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Artigo de periodico-carta/editorial
Identification of fluoroquinolone-resistant extended-spectrum b-lactamase (CTX-M-8)-producing Escherichia coli ST224, ST2179 and ST2308 in buffalo (Bubalus bubalis). [Letter] (2014)
Aizawa, Juliana; Neuwirt, Natalie; Barbato, Leandro; Neves, Patrícia R.; Leigue, Lucianne; Padilha, João; Castro, Antonio Fernando Pestana de; Gregory, Lilian; Lincopan, Nilton
Source: Journal of Antimicrobial Chemotherapy. Unidades: ICB, FMVZ
Subjects: BÚFALOS, ESCHERICHIA COLI, RESISTÊNCIA MICROBIANA ÀS DROGAS
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ABNT
AIZAWA, Juliana et al. Identification of fluoroquinolone-resistant extended-spectrum b-lactamase (CTX-M-8)-producing Escherichia coli ST224, ST2179 and ST2308 in buffalo (Bubalus bubalis). [Letter]. Journal of Antimicrobial Chemotherapy. Oxford: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.1093/jac/dku218. Acesso em: 28 set. 2024. , 2014
APA
Aizawa, J., Neuwirt, N., Barbato, L., Neves, P. R., Leigue, L., Padilha, J., et al. (2014). Identification of fluoroquinolone-resistant extended-spectrum b-lactamase (CTX-M-8)-producing Escherichia coli ST224, ST2179 and ST2308 in buffalo (Bubalus bubalis). [Letter]. Journal of Antimicrobial Chemotherapy. Oxford: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.1093/jac/dku218
NLM
Aizawa J, Neuwirt N, Barbato L, Neves PR, Leigue L, Padilha J, Castro AFP de, Gregory L, Lincopan N. Identification of fluoroquinolone-resistant extended-spectrum b-lactamase (CTX-M-8)-producing Escherichia coli ST224, ST2179 and ST2308 in buffalo (Bubalus bubalis). [Letter] [Internet]. Journal of Antimicrobial Chemotherapy. 2014 ; 69( 10): 2866-2869.[citado 2024 set. 28 ] Available from: https://doi.org/10.1093/jac/dku218
Vancouver
Aizawa J, Neuwirt N, Barbato L, Neves PR, Leigue L, Padilha J, Castro AFP de, Gregory L, Lincopan N. Identification of fluoroquinolone-resistant extended-spectrum b-lactamase (CTX-M-8)-producing Escherichia coli ST224, ST2179 and ST2308 in buffalo (Bubalus bubalis). [Letter] [Internet]. Journal of Antimicrobial Chemotherapy. 2014 ; 69( 10): 2866-2869.[citado 2024 set. 28 ] Available from: https://doi.org/10.1093/jac/dku218
Artigo de periodico
Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides (2009)
Singh, Fateh Veer; Amaral, Mônica F. Z. J.; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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ABNT
SINGH, Fateh Veer e AMARAL, Mônica F. Z. J. e STEFANI, Hélio Alexandre. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides. Tetrahedron Letters, v. 50, n. 22, p. 2636-2639, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.03.078. Acesso em: 28 set. 2024.
APA
Singh, F. V., Amaral, M. F. Z. J., & Stefani, H. A. (2009). Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides. Tetrahedron Letters, 50( 22), 2636-2639. doi:10.1016/j.tetlet.2009.03.078
NLM
Singh FV, Amaral MFZJ, Stefani HA. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides [Internet]. Tetrahedron Letters. 2009 ; 50( 22): 2636-2639.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
Vancouver
Singh FV, Amaral MFZJ, Stefani HA. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides [Internet]. Tetrahedron Letters. 2009 ; 50( 22): 2636-2639.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
Artigo de periodico
Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides (2009)
Stefani, Hélio Alexandre ; Pena, Jesus Marcelo; Gueogjian, Kemilla; Petragnani, Nicola; Vaz, Boniek Gontijo; Eberlin, Marcos Nogueira
Source: Tetrahedron Letters. Unidades: FCF, IQ
Subjects: SÍNTESE ORGÂNICA, TELÚRIO, PALÁDIO
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ABNT
STEFANI, Hélio Alexandre et al. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, v. 50, n. 40, p. 5589-5595, 2009Tradução . . Acesso em: 28 set. 2024.
APA
Stefani, H. A., Pena, J. M., Gueogjian, K., Petragnani, N., Vaz, B. G., & Eberlin, M. N. (2009). Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, 50( 40), 5589-5595.
NLM
Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 set. 28 ]
Vancouver
Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 set. 28 ]
Artigo de periodico
Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes (2009)
Weber, Minéia; Singh, Fateh Veer; Vieira, Adriano Siqueira; Stefani, Hélio Alexandre ; Paixão, Márcio Weber
Source: Tetrahedron Letters. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, POTÁSSIO, PALÁDIO
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ABNT
WEBER, Minéia et al. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes. Tetrahedron Letters, v. 50, n. 30, p. 4324-4327, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.04.127. Acesso em: 28 set. 2024.
APA
Weber, M., Singh, F. V., Vieira, A. S., Stefani, H. A., & Paixão, M. W. (2009). Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes. Tetrahedron Letters, 50( 30), 4324-4327. doi:10.1016/j.tetlet.2009.04.127
NLM
Weber M, Singh FV, Vieira AS, Stefani HA, Paixão MW. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4324-4327.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
Vancouver
Weber M, Singh FV, Vieira AS, Stefani HA, Paixão MW. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4324-4327.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
Artigo de periodico
Design of a modern liposome and bee venom formulation for the traditional VIT-venom immunotherapy (2009)
Silva, Tatiana Cristina; Moura, Sérgio de Paula; Ramos, Henrique R.; Araújo, Pedro Soares de; Costa, Maria Helena Bueno da
Source: Journal of Liposome Research. Unidade: IQ
Subjects: LIPOSSOMOS (ESTABILIZAÇÃO), ABELHAS, VENENOS DE ORIGEM ANIMAL, IMUNOTERAPIA
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ABNT
SILVA, Tatiana Cristina et al. Design of a modern liposome and bee venom formulation for the traditional VIT-venom immunotherapy. Journal of Liposome Research, v. 18, n. 4, p. 353-368, 2009Tradução . . Acesso em: 28 set. 2024.
APA
Silva, T. C., Moura, S. de P., Ramos, H. R., Araújo, P. S. de, & Costa, M. H. B. da. (2009). Design of a modern liposome and bee venom formulation for the traditional VIT-venom immunotherapy. Journal of Liposome Research, 18( 4), 353-368.
NLM
Silva TC, Moura S de P, Ramos HR, Araújo PS de, Costa MHB da. Design of a modern liposome and bee venom formulation for the traditional VIT-venom immunotherapy. Journal of Liposome Research. 2009 ; 18( 4): 353-368.[citado 2024 set. 28 ]
Vancouver
Silva TC, Moura S de P, Ramos HR, Araújo PS de, Costa MHB da. Design of a modern liposome and bee venom formulation for the traditional VIT-venom immunotherapy. Journal of Liposome Research. 2009 ; 18( 4): 353-368.[citado 2024 set. 28 ]
Artigo de periodico
Synthesis of selenium- and tellurium-containing nucleosides derived from uridine (2009)
Braga, Antonio Luiz; Severo Filho, Wolmar A.; Schwab, Ricardo S.; Rodrigues, Oscar Endrigo Dorneles; Dornelles, Luciano; Braga, Hugo C.; Lüdtke, Diogo, Seibert
Source: Tetrahedron Letters. Unidade: FCF
Subjects: NUCLEOSÍDEOS, SELÊNIO (SÍNTESE), TELÚRIO (SÍNTESE)
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ABNT
BRAGA, Antonio Luiz et al. Synthesis of selenium- and tellurium-containing nucleosides derived from uridine. Tetrahedron Letters, v. 50, n. 25, p. 3005-3007, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.03.164. Acesso em: 28 set. 2024.
APA
Braga, A. L., Severo Filho, W. A., Schwab, R. S., Rodrigues, O. E. D., Dornelles, L., Braga, H. C., & Lüdtke, D. (2009). Synthesis of selenium- and tellurium-containing nucleosides derived from uridine. Tetrahedron Letters, 50( 25), 3005-3007. doi:10.1016/j.tetlet.2009.03.164
NLM
Braga AL, Severo Filho WA, Schwab RS, Rodrigues OED, Dornelles L, Braga HC, Lüdtke D. Synthesis of selenium- and tellurium-containing nucleosides derived from uridine [Internet]. Tetrahedron Letters. 2009 ; 50( 25): 3005-3007.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.164
Vancouver
Braga AL, Severo Filho WA, Schwab RS, Rodrigues OED, Dornelles L, Braga HC, Lüdtke D. Synthesis of selenium- and tellurium-containing nucleosides derived from uridine [Internet]. Tetrahedron Letters. 2009 ; 50( 25): 3005-3007.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.164
Artigo de periodico
Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid (2009)
Singh, Fateh Veer; Milagre, Humberto Márcio Santos; Eberlin, Marcos Nogueira; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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ABNT
SINGH, Fateh Veer et al. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid. Tetrahedron Letters, v. 50, n. 20, p. 2312-2316, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.02.164. Acesso em: 28 set. 2024.
APA
Singh, F. V., Milagre, H. M. S., Eberlin, M. N., & Stefani, H. A. (2009). Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid. Tetrahedron Letters, 50( 20), 2312-2316. doi:10.1016/j.tetlet.2009.02.164
NLM
Singh FV, Milagre HMS, Eberlin MN, Stefani HA. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid [Internet]. Tetrahedron Letters. 2009 ; 50( 20): 2312-2316.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
Vancouver
Singh FV, Milagre HMS, Eberlin MN, Stefani HA. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid [Internet]. Tetrahedron Letters. 2009 ; 50( 20): 2312-2316.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
Artigo de periodico
Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent (2009)
Andrade, Leandro Helgueira ; Piovan, Leandro; Pasquini, Mônica D`Arcadia
Source: Tetrahedron Asymmetry. Unidade: IQ
Subjects: ASPERGILLUS, QUÍMICA ORGÂNICA
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ABNT
ANDRADE, Leandro Helgueira e PIOVAN, Leandro e PASQUINI, Mônica D`Arcadia. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, v. 20, n. 13, p. 1521-1525, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.05.033. Acesso em: 28 set. 2024.
APA
Andrade, L. H., Piovan, L., & Pasquini, M. D. `A. (2009). Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, 20( 13), 1521-1525. doi:10.1016/j.tetasy.2009.05.033
NLM
Andrade LH, Piovan L, Pasquini MD`A. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent [Internet]. Tetrahedron Asymmetry. 2009 ; 20( 13): 1521-1525.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
Vancouver
Andrade LH, Piovan L, Pasquini MD`A. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent [Internet]. Tetrahedron Asymmetry. 2009 ; 20( 13): 1521-1525.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
Artigo de periodico
Influence of urea, isopropanol, and propylene glycol on rutin in vitro release from cosmetic semisolid systems estimated by factorial design (2009)
Baby, André Rolim ; Haroutiounian Filho, Carlos Alberto; Sarruf, Fernanda Daud; Pinto, Claudinéia Aparecida Sales de Oliveira ; Kaneko, Telma Mary ; Velasco, Maria Valéria Robles
Source: Drug Development and Industrial Pharmacy. Unidade: FCF
Subjects: COSMETOLOGIA, UREIA, FLAVONÓIDES
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ABNT
BABY, André Rolim et al. Influence of urea, isopropanol, and propylene glycol on rutin in vitro release from cosmetic semisolid systems estimated by factorial design. Drug Development and Industrial Pharmacy, v. 35, n. 3, p. 272-282, 2009Tradução . . Disponível em: http://pdfserve.informaworld.com/276727_731408342_903083640.pdf. Acesso em: 28 set. 2024.
APA
Baby, A. R., Haroutiounian Filho, C. A., Sarruf, F. D., Pinto, C. A. S. de O., Kaneko, T. M., & Velasco, M. V. R. (2009). Influence of urea, isopropanol, and propylene glycol on rutin in vitro release from cosmetic semisolid systems estimated by factorial design. Drug Development and Industrial Pharmacy, 35( 3), 272-282. Recuperado de http://pdfserve.informaworld.com/276727_731408342_903083640.pdf
NLM
Baby AR, Haroutiounian Filho CA, Sarruf FD, Pinto CAS de O, Kaneko TM, Velasco MVR. Influence of urea, isopropanol, and propylene glycol on rutin in vitro release from cosmetic semisolid systems estimated by factorial design [Internet]. Drug Development and Industrial Pharmacy. 2009 ; 35( 3): 272-282.[citado 2024 set. 28 ] Available from: http://pdfserve.informaworld.com/276727_731408342_903083640.pdf
Vancouver
Baby AR, Haroutiounian Filho CA, Sarruf FD, Pinto CAS de O, Kaneko TM, Velasco MVR. Influence of urea, isopropanol, and propylene glycol on rutin in vitro release from cosmetic semisolid systems estimated by factorial design [Internet]. Drug Development and Industrial Pharmacy. 2009 ; 35( 3): 272-282.[citado 2024 set. 28 ] Available from: http://pdfserve.informaworld.com/276727_731408342_903083640.pdf
Artigo de periodico
Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds (2009)
Keppler, Artur Franz; Gariani, Rogério Aparecido; Lopes, Danilo G.; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Subjects: LÍTIO, CALCOGÊNIOS, SÍNTESE ORGÂNICA
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ABNT
KEPPLER, Artur Franz et al. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds. Tetrahedron Letters, v. 50, n. 19, p. 2181-2184, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.02.158. Acesso em: 28 set. 2024.
APA
Keppler, A. F., Gariani, R. A., Lopes, D. G., & Comasseto, J. V. (2009). Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds. Tetrahedron Letters, 50( 19), 2181-2184. doi:10.1016/j.tetlet.2009.02.158
NLM
Keppler AF, Gariani RA, Lopes DG, Comasseto JV. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds [Internet]. Tetrahedron Letters. 2009 ; 50( 19): 2181-2184.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
Vancouver
Keppler AF, Gariani RA, Lopes DG, Comasseto JV. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds [Internet]. Tetrahedron Letters. 2009 ; 50( 19): 2181-2184.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
Artigo de periodico
First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B) (2009)
Andrade, Leandro Helgueira ; Silva, Alexandre Vieira; Pedrozo, Eliane Correa
Source: Tetrahedron Letters. Unidade: IQ
Subjects: PALÁDIO, CANDIDA
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ABNT
ANDRADE, Leandro Helgueira e SILVA, Alexandre Vieira e PEDROZO, Eliane Correa. First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B). Tetrahedron Letters, v. 50, n. 30, p. 4331-4334, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.05.022. Acesso em: 28 set. 2024.
APA
Andrade, L. H., Silva, A. V., & Pedrozo, E. C. (2009). First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B). Tetrahedron Letters, 50( 30), 4331-4334. doi:10.1016/j.tetlet.2009.05.022
NLM
Andrade LH, Silva AV, Pedrozo EC. First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B) [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4331-4334.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.05.022
Vancouver
Andrade LH, Silva AV, Pedrozo EC. First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B) [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4331-4334.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.05.022
Artigo de periodico
An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization (2009)
Silva Jr., Luiz Fernando da; Quintiliano, Samir Augusto Pino
Source: Tetrahedron Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
SILVA JR., Luiz Fernando da e QUINTILIANO, Samir Augusto Pino. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters, v. 50, n. 19, p. 2256-2260, 2009Tradução . . Acesso em: 28 set. 2024.
APA
Silva Jr., L. F. da, & Quintiliano, S. A. P. (2009). An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters, 50( 19), 2256-2260.
NLM
Silva Jr. LF da, Quintiliano SAP. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters. 2009 ; 50( 19): 2256-2260.[citado 2024 set. 28 ]
Vancouver
Silva Jr. LF da, Quintiliano SAP. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters. 2009 ; 50( 19): 2256-2260.[citado 2024 set. 28 ]
Artigo de periodico
Alpha-tocopherol supplementation decreases electronegative low-density lipoprotein concentration [LDL(-)] in haemodialysis patients (2009)
Mafra, Denise; Santos, Felipe Rizzetto; Lobo, Julie Calixto; Grosso, Daniela de Mattos; Barreira, André Luis; Velarde, Luis Guillermo Coca; Abdalla, Dulcinéia Saes Parra ; Leite Jr., Maurilo
Source: Nephrology Dialysis Transplantation. Unidade: FCF
Subjects: LIPOPROTEÍNAS LDL, HEMODIÁLISE, SUPLEMENTAÇÃO ALIMENTAR
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ABNT
MAFRA, Denise et al. Alpha-tocopherol supplementation decreases electronegative low-density lipoprotein concentration [LDL(-)] in haemodialysis patients. Nephrology Dialysis Transplantation, v. 24, n. 5, p. 1587-1592, 2009Tradução . . Disponível em: https://doi.org/10.1093/ndt/gfn760. Acesso em: 28 set. 2024.
APA
Mafra, D., Santos, F. R., Lobo, J. C., Grosso, D. de M., Barreira, A. L., Velarde, L. G. C., et al. (2009). Alpha-tocopherol supplementation decreases electronegative low-density lipoprotein concentration [LDL(-)] in haemodialysis patients. Nephrology Dialysis Transplantation, 24( 5), 1587-1592. doi:10.1093/ndt/gfn760
NLM
Mafra D, Santos FR, Lobo JC, Grosso D de M, Barreira AL, Velarde LGC, Abdalla DSP, Leite Jr. M. Alpha-tocopherol supplementation decreases electronegative low-density lipoprotein concentration [LDL(-)] in haemodialysis patients [Internet]. Nephrology Dialysis Transplantation. 2009 ; 24( 5): 1587-1592.[citado 2024 set. 28 ] Available from: https://doi.org/10.1093/ndt/gfn760
Vancouver
Mafra D, Santos FR, Lobo JC, Grosso D de M, Barreira AL, Velarde LGC, Abdalla DSP, Leite Jr. M. Alpha-tocopherol supplementation decreases electronegative low-density lipoprotein concentration [LDL(-)] in haemodialysis patients [Internet]. Nephrology Dialysis Transplantation. 2009 ; 24( 5): 1587-1592.[citado 2024 set. 28 ] Available from: https://doi.org/10.1093/ndt/gfn760
Artigo de periodico
Ultrasound in heterocycles chemistry (2009)
Cella, Rodrigo; Stefani, Hélio Alexandre
Source: Tetrahedron. Unidade: FCF
Subjects: ULTRASSONOGRAFIA, SÍNTESE ORGÂNICA
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ABNT
CELLA, Rodrigo e STEFANI, Hélio Alexandre. Ultrasound in heterocycles chemistry. Tetrahedron, v. 65, n. 13, p. 2619-2641, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.12.027. Acesso em: 28 set. 2024.
APA
Cella, R., & Stefani, H. A. (2009). Ultrasound in heterocycles chemistry. Tetrahedron, 65( 13), 2619-2641. doi:10.1016/j.tet.2008.12.027
NLM
Cella R, Stefani HA. Ultrasound in heterocycles chemistry [Internet]. Tetrahedron. 2009 ; 65( 13): 2619-2641.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tet.2008.12.027
Vancouver
Cella R, Stefani HA. Ultrasound in heterocycles chemistry [Internet]. Tetrahedron. 2009 ; 65( 13): 2619-2641.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tet.2008.12.027
Artigo de periodico
'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters (2008)
Proti, Patrícia Barrientos; Miranda, Maria Terêsa Machini de
Source: Tetrahedron Letters. Unidade: IQ
Subjects: PROTEÍNAS, BIOQUÍMICA, PEPTÍDEOS (SÍNTESE)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PROTI, Patrícia Barrientos e MIRANDA, Maria Terêsa Machini de. 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters, v. 49, n. 24, p. 3853-3857, 2008Tradução . . Acesso em: 28 set. 2024.
APA
Proti, P. B., & Miranda, M. T. M. de. (2008). 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters, 49( 24), 3853-3857.
NLM
Proti PB, Miranda MTM de. 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters. 2008 ;49( 24): 3853-3857.[citado 2024 set. 28 ]
Vancouver
Proti PB, Miranda MTM de. 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters. 2008 ;49( 24): 3853-3857.[citado 2024 set. 28 ]
Artigo de periodico
Tellurium tetrachloride: an improved method of preparation (2008)
Petragnani, Nicola; Mendes, Samuel Rodrigues; Silveira, Claudio da Cruz
Source: Tetrahedron Letters. Unidade: IQ
Subjects: TELÚRIO, REAGENTES ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PETRAGNANI, Nicola e MENDES, Samuel Rodrigues e SILVEIRA, Claudio da Cruz. Tellurium tetrachloride: an improved method of preparation. Tetrahedron Letters, v. 49, n. 15, p. 2371-2372, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.02.085. Acesso em: 28 set. 2024.
APA
Petragnani, N., Mendes, S. R., & Silveira, C. da C. (2008). Tellurium tetrachloride: an improved method of preparation. Tetrahedron Letters, 49( 15), 2371-2372. doi:10.1016/j.tetlet.2008.02.085
NLM
Petragnani N, Mendes SR, Silveira C da C. Tellurium tetrachloride: an improved method of preparation [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2371-2372.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.085
Vancouver
Petragnani N, Mendes SR, Silveira C da C. Tellurium tetrachloride: an improved method of preparation [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2371-2372.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.085
Artigo de periodico
Synthesis of the C7-C24 fragment of (-)-Macrolactin F (2008)
Oliveira, Roberta A.; Oliveira, Juliana M.; Rahmeier, L. H. S.; Comasseto, João Valdir; Marino, Joseph P.; Menezes, Paulo Henrique
Source: Tetrahedron Letters. Unidade: IQ
Subjects: REAGENTES ORGÂNICOS, TELÚRIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Roberta A. et al. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters, v. 49, n. 40, p. 5759-5761, 2008Tradução . . Acesso em: 28 set. 2024.
APA
Oliveira, R. A., Oliveira, J. M., Rahmeier, L. H. S., Comasseto, J. V., Marino, J. P., & Menezes, P. H. (2008). Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters, 49( 40), 5759-5761.
NLM
Oliveira RA, Oliveira JM, Rahmeier LHS, Comasseto JV, Marino JP, Menezes PH. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters. 2008 ; 49( 40): 5759-5761.[citado 2024 set. 28 ]
Vancouver
Oliveira RA, Oliveira JM, Rahmeier LHS, Comasseto JV, Marino JP, Menezes PH. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters. 2008 ; 49( 40): 5759-5761.[citado 2024 set. 28 ]
Artigo de periodico
Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts (2008)
Guadagnin, Rafael Carlos; Suganuma, Carlos Andrei; Singh, Fateh Veer; Vieira, Adriano Siqueira; Cella, Rodrigo; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: QUÍMICA FARMACÊUTICA, TELÚRIO, REAÇÕES ORGÂNICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUADAGNIN, Rafael Carlos et al. Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts. Tetrahedron Letters, v. 49, n. 32, p. 4713-4716, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.05.129. Acesso em: 28 set. 2024.
APA
Guadagnin, R. C., Suganuma, C. A., Singh, F. V., Vieira, A. S., Cella, R., & Stefani, H. A. (2008). Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts. Tetrahedron Letters, 49( 32), 4713-4716. doi:10.1016/j.tetlet.2008.05.129
NLM
Guadagnin RC, Suganuma CA, Singh FV, Vieira AS, Cella R, Stefani HA. Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts [Internet]. Tetrahedron Letters. 2008 ; 49( 32): 4713-4716.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.129
Vancouver
Guadagnin RC, Suganuma CA, Singh FV, Vieira AS, Cella R, Stefani HA. Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts [Internet]. Tetrahedron Letters. 2008 ; 49( 32): 4713-4716.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.129
Artigo de periodico
Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions (2008)
Vieira, Adriano Siqueira; Fiorante, Pedro de Freitas; Zukerman-Schpector, Júlio; Alves, Diego; Botteselle, Giancarlo Di Vaccari; Stefani, Hélio Alexandre
Source: Tetrahedron. Unidade: FCF
Subjects: POTÁSSIO (SÍNTESE), SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIEIRA, Adriano Siqueira et al. Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions. Tetrahedron, v. 64, n. 30-31, p. 7234-7241, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.05.085. Acesso em: 28 set. 2024.
APA
Vieira, A. S., Fiorante, P. de F., Zukerman-Schpector, J., Alves, D., Botteselle, G. D. V., & Stefani, H. A. (2008). Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions. Tetrahedron, 64( 30-31), 7234-7241. doi:10.1016/j.tet.2008.05.085
NLM
Vieira AS, Fiorante P de F, Zukerman-Schpector J, Alves D, Botteselle GDV, Stefani HA. Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions [Internet]. Tetrahedron. 2008 ; 64( 30-31): 7234-7241.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tet.2008.05.085
Vancouver
Vieira AS, Fiorante P de F, Zukerman-Schpector J, Alves D, Botteselle GDV, Stefani HA. Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions [Internet]. Tetrahedron. 2008 ; 64( 30-31): 7234-7241.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tet.2008.05.085
Artigo de periodico
First chemoenzymatic synthesis of organoselenium amines and amides (2008)
Andrade, Leandro Helgueira ; Silva, Alexandre Vieira
Source: Tetrahedron - Asymmetry. Unidade: IQ
Subjects: AMINAS (COMPOSTOS ORGÂNICOS), REAGENTES ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANDRADE, Leandro Helgueira e SILVA, Alexandre Vieira. First chemoenzymatic synthesis of organoselenium amines and amides. Tetrahedron - Asymmetry, v. 19, n. 10, p. 1175-1181, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2008.04.026. Acesso em: 28 set. 2024.
APA
Andrade, L. H., & Silva, A. V. (2008). First chemoenzymatic synthesis of organoselenium amines and amides. Tetrahedron - Asymmetry, 19( 10), 1175-1181. doi:10.1016/j.tetasy.2008.04.026
NLM
Andrade LH, Silva AV. First chemoenzymatic synthesis of organoselenium amines and amides [Internet]. Tetrahedron - Asymmetry. 2008 ;19( 10): 1175-1181.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetasy.2008.04.026
Vancouver
Andrade LH, Silva AV. First chemoenzymatic synthesis of organoselenium amines and amides [Internet]. Tetrahedron - Asymmetry. 2008 ;19( 10): 1175-1181.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.tetasy.2008.04.026

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