ReP USP - Resultado da busca

Trabalho de evento-resumo
Cyclofunctionalizations using iodine/iodine(III) (2017)
Scarassati Filho, Paulo; Silva Junior, Luiz Fernando da
Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SCARASSATI FILHO, Paulo e SILVA JUNIOR, Luiz Fernando da. Cyclofunctionalizations using iodine/iodine(III). 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 03 nov. 2024.
APA
Scarassati Filho, P., & Silva Junior, L. F. da. (2017). Cyclofunctionalizations using iodine/iodine(III). In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Scarassati Filho P, Silva Junior LF da. Cyclofunctionalizations using iodine/iodine(III) [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Scarassati Filho P, Silva Junior LF da. Cyclofunctionalizations using iodine/iodine(III) [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Synthesis, stability study and biological application of organotelluranes (2017)
Princival, Cleverson Rogério; Predebon, Gabriela M; Archilha, Marcos Vinicio Lopes Rodrigues; Santos, Alcindo Aparecido dos ; Fernandes, Maria José Silva; Cunha, Rodrigo Luiz Oliveira Rodrigues; Comasseto, João Valdir
Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ
Subjects: COMPOSTOS ORGÂNICOS, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PRINCIVAL, Cleverson Rogério et al. Synthesis, stability study and biological application of organotelluranes. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 03 nov. 2024.
APA
Princival, C. R., Predebon, G. M., Archilha, M. V. L. R., Santos, A. A. dos, Fernandes, M. J. S., Cunha, R. L. O. R., & Comasseto, J. V. (2017). Synthesis, stability study and biological application of organotelluranes. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Princival CR, Predebon GM, Archilha MVLR, Santos AA dos, Fernandes MJS, Cunha RLOR, Comasseto JV. Synthesis, stability study and biological application of organotelluranes [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Princival CR, Predebon GM, Archilha MVLR, Santos AA dos, Fernandes MJS, Cunha RLOR, Comasseto JV. Synthesis, stability study and biological application of organotelluranes [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Toward the total synthesis of (+)-cis-trikentrin A (2017)
Lussari, Natália Vale; Tébéka, Iris Raquel Maia; Silva Junior, Luiz Fernando da
Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LUSSARI, Natália Vale e TÉBÉKA, Iris Raquel Maia e SILVA JUNIOR, Luiz Fernando da. Toward the total synthesis of (+)-cis-trikentrin A. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 03 nov. 2024.
APA
Lussari, N. V., Tébéka, I. R. M., & Silva Junior, L. F. da. (2017). Toward the total synthesis of (+)-cis-trikentrin A. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Lussari NV, Tébéka IRM, Silva Junior LF da. Toward the total synthesis of (+)-cis-trikentrin A [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Lussari NV, Tébéka IRM, Silva Junior LF da. Toward the total synthesis of (+)-cis-trikentrin A [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Theoretical study of the Pd-catalyzed O-methyl-N-phenilcarbamate direct arylation (2017)
Watanabe, Daniel Gianfranco; Braga, Ataualpa Albert Carmo
Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WATANABE, Daniel Gianfranco e BRAGA, Ataualpa Albert Carmo. Theoretical study of the Pd-catalyzed O-methyl-N-phenilcarbamate direct arylation. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 03 nov. 2024.
APA
Watanabe, D. G., & Braga, A. A. C. (2017). Theoretical study of the Pd-catalyzed O-methyl-N-phenilcarbamate direct arylation. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Watanabe DG, Braga AAC. Theoretical study of the Pd-catalyzed O-methyl-N-phenilcarbamate direct arylation [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Watanabe DG, Braga AAC. Theoretical study of the Pd-catalyzed O-methyl-N-phenilcarbamate direct arylation [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Studies toward asymmetric total synthesis of Raputindole D (2017)
Utaka, Aline; Silva Junior, Luiz Fernando da
Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ
Subjects: ALCALOIDES, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
UTAKA, Aline e SILVA JUNIOR, Luiz Fernando da. Studies toward asymmetric total synthesis of Raputindole D. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 03 nov. 2024.
APA
Utaka, A., & Silva Junior, L. F. da. (2017). Studies toward asymmetric total synthesis of Raputindole D. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Utaka A, Silva Junior LF da. Studies toward asymmetric total synthesis of Raputindole D [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Utaka A, Silva Junior LF da. Studies toward asymmetric total synthesis of Raputindole D [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
DFT elucidation of regio- and enantioselective Heck arylation using acyclic olefins and aryldiazonium salts as substrates (2017)
Silva, Vitor Hugo Menezes da; Oliveira, Caio Cesar Spindola de; Correia, Carlos Roque Duarte; Braga, Ataualpa Albert Carmo
Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Vitor Hugo Menezes da et al. DFT elucidation of regio- and enantioselective Heck arylation using acyclic olefins and aryldiazonium salts as substrates. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 03 nov. 2024.
APA
Silva, V. H. M. da, Oliveira, C. C. S. de, Correia, C. R. D., & Braga, A. A. C. (2017). DFT elucidation of regio- and enantioselective Heck arylation using acyclic olefins and aryldiazonium salts as substrates. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Silva VHM da, Oliveira CCS de, Correia CRD, Braga AAC. DFT elucidation of regio- and enantioselective Heck arylation using acyclic olefins and aryldiazonium salts as substrates [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Silva VHM da, Oliveira CCS de, Correia CRD, Braga AAC. DFT elucidation of regio- and enantioselective Heck arylation using acyclic olefins and aryldiazonium salts as substrates [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Artigo de periodico
3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions (2017)
Vasconcelos, Stanley N. S; Silva, Vitor Hugo Menezes da; Braga, Ataualpa Albert Carmo ; Shamim, Anwar; Souza, Frederico B; Pimenta, Daniel C; Stefani, Hélio Alexandre
Source: Asian Journal Organic of Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VASCONCELOS, Stanley N. S et al. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, v. 6, n. 7, p. 913-920, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajoc.201700154. Acesso em: 03 nov. 2024.
APA
Vasconcelos, S. N. S., Silva, V. H. M. da, Braga, A. A. C., Shamim, A., Souza, F. B., Pimenta, D. C., & Stefani, H. A. (2017). 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, 6( 7), 913-920. doi:10.1002/ajoc.201700154
NLM
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/ajoc.201700154
Vancouver
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/ajoc.201700154
Trabalho de evento-resumo
3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions (2017)
Vasconcelos, Stanley Nunes Siqueira; Silva, Vitor Hugo Menezes da; Braga, Ataualpa Albert Carmo ; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Abstracts. Conference titles: Tetrahedron Symposium - New Development in Organic Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. 2017, Anais.. Budapest: Elsevier, 2017. . Acesso em: 03 nov. 2024.
APA
Vasconcelos, S. N. S., Silva, V. H. M. da, Braga, A. A. C., Pimenta, D. C., & Stefani, H. A. (2017). 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. In Abstracts. Budapest: Elsevier.
NLM
Vasconcelos SNS, Silva VHM da, Braga AAC, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Abstracts. 2017 ;[citado 2024 nov. 03 ]
Vancouver
Vasconcelos SNS, Silva VHM da, Braga AAC, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Abstracts. 2017 ;[citado 2024 nov. 03 ]
Artigo de periodico
Lipid Matrices destabilization induced by some newly synthesized pyridinium salts (2017)
Luchese, Angelica M; Di Vitta, Cláudio ; Marzorati, Liliana ; Yamaoka , Patrícia; Funari, Sérgio S
Source: ChemistrySelect. Unidade: IQ
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LUCHESE, Angelica M et al. Lipid Matrices destabilization induced by some newly synthesized pyridinium salts. ChemistrySelect, v. 2, n. 4, p. 1491-1496, 2017Tradução . . Disponível em: https://doi.org/10.1002/slct.201601588. Acesso em: 03 nov. 2024.
APA
Luchese, A. M., Di Vitta, C., Marzorati, L., Yamaoka , P., & Funari, S. S. (2017). Lipid Matrices destabilization induced by some newly synthesized pyridinium salts. ChemistrySelect, 2( 4), 1491-1496. doi:10.1002/slct.201601588
NLM
Luchese AM, Di Vitta C, Marzorati L, Yamaoka P, Funari SS. Lipid Matrices destabilization induced by some newly synthesized pyridinium salts [Internet]. ChemistrySelect. 2017 ; 2( 4): 1491-1496.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/slct.201601588
Vancouver
Luchese AM, Di Vitta C, Marzorati L, Yamaoka P, Funari SS. Lipid Matrices destabilization induced by some newly synthesized pyridinium salts [Internet]. ChemistrySelect. 2017 ; 2( 4): 1491-1496.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/slct.201601588
Artigo de periodico
Iron-catalyzed synthesis of oxindoles: application to the preparation of pyrroloindolines (2017)
Correia, Valquírio G; Abreu, Juliana C; Barata, Caio A. E; Andrade, Leandro Helgueira
Source: Organic Letters. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, ALCALOIDES DE PIRROLIZIDINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CORREIA, Valquírio G et al. Iron-catalyzed synthesis of oxindoles: application to the preparation of pyrroloindolines. Organic Letters, v. 19, n. 5, p. 1060-1063, 2017Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.7b00078. Acesso em: 03 nov. 2024.
APA
Correia, V. G., Abreu, J. C., Barata, C. A. E., & Andrade, L. H. (2017). Iron-catalyzed synthesis of oxindoles: application to the preparation of pyrroloindolines. Organic Letters, 19( 5), 1060-1063. doi:10.1021/acs.orglett.7b00078
NLM
Correia VG, Abreu JC, Barata CAE, Andrade LH. Iron-catalyzed synthesis of oxindoles: application to the preparation of pyrroloindolines [Internet]. Organic Letters. 2017 ; 19( 5): 1060-1063.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1021/acs.orglett.7b00078
Vancouver
Correia VG, Abreu JC, Barata CAE, Andrade LH. Iron-catalyzed synthesis of oxindoles: application to the preparation of pyrroloindolines [Internet]. Organic Letters. 2017 ; 19( 5): 1060-1063.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1021/acs.orglett.7b00078
Trabalho de evento-resumo
Highly selective deoxygenation of epoxides over magnetically recoverable gold catalyst (2017)
Fiorio, Jhonatan Luiz; Rossi, Liane Marcia
Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FIORIO, Jhonatan Luiz e ROSSI, Liane Marcia. Highly selective deoxygenation of epoxides over magnetically recoverable gold catalyst. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 03 nov. 2024.
APA
Fiorio, J. L., & Rossi, L. M. (2017). Highly selective deoxygenation of epoxides over magnetically recoverable gold catalyst. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Fiorio JL, Rossi LM. Highly selective deoxygenation of epoxides over magnetically recoverable gold catalyst [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Fiorio JL, Rossi LM. Highly selective deoxygenation of epoxides over magnetically recoverable gold catalyst [Internet]. Proceedings. 2017 ;[citado 2024 nov. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Artigo de periodico
Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines (2017)
Oliveira, Isadora M. de; Vasconcelos, Stanley S. N; Barbeiro, Cristiane S; Correra, Thiago Carita ; Shamim, Anwar; Pimenta, Daniel Carvalho; Caracelli, Ignez; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: New Journal of Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, REAÇÕES ORGÂNICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Isadora M. de et al. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, v. 41, p. 9884-9888, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7nj01803g. Acesso em: 03 nov. 2024.
APA
Oliveira, I. M. de, Vasconcelos, S. S. N., Barbeiro, C. S., Correra, T. C., Shamim, A., Pimenta, D. C., et al. (2017). Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, 41, 9884-9888. doi:10.1039/c7nj01803g
NLM
Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1039/c7nj01803g
Vancouver
Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1039/c7nj01803g

USP Schools

ReP

Filtros

Authors

USP affiliated authors

Subjects

Source title

Grupo de pesquisa

Normalized affiliation