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BORTOLETTO, Aline Marques; SILVELLO, Giovanni Casagrande; ALCARDE, André Ricardo. Aromatic profiling of flavor active compounds in sugarcane spirits aged in tropical wooden barrels. Brazilian Journal of Food Technology, Campinas, v. 24, p. 1-14, 2021. Disponível em: < https://www.scielo.br/j/bjft/a/8fNh6v5HQ59RfdNY6BvK3kn/?lang=en > DOI: doi.org/10.1590/1981-6723.07119.
APA
Bortoletto, A. M., Silvello, G. C., & Alcarde, A. R. (2021). Aromatic profiling of flavor active compounds in sugarcane spirits aged in tropical wooden barrels. Brazilian Journal of Food Technology, 24, 1-14. doi:doi.org/10.1590/1981-6723.07119
NLM
Bortoletto AM, Silvello GC, Alcarde AR. Aromatic profiling of flavor active compounds in sugarcane spirits aged in tropical wooden barrels [Internet]. Brazilian Journal of Food Technology. 2021 ; 24 1-14.Available from: https://www.scielo.br/j/bjft/a/8fNh6v5HQ59RfdNY6BvK3kn/?lang=en
Vancouver
Bortoletto AM, Silvello GC, Alcarde AR. Aromatic profiling of flavor active compounds in sugarcane spirits aged in tropical wooden barrels [Internet]. Brazilian Journal of Food Technology. 2021 ; 24 1-14.Available from: https://www.scielo.br/j/bjft/a/8fNh6v5HQ59RfdNY6BvK3kn/?lang=en
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SANABRIA, Marialy Nieves; ANDRADE, Leandro Helgueira. Microwave irradiation and formamide: a perfect match for ultrafast carbamoylation via radical reactions. ACS Sustainable Chemistry & Engineering, Washington, v. 9, n. 41, p. 13735-13741, 2021. Disponível em: < https://dx.doi.org/10.1021/acssuschemeng.1c04077 > DOI: 10.1021/acssuschemeng.1c04077.
APA
Sanabria, M. N., & Andrade, L. H. (2021). Microwave irradiation and formamide: a perfect match for ultrafast carbamoylation via radical reactions. ACS Sustainable Chemistry & Engineering, 9( 41), 13735-13741. doi:10.1021/acssuschemeng.1c04077
NLM
Sanabria MN, Andrade LH. Microwave irradiation and formamide: a perfect match for ultrafast carbamoylation via radical reactions [Internet]. ACS Sustainable Chemistry & Engineering. 2021 ; 9( 41): 13735-13741.Available from: https://dx.doi.org/10.1021/acssuschemeng.1c04077
Vancouver
Sanabria MN, Andrade LH. Microwave irradiation and formamide: a perfect match for ultrafast carbamoylation via radical reactions [Internet]. ACS Sustainable Chemistry & Engineering. 2021 ; 9( 41): 13735-13741.Available from: https://dx.doi.org/10.1021/acssuschemeng.1c04077
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MURIE, Valter Eduardo; NICOLINO, Paula Valim; SANTOS, Thiago dos; et al. Synthesis of 7-Chloroquinoline derivatives using mixed Lithium-Magnesium reagents. The Journal of Organic Chemistry, Washington, p. 1-8, 2021. Disponível em: < https://doi.org/10.1021/acs.joc.1c01521 > DOI: 10.1021/acs.joc.1c01521.
APA
Murie, V. E., Nicolino, P. V., Santos, T. dos, Gambacorta, G., Nishimura, R. H. V., Perovani, I. S., et al. (2021). Synthesis of 7-Chloroquinoline derivatives using mixed Lithium-Magnesium reagents. The Journal of Organic Chemistry, 1-8. doi:10.1021/acs.joc.1c01521
NLM
Murie VE, Nicolino PV, Santos T dos, Gambacorta G, Nishimura RHV, Perovani IS, Furtado LC, Lotufo LVC, Oliveira ARM de, Lourenço RV, Baxendale IR, Clososki GC. Synthesis of 7-Chloroquinoline derivatives using mixed Lithium-Magnesium reagents [Internet]. The Journal of Organic Chemistry. 2021 ; 1-8.Available from: https://doi.org/10.1021/acs.joc.1c01521
Vancouver
Murie VE, Nicolino PV, Santos T dos, Gambacorta G, Nishimura RHV, Perovani IS, Furtado LC, Lotufo LVC, Oliveira ARM de, Lourenço RV, Baxendale IR, Clososki GC. Synthesis of 7-Chloroquinoline derivatives using mixed Lithium-Magnesium reagents [Internet]. The Journal of Organic Chemistry. 2021 ; 1-8.Available from: https://doi.org/10.1021/acs.joc.1c01521
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GARCIA, Rafael de Queiroz; DE BONI, Leonardo. Espectroscopia ultrarrápida: excitação e prova degenerados e não degenerados resolvidos em polarização. Anais.. São Carlos: Instituto de Física de São Carlos - IFSC, 2021.
APA
Garcia, R. de Q., & De Boni, L. (2021). Espectroscopia ultrarrápida: excitação e prova degenerados e não degenerados resolvidos em polarização. In Livro de Resumos. São Carlos: Instituto de Física de São Carlos - IFSC.
NLM
Garcia R de Q, De Boni L. Espectroscopia ultrarrápida: excitação e prova degenerados e não degenerados resolvidos em polarização. Livro de Resumos. 2021 ;
Vancouver
Garcia R de Q, De Boni L. Espectroscopia ultrarrápida: excitação e prova degenerados e não degenerados resolvidos em polarização. Livro de Resumos. 2021 ;
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PASCHOAL, Vitor Hugo; RIBEIRO, Mauro Carlos Costa. Structure and dynamics of aromatic and alkyl substituted Imidazolium-based ionic liquids. Journal of Molecular Liquids, Amsterdam, v. 340, p. 1-9 art. 117285, 2021. Disponível em: < https://dx.doi.org/10.1016/j.molliq.2021.117285 > DOI: 10.1016/j.molliq.2021.117285.
APA
Paschoal, V. H., & Ribeiro, M. C. C. (2021). Structure and dynamics of aromatic and alkyl substituted Imidazolium-based ionic liquids. Journal of Molecular Liquids, 340, 1-9 art. 117285. doi:10.1016/j.molliq.2021.117285
NLM
Paschoal VH, Ribeiro MCC. Structure and dynamics of aromatic and alkyl substituted Imidazolium-based ionic liquids [Internet]. Journal of Molecular Liquids. 2021 ; 340 1-9 art. 117285.Available from: https://dx.doi.org/10.1016/j.molliq.2021.117285
Vancouver
Paschoal VH, Ribeiro MCC. Structure and dynamics of aromatic and alkyl substituted Imidazolium-based ionic liquids [Internet]. Journal of Molecular Liquids. 2021 ; 340 1-9 art. 117285.Available from: https://dx.doi.org/10.1016/j.molliq.2021.117285
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GARCIA, Ellen Cristine Duarte; FORNAZIERI, Marco Aurelio; ROSSANEIS, Ana Carolina; et al. Safety and efficacy of superior turbinate biopsies as a source of olfactory epithelium appropriate for morphological analysis. European archives of oto-rhino-laryngology, New York, v. 277, n. 2, p. 483-492, 2020. Disponível em: < https://observatorio.fm.usp.br/handle/OPI/36014 > DOI: 10.1007/s00405-019-05728-7.
APA
Garcia, E. C. D., Fornazieri, M. A., Rossaneis, A. C., Pipino, A. S., Gomes, G. V., Pinna, F. D. R., et al. (2020). Safety and efficacy of superior turbinate biopsies as a source of olfactory epithelium appropriate for morphological analysis. European archives of oto-rhino-laryngology, 277( 2), 483-492. doi:10.1007/s00405-019-05728-7
NLM
Garcia ECD, Fornazieri MA, Rossaneis AC, Pipino AS, Gomes GV, Pinna FDR, Voegels RL, Doty RL, Verri WA. Safety and efficacy of superior turbinate biopsies as a source of olfactory epithelium appropriate for morphological analysis [Internet]. European archives of oto-rhino-laryngology. 2020 ; 277( 2): 483-492.Available from: https://observatorio.fm.usp.br/handle/OPI/36014
Vancouver
Garcia ECD, Fornazieri MA, Rossaneis AC, Pipino AS, Gomes GV, Pinna FDR, Voegels RL, Doty RL, Verri WA. Safety and efficacy of superior turbinate biopsies as a source of olfactory epithelium appropriate for morphological analysis [Internet]. European archives of oto-rhino-laryngology. 2020 ; 277( 2): 483-492.Available from: https://observatorio.fm.usp.br/handle/OPI/36014
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YANG, Ni; GALVES, Cassia; GONÇALVES, Ana Carolina Racioni; CHEN, Jianshe; FISK, Ian. Impact of capsaicin on aroma release: in vitro and in vivo analysis. Food Research International, Amsterdam, v. 133, p. 1-9, 2020. Disponível em: < https://doi.org/10.1016/j.foodres.2020.109197 > DOI: 10.1016/j.foodres.2020.109197.
APA
Yang, N., Galves, C., Gonçalves, A. C. R., Chen, J., & Fisk, I. (2020). Impact of capsaicin on aroma release: in vitro and in vivo analysis. Food Research International, 133, 1-9. doi:10.1016/j.foodres.2020.109197
NLM
Yang N, Galves C, Gonçalves ACR, Chen J, Fisk I. Impact of capsaicin on aroma release: in vitro and in vivo analysis [Internet]. Food Research International. 2020 ; 133 1-9.Available from: https://doi.org/10.1016/j.foodres.2020.109197
Vancouver
Yang N, Galves C, Gonçalves ACR, Chen J, Fisk I. Impact of capsaicin on aroma release: in vitro and in vivo analysis [Internet]. Food Research International. 2020 ; 133 1-9.Available from: https://doi.org/10.1016/j.foodres.2020.109197
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BONFIM, Caroline Measso do; MONTELEONI, Letícia Figueiredo; CALMONA, Marília de Freitas; et al. Antiviral activity of curcumin-nanoemulsion associated with photodynamic therapy in vulvar cell lines transducing different variants of HPV-16. Artificial Cells, Nanomedicine and Biotechnology, Philadelphia, v. 48, n. 1, p. 515-524, 2020. Disponível em: < https://doi.org/10.1080/21691401.2020.1725023 > DOI: 10.1080/21691401.2020.1725023.
APA
Bonfim, C. M. do, Monteleoni, L. F., Calmona, M. de F., Cândido, N. M., Provazzi, P. J. S., Lino, V. de S., et al. (2020). Antiviral activity of curcumin-nanoemulsion associated with photodynamic therapy in vulvar cell lines transducing different variants of HPV-16. Artificial Cells, Nanomedicine and Biotechnology, 48( 1), 515-524. doi:10.1080/21691401.2020.1725023
NLM
Bonfim CM do, Monteleoni LF, Calmona M de F, Cândido NM, Provazzi PJS, Lino V de S, Rabachini T, Sichero L, Villa LL, Quintana SM, Melli PP dos S, Primo FL, Amantino CF, Tedesco AC, Pierulivo EMB, Rahal P. Antiviral activity of curcumin-nanoemulsion associated with photodynamic therapy in vulvar cell lines transducing different variants of HPV-16 [Internet]. Artificial Cells, Nanomedicine and Biotechnology. 2020 ; 48( 1): 515-524.Available from: https://doi.org/10.1080/21691401.2020.1725023
Vancouver
Bonfim CM do, Monteleoni LF, Calmona M de F, Cândido NM, Provazzi PJS, Lino V de S, Rabachini T, Sichero L, Villa LL, Quintana SM, Melli PP dos S, Primo FL, Amantino CF, Tedesco AC, Pierulivo EMB, Rahal P. Antiviral activity of curcumin-nanoemulsion associated with photodynamic therapy in vulvar cell lines transducing different variants of HPV-16 [Internet]. Artificial Cells, Nanomedicine and Biotechnology. 2020 ; 48( 1): 515-524.Available from: https://doi.org/10.1080/21691401.2020.1725023
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MARTINS, Júlia; COELHO, Joana; TADINI, Maraine Catarina; et al. Yangambin and Epi-yangambin isomers: new purification method from Ocotea fasciculata and first cytotoxic aspects focusing on In Vivo safety. Planta Medica, Stuttgart, v. 86, p. 415-424, 2020. Disponível em: < https://doi.org/10.1055/a-1118-3828 > DOI: 10.1055/a-1118-3828.
APA
Martins, J., Coelho, J., Tadini, M. C., Souza, R. O. de, Figueiredo, S. A., Fonseca, M. J. V., et al. (2020). Yangambin and Epi-yangambin isomers: new purification method from Ocotea fasciculata and first cytotoxic aspects focusing on In Vivo safety. Planta Medica, 86, 415-424. doi:10.1055/a-1118-3828
NLM
Martins J, Coelho J, Tadini MC, Souza RO de, Figueiredo SA, Fonseca MJV, Albuquerque NCP de, Lopes NP, Berretta AA, Marquele-Oliveira F, Oliveira ARM de. Yangambin and Epi-yangambin isomers: new purification method from Ocotea fasciculata and first cytotoxic aspects focusing on In Vivo safety [Internet]. Planta Medica. 2020 ; 86 415-424.Available from: https://doi.org/10.1055/a-1118-3828
Vancouver
Martins J, Coelho J, Tadini MC, Souza RO de, Figueiredo SA, Fonseca MJV, Albuquerque NCP de, Lopes NP, Berretta AA, Marquele-Oliveira F, Oliveira ARM de. Yangambin and Epi-yangambin isomers: new purification method from Ocotea fasciculata and first cytotoxic aspects focusing on In Vivo safety [Internet]. Planta Medica. 2020 ; 86 415-424.Available from: https://doi.org/10.1055/a-1118-3828
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OLIVEIRA, Marilene Silva; JOSE PEDRO, Friedmann Angeli; AQUINO, Gilberto L. B; et al. Heck reaction synthesis of anthracene and naphthalene derivatives as traps and clean chemical sources of singlet molecular oxygen in biological systems. Photochemical and Photobiological Sciences, Cambridge, v. 19, p. 1590-1602, 2020. Disponível em: < http://dx.doi.org>10.1039/d0pp00153h > DOI: 10.1039/d0pp00153h.
APA
Oliveira, M. S., Jose Pedro, F. A., Aquino, G. L. B., Ronsein, G. E., Oliveira, M. C. B. de, Barbosa, L. F., et al. (2020). Heck reaction synthesis of anthracene and naphthalene derivatives as traps and clean chemical sources of singlet molecular oxygen in biological systems. Photochemical and Photobiological Sciences, 19, 1590-1602. doi:10.1039/d0pp00153h
NLM
Oliveira MS, Jose Pedro FA, Aquino GLB, Ronsein GE, Oliveira MCB de, Barbosa LF, Medeiros MHG de, Greer A, Di Mascio P, Chorociejus G. Heck reaction synthesis of anthracene and naphthalene derivatives as traps and clean chemical sources of singlet molecular oxygen in biological systems [Internet]. Photochemical and Photobiological Sciences. 2020 ; 19 1590-1602.Available from: http://dx.doi.org>10.1039/d0pp00153h
Vancouver
Oliveira MS, Jose Pedro FA, Aquino GLB, Ronsein GE, Oliveira MCB de, Barbosa LF, Medeiros MHG de, Greer A, Di Mascio P, Chorociejus G. Heck reaction synthesis of anthracene and naphthalene derivatives as traps and clean chemical sources of singlet molecular oxygen in biological systems [Internet]. Photochemical and Photobiological Sciences. 2020 ; 19 1590-1602.Available from: http://dx.doi.org>10.1039/d0pp00153h
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ALI, Arif; KHALID, Muhammad; REHMAN, Muhammad Fayyaz ur; et al. Efficient synthesis, SC-XRD, and theoretical studies of О-Benzenesulfonylated pyrimidines: role of noncovalent interaction influence in their supramolecular network. ACS Omega, Washington, v. 5, p. 15115−15128, 2020. Disponível em: < http://dx.doi.org/10.1021/acsomega.0c00975 > DOI: 10.1021/acsomega.0c00975.
APA
Ali, A., Khalid, M., Rehman, M. F. ur, Haq, S., Ali, A., Tahir, M. N., et al. (2020). Efficient synthesis, SC-XRD, and theoretical studies of О-Benzenesulfonylated pyrimidines: role of noncovalent interaction influence in their supramolecular network. ACS Omega, 5, 15115−15128. doi:10.1021/acsomega.0c00975
NLM
Ali A, Khalid M, Rehman MF ur, Haq S, Ali A, Tahir MN, Ashfaq M, Rasool F, Braga AAC. Efficient synthesis, SC-XRD, and theoretical studies of О-Benzenesulfonylated pyrimidines: role of noncovalent interaction influence in their supramolecular network [Internet]. ACS Omega. 2020 ; 5 15115−15128.Available from: http://dx.doi.org/10.1021/acsomega.0c00975
Vancouver
Ali A, Khalid M, Rehman MF ur, Haq S, Ali A, Tahir MN, Ashfaq M, Rasool F, Braga AAC. Efficient synthesis, SC-XRD, and theoretical studies of О-Benzenesulfonylated pyrimidines: role of noncovalent interaction influence in their supramolecular network [Internet]. ACS Omega. 2020 ; 5 15115−15128.Available from: http://dx.doi.org/10.1021/acsomega.0c00975
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KATIKI, Luciana Morita; FERREIRA, J. F. S; AMARANTE, A. F. T; et al. Evaluation of encapsulated anethole and carvone in lambs artificially and naturally-infected with Haemonchus contortus. Experimental Parasitology, Orlando, v. 197, p. 36-42, 2019. DOI: 10.1016/j.exppara.2019.01.002.
APA
Katiki, L. M., Ferreira, J. F. S., Amarante, A. F. T., Araujo, R. C. de, Ziegelmeyer, L., Gomes, A. C. P., et al. (2019). Evaluation of encapsulated anethole and carvone in lambs artificially and naturally-infected with Haemonchus contortus. Experimental Parasitology, 197, 36-42. doi:10.1016/j.exppara.2019.01.002
NLM
Katiki LM, Ferreira JFS, Amarante AFT, Araujo RC de, Ziegelmeyer L, Gomes ACP, Gutmanis G, Rodrigues L, Bueno MS, Veríssimo CJ, Louvandini H. Evaluation of encapsulated anethole and carvone in lambs artificially and naturally-infected with Haemonchus contortus. Experimental Parasitology. 2019 ; 197 36-42.
Vancouver
Katiki LM, Ferreira JFS, Amarante AFT, Araujo RC de, Ziegelmeyer L, Gomes ACP, Gutmanis G, Rodrigues L, Bueno MS, Veríssimo CJ, Louvandini H. Evaluation of encapsulated anethole and carvone in lambs artificially and naturally-infected with Haemonchus contortus. Experimental Parasitology. 2019 ; 197 36-42.
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DIAS, Felipe Morillo Sanz; GOMEZ, José Gregório Cabrera; SILVA, Luiziana Ferreira da. Construção de linhagens de Pseudomonas putida capazes de produzir compostos aromáticos por meio de vias metabólicas sintéticas. 2019.Universidade de São Paulo, São Paulo, 2019. Disponível em: < http://www.teses.usp.br/teses/disponiveis/87/87131/tde-13112019-114837/ >.
APA
Dias, F. M. S., Gomez, J. G. C., & Silva, L. F. da. (2019). Construção de linhagens de Pseudomonas putida capazes de produzir compostos aromáticos por meio de vias metabólicas sintéticas. Universidade de São Paulo, São Paulo. Recuperado de http://www.teses.usp.br/teses/disponiveis/87/87131/tde-13112019-114837/
NLM
Dias FMS, Gomez JGC, Silva LF da. Construção de linhagens de Pseudomonas putida capazes de produzir compostos aromáticos por meio de vias metabólicas sintéticas [Internet]. 2019 ;Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-13112019-114837/
Vancouver
Dias FMS, Gomez JGC, Silva LF da. Construção de linhagens de Pseudomonas putida capazes de produzir compostos aromáticos por meio de vias metabólicas sintéticas [Internet]. 2019 ;Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-13112019-114837/
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VILLELA-CASTRO, Diana Lima; SANTOS, Vera Lucia Conceição de Gouveia; WOO, Kevin. Polyhexanide versus metronidazole for odor management in malignant (fungating) wounds: a double-blinded, randomized, clinical trial. Journal of Wound, Ostomy, and Continence Nursing: official publication of The Wound, Ostomy and Continence Nurses Society, St. Louis, MO, v. 45, n. 5, p. 413-418, 2018. DOI: 10.1097/WON.0000000000000460.
APA
Villela-Castro, D. L., Santos, V. L. C. de G., & Woo, K. (2018). Polyhexanide versus metronidazole for odor management in malignant (fungating) wounds: a double-blinded, randomized, clinical trial. Journal of Wound, Ostomy, and Continence Nursing: official publication of The Wound, Ostomy and Continence Nurses Society, 45( 5), 413-418. doi:10.1097/WON.0000000000000460
NLM
Villela-Castro DL, Santos VLC de G, Woo K. Polyhexanide versus metronidazole for odor management in malignant (fungating) wounds: a double-blinded, randomized, clinical trial. Journal of Wound, Ostomy, and Continence Nursing: official publication of The Wound, Ostomy and Continence Nurses Society. 2018 ; 45( 5): 413-418.
Vancouver
Villela-Castro DL, Santos VLC de G, Woo K. Polyhexanide versus metronidazole for odor management in malignant (fungating) wounds: a double-blinded, randomized, clinical trial. Journal of Wound, Ostomy, and Continence Nursing: official publication of The Wound, Ostomy and Continence Nurses Society. 2018 ; 45( 5): 413-418.
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ARAÚJO, Thalita Macedo; SOUZA, Magalhães Teixeira; DINIZ, Raphael Hermano Santos; et al. Cachaça yeast strains: alternative starters to produce beer and bioethanol. Antonie van Leeuwenhoek, Wageningen, v. 111, n. 10, p. 1749-1766, 2018. Disponível em: < http://dx.doi.org/10.1007/s10482-018-1063-3 > DOI: 10.1007/s10482-018-1063-3.
APA
Araújo, T. M., Souza, M. T., Diniz, R. H. S., Yamakawa, C. K., Soares, L. B., Lenczak, J. L., et al. (2018). Cachaça yeast strains: alternative starters to produce beer and bioethanol. Antonie van Leeuwenhoek, 111( 10), 1749-1766. doi:10.1007/s10482-018-1063-3
NLM
Araújo TM, Souza MT, Diniz RHS, Yamakawa CK, Soares LB, Lenczak JL, Oliveira JV de C, Goldman GH, Barbosa EA, Campos ACS, Castro IM, Brandão RL. Cachaça yeast strains: alternative starters to produce beer and bioethanol [Internet]. Antonie van Leeuwenhoek. 2018 ; 111( 10): 1749-1766.Available from: http://dx.doi.org/10.1007/s10482-018-1063-3
Vancouver
Araújo TM, Souza MT, Diniz RHS, Yamakawa CK, Soares LB, Lenczak JL, Oliveira JV de C, Goldman GH, Barbosa EA, Campos ACS, Castro IM, Brandão RL. Cachaça yeast strains: alternative starters to produce beer and bioethanol [Internet]. Antonie van Leeuwenhoek. 2018 ; 111( 10): 1749-1766.Available from: http://dx.doi.org/10.1007/s10482-018-1063-3
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SILVA, Rodrigo M. da; GUARATINI, Thais; JIMENEZ, Paula C.; et al. Mass spectrometry analysis of protonated marine natural product seriniquinone. Journal Brazilian Chemical Society, São Paulo, v. 29, n. 5, p. 1162-1166, 2018. Disponível em: < http://dx.doi.org/10.21577/0103-5053.20180037 > DOI: 10.21577/0103-50353.20180037.
APA
Silva, R. M. da, Guaratini, T., Jimenez, P. C., Fenical, W., Vessecchi, R., Lopes, N. P., & Costa-Lotufo, L. V. (2018). Mass spectrometry analysis of protonated marine natural product seriniquinone. Journal Brazilian Chemical Society, 29( 5), 1162-1166. doi:10.21577/0103-50353.20180037
NLM
Silva RM da, Guaratini T, Jimenez PC, Fenical W, Vessecchi R, Lopes NP, Costa-Lotufo LV. Mass spectrometry analysis of protonated marine natural product seriniquinone [Internet]. Journal Brazilian Chemical Society. 2018 ; 29( 5): 1162-1166.Available from: http://dx.doi.org/10.21577/0103-5053.20180037
Vancouver
Silva RM da, Guaratini T, Jimenez PC, Fenical W, Vessecchi R, Lopes NP, Costa-Lotufo LV. Mass spectrometry analysis of protonated marine natural product seriniquinone [Internet]. Journal Brazilian Chemical Society. 2018 ; 29( 5): 1162-1166.Available from: http://dx.doi.org/10.21577/0103-5053.20180037
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CAUMO, Sofia Ellen da Silva; CUSTÓDIO, Danilo; VICENTE, Ana; ALVES, Célia; VASCONCELLOS, Pérola de Castro. Concentration of aliphatic and polycyclic aromatic compounds in atmospheric samples collected around a petrochemical site at São Paulo, Brazil. Anais.. São Paulo: Sociedade Brasileira de Química/SBQ, 2018.Disponível em: .
APA
Caumo, S. E. da S., Custódio, D., Vicente, A., Alves, C., & Vasconcellos, P. de C. (2018). Concentration of aliphatic and polycyclic aromatic compounds in atmospheric samples collected around a petrochemical site at São Paulo, Brazil. In Resumos. São Paulo: Sociedade Brasileira de Química/SBQ. Recuperado de http://www.sbq.org.br/41ra/anexos/livro-resumos-41ra.pdf
NLM
Caumo SE da S, Custódio D, Vicente A, Alves C, Vasconcellos P de C. Concentration of aliphatic and polycyclic aromatic compounds in atmospheric samples collected around a petrochemical site at São Paulo, Brazil [Internet]. Resumos. 2018 ;Available from: http://www.sbq.org.br/41ra/anexos/livro-resumos-41ra.pdf
Vancouver
Caumo SE da S, Custódio D, Vicente A, Alves C, Vasconcellos P de C. Concentration of aliphatic and polycyclic aromatic compounds in atmospheric samples collected around a petrochemical site at São Paulo, Brazil [Internet]. Resumos. 2018 ;Available from: http://www.sbq.org.br/41ra/anexos/livro-resumos-41ra.pdf
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PONTE, Gino Del; ARCHANJO, Fernando C.; WATANABE, Lilian Y.; DONATE, Paulo Marcos; CAMPOS, Joaquín M. Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions. Arabian Journal of Chemistry, San Diego, v. 11, n. 3, p. 415-425, 2018. Disponível em: < http://dx.doi.org/10.1016/j.arabjc.2016.11.001 > DOI: 10.1016/j.arabjc.2016.11.001.
APA
Ponte, G. D., Archanjo, F. C., Watanabe, L. Y., Donate, P. M., & Campos, J. M. (2018). Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions. Arabian Journal of Chemistry, 11( 3), 415-425. doi:10.1016/j.arabjc.2016.11.001
NLM
Ponte GD, Archanjo FC, Watanabe LY, Donate PM, Campos JM. Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions [Internet]. Arabian Journal of Chemistry. 2018 ; 11( 3): 415-425.Available from: http://dx.doi.org/10.1016/j.arabjc.2016.11.001
Vancouver
Ponte GD, Archanjo FC, Watanabe LY, Donate PM, Campos JM. Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions [Internet]. Arabian Journal of Chemistry. 2018 ; 11( 3): 415-425.Available from: http://dx.doi.org/10.1016/j.arabjc.2016.11.001
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ABNT
VIEIRA, Plínio Salmazo; SOUZA, Tatiana de Arruda Campos Brasil; HONORATO, Rodrigo Vargas; et al. Pyrrole-indolinone SU11652 targets the nucleoside diphosphate kinase from Leishmania parasites. Biochemical and Biophysical Research Communications, New York, v. 488, p. 461-465, 2017. Disponível em: < http://dx.doi.org/10.1016/j.bbrc.2017.05.048 > DOI: 10.1016/j.bbrc.2017.05.048.
APA
Vieira, P. S., Souza, T. de A. C. B., Honorato, R. V., Zanphorlin, L. M., Severiano, K. U., Rocco, S. A., et al. (2017). Pyrrole-indolinone SU11652 targets the nucleoside diphosphate kinase from Leishmania parasites. Biochemical and Biophysical Research Communications, 488, 461-465. doi:10.1016/j.bbrc.2017.05.048
NLM
Vieira PS, Souza T de ACB, Honorato RV, Zanphorlin LM, Severiano KU, Rocco SA, Oliveira AHC de, Cordeiro AT, Oliveira PSL, Giuseppe PO de, Murakami MT. Pyrrole-indolinone SU11652 targets the nucleoside diphosphate kinase from Leishmania parasites [Internet]. Biochemical and Biophysical Research Communications. 2017 ; 488 461-465.Available from: http://dx.doi.org/10.1016/j.bbrc.2017.05.048
Vancouver
Vieira PS, Souza T de ACB, Honorato RV, Zanphorlin LM, Severiano KU, Rocco SA, Oliveira AHC de, Cordeiro AT, Oliveira PSL, Giuseppe PO de, Murakami MT. Pyrrole-indolinone SU11652 targets the nucleoside diphosphate kinase from Leishmania parasites [Internet]. Biochemical and Biophysical Research Communications. 2017 ; 488 461-465.Available from: http://dx.doi.org/10.1016/j.bbrc.2017.05.048
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARBOSA, M. I. F.; PARRA, G. G.; CORREA, R. S.; et al. Reactive nitrogen/oxygen species production by nitro/nitrosyl supramolecular ruthenium porphyrin complexes. Journal of Photochemistry and Photobiology A, Amsterdam, v. 338, p. 152-160, 2017. Disponível em: < http://dx.doi.org/10.1016/j.jphotochem.2017.01.028 > DOI: 10.1016/j.jphotochem.2017.01.028.
APA
Barbosa, M. I. F., Parra, G. G., Correa, R. S., Sampaio, R. N., Magno, L. N., Silva, R. C., et al. (2017). Reactive nitrogen/oxygen species production by nitro/nitrosyl supramolecular ruthenium porphyrin complexes. Journal of Photochemistry and Photobiology A, 338, 152-160. doi:10.1016/j.jphotochem.2017.01.028
NLM
Barbosa MIF, Parra GG, Correa RS, Sampaio RN, Magno LN, Silva RC, Doriguetto AC, Ellena J, Barbosa Neto NM, Batista AA, Gonçalves PJ. Reactive nitrogen/oxygen species production by nitro/nitrosyl supramolecular ruthenium porphyrin complexes [Internet]. Journal of Photochemistry and Photobiology A. 2017 ; 338 152-160.Available from: http://dx.doi.org/10.1016/j.jphotochem.2017.01.028
Vancouver
Barbosa MIF, Parra GG, Correa RS, Sampaio RN, Magno LN, Silva RC, Doriguetto AC, Ellena J, Barbosa Neto NM, Batista AA, Gonçalves PJ. Reactive nitrogen/oxygen species production by nitro/nitrosyl supramolecular ruthenium porphyrin complexes [Internet]. Journal of Photochemistry and Photobiology A. 2017 ; 338 152-160.Available from: http://dx.doi.org/10.1016/j.jphotochem.2017.01.028