalton Transactions, v. 44, n. 33, p. 14724-14731, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5dt02213d. Acesso em: 07 jul. 2024.
APA
Wang, P. -X., Zamarion, V. de M., Hamad, W. Y., & MacLachlan, M. J. (2015). Hard-templating of Prussian blue analogues in mesoporous silica and organosilica. Dalton Transactions, 44( 33), 14724-14731. doi:10.1039/c5dt02213d
NLM
Wang P-X, Zamarion V de M, Hamad WY, MacLachlan MJ. Hard-templating of Prussian blue analogues in mesoporous silica and organosilica [Internet]. Dalton Transactions. 2015 ; 44( 33): 14724-14731.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5dt02213d
Vancouver
Wang P-X, Zamarion V de M, Hamad WY, MacLachlan MJ. Hard-templating of Prussian blue analogues in mesoporous silica and organosilica [Internet]. Dalton Transactions. 2015 ; 44( 33): 14724-14731.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5dt02213d
Artigo de periodico
Development and validation of a liquid chromatography method for anthocyanins in strawberry (Fragaria spp.) and complementary studies on stability, kinetics and antioxidant power (2015)
Canuto, Gisele André Baptista; Oliveira, Daniel Rossado; Conceição, Lucas S. M. da; Farah, João Pedro Simon ; Tavares, Marina Franco Maggi
Source: Food Chemistry. Unidade: IQ
Subjects: CROMATOGRAFIA LÍQUIDA, MORANGO, ANTIOXIDANTES
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ABNT
CANUTO, Gisele André Baptista et al. Development and validation of a liquid chromatography method for anthocyanins in strawberry (Fragaria spp.) and complementary studies on stability, kinetics and antioxidant power. Food Chemistry, v. 192, p. 566-574, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.foodchem.2015.06.095. Acesso em: 07 jul. 2024.
APA
Canuto, G. A. B., Oliveira, D. R., Conceição, L. S. M. da, Farah, J. P. S., & Tavares, M. F. M. (2015). Development and validation of a liquid chromatography method for anthocyanins in strawberry (Fragaria spp.) and complementary studies on stability, kinetics and antioxidant power. Food Chemistry, 192, 566-574. doi:10.1016/j.foodchem.2015.06.095
NLM
Canuto GAB, Oliveira DR, Conceição LSM da, Farah JPS, Tavares MFM. Development and validation of a liquid chromatography method for anthocyanins in strawberry (Fragaria spp.) and complementary studies on stability, kinetics and antioxidant power [Internet]. Food Chemistry. 2015 ; 192 566-574.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.foodchem.2015.06.095
Vancouver
Canuto GAB, Oliveira DR, Conceição LSM da, Farah JPS, Tavares MFM. Development and validation of a liquid chromatography method for anthocyanins in strawberry (Fragaria spp.) and complementary studies on stability, kinetics and antioxidant power [Internet]. Food Chemistry. 2015 ; 192 566-574.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.foodchem.2015.06.095
Artigo de periodico
Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols (2015)
Martins, Rodrigo S; Ahmad, Anees; Silva Junior, Luiz Fernando da; Andrade, Leandro Helgueira
Source: RSC Advances. Unidade: IQ
Subjects: LIPASE, SÍNTESE ORGÂNICA
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ABNT
MARTINS, Rodrigo S et al. Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols. RSC Advances, v. 5, n. 70, p. 56599-56605, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5ra06469d. Acesso em: 07 jul. 2024.
APA
Martins, R. S., Ahmad, A., Silva Junior, L. F. da, & Andrade, L. H. (2015). Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols. RSC Advances, 5( 70), 56599-56605. doi:10.1039/c5ra06469d
NLM
Martins RS, Ahmad A, Silva Junior LF da, Andrade LH. Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols [Internet]. RSC Advances. 2015 ; 5( 70): 56599-56605.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5ra06469d
Vancouver
Martins RS, Ahmad A, Silva Junior LF da, Andrade LH. Exploiting sequential lipase-catalyzed reactions to achieve enantiomerically pure chiral primary alcohols [Internet]. RSC Advances. 2015 ; 5( 70): 56599-56605.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5ra06469d
Artigo de periodico
Efficiency assessment of single unit monomer insertion reactions for monomer sequence control: kinetic simulations and experimental observations (2015)
Haven, Joris J; Vandenbergh, Joke; Kurita, Rafael; Gruber, Jonas ; Junkers, Thomas
Source: Polymer Chemistry. Unidade: IQ
Assunto: POLÍMEROS (QUÍMICA ORGÂNICA)
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HAVEN, Joris J et al. Efficiency assessment of single unit monomer insertion reactions for monomer sequence control: kinetic simulations and experimental observations. Polymer Chemistry, v. 6, n. 31, p. 5752-5765 : + Supplementary materials ( S1-S15), 2015Tradução . . Disponível em: https://doi.org/10.1039/c5py00485c. Acesso em: 07 jul. 2024.
APA
Haven, J. J., Vandenbergh, J., Kurita, R., Gruber, J., & Junkers, T. (2015). Efficiency assessment of single unit monomer insertion reactions for monomer sequence control: kinetic simulations and experimental observations. Polymer Chemistry, 6( 31), 5752-5765 : + Supplementary materials ( S1-S15). doi:10.1039/c5py00485c
NLM
Haven JJ, Vandenbergh J, Kurita R, Gruber J, Junkers T. Efficiency assessment of single unit monomer insertion reactions for monomer sequence control: kinetic simulations and experimental observations [Internet]. Polymer Chemistry. 2015 ; 6( 31): 5752-5765 : + Supplementary materials ( S1-S15).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5py00485c
Vancouver
Haven JJ, Vandenbergh J, Kurita R, Gruber J, Junkers T. Efficiency assessment of single unit monomer insertion reactions for monomer sequence control: kinetic simulations and experimental observations [Internet]. Polymer Chemistry. 2015 ; 6( 31): 5752-5765 : + Supplementary materials ( S1-S15).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5py00485c
Artigo de periodico
Electrochemical ecology: VIMP monitoring of plant defense against external stressors (2015)
Doménech-Carbó, Antonio; Cebrian Torreyon, Gerardo; Souto, Augusto Lopes; Moraes, Marcilio Martins de; Kato, Massuo Jorge ; Tavares, Josean Fechine; Barbosa Filho, José Maria
Source: RSC Advances. Unidade: IQ
Subjects: ELETROQUÍMICA, VOLTAMETRIA
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DOMÉNECH-CARBÓ, Antonio et al. Electrochemical ecology: VIMP monitoring of plant defense against external stressors. RSC Advances, v. 5, p. 61006-61011, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5ra11336a. Acesso em: 07 jul. 2024.
APA
Doménech-Carbó, A., Cebrian Torreyon, G., Souto, A. L., Moraes, M. M. de, Kato, M. J., Tavares, J. F., & Barbosa Filho, J. M. (2015). Electrochemical ecology: VIMP monitoring of plant defense against external stressors. RSC Advances, 5, 61006-61011. doi:10.1039/c5ra11336a
NLM
Doménech-Carbó A, Cebrian Torreyon G, Souto AL, Moraes MM de, Kato MJ, Tavares JF, Barbosa Filho JM. Electrochemical ecology: VIMP monitoring of plant defense against external stressors [Internet]. RSC Advances. 2015 ; 5 61006-61011.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5ra11336a
Vancouver
Doménech-Carbó A, Cebrian Torreyon G, Souto AL, Moraes MM de, Kato MJ, Tavares JF, Barbosa Filho JM. Electrochemical ecology: VIMP monitoring of plant defense against external stressors [Internet]. RSC Advances. 2015 ; 5 61006-61011.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c5ra11336a
Artigo de periodico
Electrophilic alkynylation of ketones using hypervalent iodine (2014)
Utaka, Aline; Cavalcanti, Livia N; Silva Junior, Luiz Fernando da
Source: Chemical Communications. Unidade: IQ
Subjects: COMPOSTOS ORGÂNICOS, QUÍMICA ORGÂNICA
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ABNT
UTAKA, Aline e CAVALCANTI, Livia N e SILVA JUNIOR, Luiz Fernando da. Electrophilic alkynylation of ketones using hypervalent iodine. Chemical Communications, v. 50, n. 29, p. 3810-3813, 2014Tradução . . Disponível em: https://doi.org/10.1039/c4cc00608a. Acesso em: 07 jul. 2024.
APA
Utaka, A., Cavalcanti, L. N., & Silva Junior, L. F. da. (2014). Electrophilic alkynylation of ketones using hypervalent iodine. Chemical Communications, 50( 29), 3810-3813. doi:10.1039/c4cc00608a
NLM
Utaka A, Cavalcanti LN, Silva Junior LF da. Electrophilic alkynylation of ketones using hypervalent iodine [Internet]. Chemical Communications. 2014 ; 50( 29): 3810-3813.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c4cc00608a
Vancouver
Utaka A, Cavalcanti LN, Silva Junior LF da. Electrophilic alkynylation of ketones using hypervalent iodine [Internet]. Chemical Communications. 2014 ; 50( 29): 3810-3813.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c4cc00608a
Artigo de periodico
Synthesis of L-cysteine-based boron compounds and their evaluation as proteasome inhibitors† (2014)
Milani, Priscila; Demasi, Marilene; Rezende, Leandro de; Amaral, Antonia Tavares do ; Andrade, Leandro Helgueira
Source: New Journal of Chemistry. Unidade: IQ
Subjects: BORO, LISOSSOMOS
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MILANI, Priscila et al. Synthesis of L-cysteine-based boron compounds and their evaluation as proteasome inhibitors†. New Journal of Chemistry, p. 3-15 : + Supplementary materials ( S1-S13), 2014Tradução . . Disponível em: https://doi.org/10.1039/c4nj00612g. Acesso em: 07 jul. 2024.
APA
Milani, P., Demasi, M., Rezende, L. de, Amaral, A. T. do, & Andrade, L. H. (2014). Synthesis of L-cysteine-based boron compounds and their evaluation as proteasome inhibitors†. New Journal of Chemistry, 3-15 : + Supplementary materials ( S1-S13). doi:10.1039/c4nj00612g
NLM
Milani P, Demasi M, Rezende L de, Amaral AT do, Andrade LH. Synthesis of L-cysteine-based boron compounds and their evaluation as proteasome inhibitors† [Internet]. New Journal of Chemistry. 2014 ; 3-15 : + Supplementary materials ( S1-S13).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c4nj00612g
Vancouver
Milani P, Demasi M, Rezende L de, Amaral AT do, Andrade LH. Synthesis of L-cysteine-based boron compounds and their evaluation as proteasome inhibitors† [Internet]. New Journal of Chemistry. 2014 ; 3-15 : + Supplementary materials ( S1-S13).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c4nj00612g
Artigo de periodico-divulgacao
Professor Alcindo A. dos Santos (Biography) (2014)
Santos, Alcindo Aparecido dos
Source: Tetrahedron. Unidade: IQ
Assunto: BIOGRAFIAS
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ABNT
SANTOS, Alcindo Aparecido dos. Professor Alcindo A. dos Santos (Biography). Tetrahedron. Oxford: Instituto de Química, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.tet.2014.03.077. Acesso em: 07 jul. 2024. , 2014
APA
Santos, A. A. dos. (2014). Professor Alcindo A. dos Santos (Biography). Tetrahedron. Oxford: Instituto de Química, Universidade de São Paulo. doi:10.1016/j.tet.2014.03.077
NLM
Santos AA dos. Professor Alcindo A. dos Santos (Biography) [Internet]. Tetrahedron. 2014 ; 70 3229.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tet.2014.03.077
Vancouver
Santos AA dos. Professor Alcindo A. dos Santos (Biography) [Internet]. Tetrahedron. 2014 ; 70 3229.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tet.2014.03.077
Trabalho de evento-resumo periodico
Pyridinium salts influence on lipid bilayers (2014)
Funari, Sérgio S; Di Vitta, Cláudio ; Marzorati, Liliana
Source: Biophysical Journal. Conference titles: Annual Meeting of the Biophysics Society. Unidade: IQ
Subjects: LIPÍDEOS, SAIS
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ABNT
FUNARI, Sérgio S e DI VITTA, Cláudio e MARZORATI, Liliana. Pyridinium salts influence on lipid bilayers. Biophysical Journal. Cambridge: Instituto de Química, Universidade de São Paulo. . Acesso em: 07 jul. 2024. , 2014
APA
Funari, S. S., Di Vitta, C., & Marzorati, L. (2014). Pyridinium salts influence on lipid bilayers. Biophysical Journal. Cambridge: Instituto de Química, Universidade de São Paulo.
NLM
Funari SS, Di Vitta C, Marzorati L. Pyridinium salts influence on lipid bilayers. Biophysical Journal. 2014 ; 106( 2): 90a res. 482.[citado 2024 jul. 07 ]
Vancouver
Funari SS, Di Vitta C, Marzorati L. Pyridinium salts influence on lipid bilayers. Biophysical Journal. 2014 ; 106( 2): 90a res. 482.[citado 2024 jul. 07 ]
Artigo de periodico
Ion jelly: a novel sensing material for gas sensors and electronic noses (2014)
Carvalho, Tânia; Vidinha, Pedro ; Vieira, Bruna Ricciardi; Li, Rosamaria Wu Chia; Gruber, Jonas
Source: Journal of Materials Chemistry C. Unidade: IQ
Subjects: LÍQUIDOS IÔNICOS, ELETROQUÍMICA, POLÍMEROS (QUÍMICA ORGÂNICA)
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CARVALHO, Tânia et al. Ion jelly: a novel sensing material for gas sensors and electronic noses. Journal of Materials Chemistry C, v. 2, n. 4, p. 696-700, 2014Tradução . . Disponível em: https://doi.org/10.1039/c3tc31496k. Acesso em: 07 jul. 2024.
APA
Carvalho, T., Vidinha, P., Vieira, B. R., Li, R. W. C., & Gruber, J. (2014). Ion jelly: a novel sensing material for gas sensors and electronic noses. Journal of Materials Chemistry C, 2( 4), 696-700. doi:10.1039/c3tc31496k
NLM
Carvalho T, Vidinha P, Vieira BR, Li RWC, Gruber J. Ion jelly: a novel sensing material for gas sensors and electronic noses [Internet]. Journal of Materials Chemistry C. 2014 ; 2( 4): 696-700.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c3tc31496k
Vancouver
Carvalho T, Vidinha P, Vieira BR, Li RWC, Gruber J. Ion jelly: a novel sensing material for gas sensors and electronic noses [Internet]. Journal of Materials Chemistry C. 2014 ; 2( 4): 696-700.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c3tc31496k
Artigo de periodico
Bromine and iodine-cucurbit[6]uril complexes: preparation and applications in synthetic organic chemistry (2014)
Reddy, Kishore Kumar Reddy Kachi; Cavallini, Thiago de Souza; Demets, Grégoire Jean-François; Silva Junior, Luiz Fernando da
Source: New Journal of Chemistry. Unidades: FFCLRP, IQ
Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS
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ABNT
REDDY, Kishore Kumar Reddy Kachi et al. Bromine and iodine-cucurbit[6]uril complexes: preparation and applications in synthetic organic chemistry. New Journal of Chemistry, v. 38, n. 6, p. 2262-2264 : + Supplementary materials ( S1-S35), 2014Tradução . . Disponível em: https://doi.org/10.1039/c4nj00284a. Acesso em: 07 jul. 2024.
APA
Reddy, K. K. R. K., Cavallini, T. de S., Demets, G. J. -F., & Silva Junior, L. F. da. (2014). Bromine and iodine-cucurbit[6]uril complexes: preparation and applications in synthetic organic chemistry. New Journal of Chemistry, 38( 6), 2262-2264 : + Supplementary materials ( S1-S35). doi:10.1039/c4nj00284a
NLM
Reddy KKRK, Cavallini T de S, Demets GJ-F, Silva Junior LF da. Bromine and iodine-cucurbit[6]uril complexes: preparation and applications in synthetic organic chemistry [Internet]. New Journal of Chemistry. 2014 ; 38( 6): 2262-2264 : + Supplementary materials ( S1-S35).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c4nj00284a
Vancouver
Reddy KKRK, Cavallini T de S, Demets GJ-F, Silva Junior LF da. Bromine and iodine-cucurbit[6]uril complexes: preparation and applications in synthetic organic chemistry [Internet]. New Journal of Chemistry. 2014 ; 38( 6): 2262-2264 : + Supplementary materials ( S1-S35).[citado 2024 jul. 07 ] Available from: https://doi.org/10.1039/c4nj00284a
Artigo de periodico
Cytotoxic non-aromatic b-ring flavanones from Piper carniconnectivum C. DC (2014)
Freitas, Giovana C; Batista Jr., João Marcos; Franchi Junior, Gilberto C; Nowill, Alexandre E; Yamaguchi, Lydia Fumiko; Vilcachagua, Janaina Dantas; Favaro, Denize Cristina; Furlan, Maysa; Guimarães, Elsie Franklin; Jeffrey, Christopher S; Kato, Massuo Jorge
Source: Phytochemistry. Unidade: IQ
Subjects: FLAVONÓIDES, FITOQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FREITAS, Giovana C et al. Cytotoxic non-aromatic b-ring flavanones from Piper carniconnectivum C. DC. Phytochemistry, v. 97, n. 1, p. 81-87, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.phytochem.2013.10.012. Acesso em: 07 jul. 2024.
APA
Freitas, G. C., Batista Jr., J. M., Franchi Junior, G. C., Nowill, A. E., Yamaguchi, L. F., Vilcachagua, J. D., et al. (2014). Cytotoxic non-aromatic b-ring flavanones from Piper carniconnectivum C. DC. Phytochemistry, 97( 1), 81-87. doi:10.1016/j.phytochem.2013.10.012
NLM
Freitas GC, Batista Jr. JM, Franchi Junior GC, Nowill AE, Yamaguchi LF, Vilcachagua JD, Favaro DC, Furlan M, Guimarães EF, Jeffrey CS, Kato MJ. Cytotoxic non-aromatic b-ring flavanones from Piper carniconnectivum C. DC [Internet]. Phytochemistry. 2014 ; 97( 1): 81-87.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.phytochem.2013.10.012
Vancouver
Freitas GC, Batista Jr. JM, Franchi Junior GC, Nowill AE, Yamaguchi LF, Vilcachagua JD, Favaro DC, Furlan M, Guimarães EF, Jeffrey CS, Kato MJ. Cytotoxic non-aromatic b-ring flavanones from Piper carniconnectivum C. DC [Internet]. Phytochemistry. 2014 ; 97( 1): 81-87.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.phytochem.2013.10.012
Artigo de periodico
Age-dependent changes from allylphenol to prenylated benzoic acid production in Piper gaudichaudianum Kunth (2014)
Gaia, Anderson Melo; Yamaguchi, Lydia Fumiko; Jeffrey, Christopher S; Kato, Massuo Jorge
Source: Phytochemistry. Unidade: IQ
Subjects: ONTOGENIA, FITOQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GAIA, Anderson Melo et al. Age-dependent changes from allylphenol to prenylated benzoic acid production in Piper gaudichaudianum Kunth. Phytochemistry, v. 106, p. 86-93, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.phytochem.2014.06.013. Acesso em: 07 jul. 2024.
APA
Gaia, A. M., Yamaguchi, L. F., Jeffrey, C. S., & Kato, M. J. (2014). Age-dependent changes from allylphenol to prenylated benzoic acid production in Piper gaudichaudianum Kunth. Phytochemistry, 106, 86-93. doi:10.1016/j.phytochem.2014.06.013
NLM
Gaia AM, Yamaguchi LF, Jeffrey CS, Kato MJ. Age-dependent changes from allylphenol to prenylated benzoic acid production in Piper gaudichaudianum Kunth [Internet]. Phytochemistry. 2014 ; 106 86-93.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.phytochem.2014.06.013
Vancouver
Gaia AM, Yamaguchi LF, Jeffrey CS, Kato MJ. Age-dependent changes from allylphenol to prenylated benzoic acid production in Piper gaudichaudianum Kunth [Internet]. Phytochemistry. 2014 ; 106 86-93.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.phytochem.2014.06.013
Artigo de periodico
New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices (2014)
Núñez, Cristina; Diniz, Mário; Santos, Alcindo Aparecido dos ; Capelo, José Luis; Lodeiro, Carlos
Source: Dyes and Pigments. Unidade: IQ
Subjects: FLUORESCÊNCIA, MERCÚRIO (ELEMENTO QUÍMICO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NÚÑEZ, Cristina et al. New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices. Dyes and Pigments, v. 101, p. 156-163, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2013.09.019. Acesso em: 07 jul. 2024.
APA
Núñez, C., Diniz, M., Santos, A. A. dos, Capelo, J. L., & Lodeiro, C. (2014). New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices. Dyes and Pigments, 101, 156-163. doi:10.1016/j.dyepig.2013.09.019
NLM
Núñez C, Diniz M, Santos AA dos, Capelo JL, Lodeiro C. New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices [Internet]. Dyes and Pigments. 2014 ; 101 156-163.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2013.09.019
Vancouver
Núñez C, Diniz M, Santos AA dos, Capelo JL, Lodeiro C. New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices [Internet]. Dyes and Pigments. 2014 ; 101 156-163.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2013.09.019
Artigo de periodico
On the thermal pummerer rearrangement of substituted sulfoxides (2014)
Marzorati, Liliana ; Yoshikawa, Eduardo Kunio Chinone; Braga, Ataualpa Albert Carmo ; Di Vitta, Cláudio
Source: Journal of Sulfur Chemistry. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARZORATI, Liliana et al. On the thermal pummerer rearrangement of substituted sulfoxides. Journal of Sulfur Chemistry, v. 35, n. 3, p. 248-260, 2014Tradução . . Disponível em: https://doi.org/10.1080/17415993.2013.853066. Acesso em: 07 jul. 2024.
APA
Marzorati, L., Yoshikawa, E. K. C., Braga, A. A. C., & Di Vitta, C. (2014). On the thermal pummerer rearrangement of substituted sulfoxides. Journal of Sulfur Chemistry, 35( 3), 248-260. doi:10.1080/17415993.2013.853066
NLM
Marzorati L, Yoshikawa EKC, Braga AAC, Di Vitta C. On the thermal pummerer rearrangement of substituted sulfoxides [Internet]. Journal of Sulfur Chemistry. 2014 ; 35( 3): 248-260.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1080/17415993.2013.853066
Vancouver
Marzorati L, Yoshikawa EKC, Braga AAC, Di Vitta C. On the thermal pummerer rearrangement of substituted sulfoxides [Internet]. Journal of Sulfur Chemistry. 2014 ; 35( 3): 248-260.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1080/17415993.2013.853066

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