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Artigo de periodico
Biobased spiroimides from itaconic acid and formamides: molecular targets for a novel synthetic application of renewable chemicals (2020)
Hornink, Milene Macedo; Lopes, Alice Uva; Andrade, Leandro Helgueira
Source: Synthesis. Unidade: IQ
Subjects: ÁCIDOS, FOTOQUÍMICA
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ABNT
HORNINK, Milene Macedo; LOPES, Alice Uva; ANDRADE, Leandro Helgueira. Biobased spiroimides from itaconic acid and formamides: molecular targets for a novel synthetic application of renewable chemicals. Synthesis, Stuttgart, 2020. Disponível em: < http://dx.doi.org/10.1055/s-0040-1707318 > DOI: 10.1055/s-0040-1707318.
APA
Hornink, M. M., Lopes, A. U., & Andrade, L. H. (2020). Biobased spiroimides from itaconic acid and formamides: molecular targets for a novel synthetic application of renewable chemicals. Synthesis. doi:10.1055/s-0040-1707318
NLM
Hornink MM, Lopes AU, Andrade LH. Biobased spiroimides from itaconic acid and formamides: molecular targets for a novel synthetic application of renewable chemicals [Internet]. Synthesis. 2020 ;Available from: http://dx.doi.org/10.1055/s-0040-1707318
Vancouver
Hornink MM, Lopes AU, Andrade LH. Biobased spiroimides from itaconic acid and formamides: molecular targets for a novel synthetic application of renewable chemicals [Internet]. Synthesis. 2020 ;Available from: http://dx.doi.org/10.1055/s-0040-1707318
Artigo de periodico
Green one-pot asymmetric synthesis of peptidomimetics via sequential organocatalyzed aziridination and Passerini multicomponent reaction (2020)
Santos, Deborah A.; Paixão, Marcio W.; Corrêa, Arlene G. ; Silva, Allan R.; Ellena, Javier ; Silva, Cecilia C. P.
Source: Synthesis. Unidade: IFSC
Subjects: QUÍMICA VERDE, PLANEJAMENTO DE FÁRMACOS
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SANTOS, Deborah A.; PAIXÃO, Marcio W.; CORRÊA, Arlene G.; et al. Green one-pot asymmetric synthesis of peptidomimetics via sequential organocatalyzed aziridination and Passerini multicomponent reaction. Synthesis, Stuttgart, Georg Thieme Verlag, v. 52, n. 7, p. 1076-1086, 2020. Disponível em: < http://dx.doi.org/10.1055/s-0039-1690774 > DOI: 10.1055/s-0039-1690774.
APA
Santos, D. A., Paixão, M. W., Corrêa, A. G., Silva, A. R., Ellena, J., & Silva, C. C. P. (2020). Green one-pot asymmetric synthesis of peptidomimetics via sequential organocatalyzed aziridination and Passerini multicomponent reaction. Synthesis, 52( 7), 1076-1086. doi:10.1055/s-0039-1690774
NLM
Santos DA, Paixão MW, Corrêa AG, Silva AR, Ellena J, Silva CCP. Green one-pot asymmetric synthesis of peptidomimetics via sequential organocatalyzed aziridination and Passerini multicomponent reaction [Internet]. Synthesis. 2020 ; 52( 7): 1076-1086.Available from: http://dx.doi.org/10.1055/s-0039-1690774
Vancouver
Santos DA, Paixão MW, Corrêa AG, Silva AR, Ellena J, Silva CCP. Green one-pot asymmetric synthesis of peptidomimetics via sequential organocatalyzed aziridination and Passerini multicomponent reaction [Internet]. Synthesis. 2020 ; 52( 7): 1076-1086.Available from: http://dx.doi.org/10.1055/s-0039-1690774
Artigo de periodico
Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes (2019)
Rodrigues, Shirley Muniz Machado; Previdi, Daniel; Baviera, Giovanni Stoppa; Matias, Alexandre A.; Donate, Paulo Marcos
Source: Synthesis. Unidade: FFCLRP
Subjects: COMPOSTOS ORGÂNICOS, NIÓBIO, ALDEÍDOS
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RODRIGUES, Shirley Muniz Machado; PREVIDI, Daniel; BAVIERA, Giovanni Stoppa; MATIAS, Alexandre A.; DONATE, Paulo Marcos. Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes. Synthesis, Stuttgart, v. 51, n. 23, p. 4498-4506, 2019. Disponível em: < https://doi.org/10.1055/s-0037-1610727 > DOI: 10.1055/s-0037-1610727.
APA
Rodrigues, S. M. M., Previdi, D., Baviera, G. S., Matias, A. A., & Donate, P. M. (2019). Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes. Synthesis, 51( 23), 4498-4506. doi:10.1055/s-0037-1610727
NLM
Rodrigues SMM, Previdi D, Baviera GS, Matias AA, Donate PM. Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes [Internet]. Synthesis. 2019 ; 51( 23): 4498-4506.Available from: https://doi.org/10.1055/s-0037-1610727
Vancouver
Rodrigues SMM, Previdi D, Baviera GS, Matias AA, Donate PM. Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes [Internet]. Synthesis. 2019 ; 51( 23): 4498-4506.Available from: https://doi.org/10.1055/s-0037-1610727
Artigo de periodico
Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives (2017)
Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Oliveira, Isadora Maria de; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre
Source: Synthesis. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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SHAMIM, Anwar; VASCONCELOS, Stanley Nunes Siqueira; OLIVEIRA, Isadora Maria de; et al. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, Stuttgart, v. 49, n. 23, p. 5183-5196, 2017. Disponível em: < http://dx.doi.org/10.1055/s-0036-1589090 > DOI: 10.1055/s-0036-1589090.
APA
Shamim, A., Vasconcelos, S. N. S., Oliveira, I. M. de, Reis, J. S. dos, Pimenta, D. C., Zukerman-Schpector, J., & Stefani, H. A. (2017). Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, 49( 23), 5183-5196. doi:10.1055/s-0036-1589090
NLM
Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.Available from: http://dx.doi.org/10.1055/s-0036-1589090
Vancouver
Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.Available from: http://dx.doi.org/10.1055/s-0036-1589090
Artigo de periodico
Short and diastereoselective total synthesis of the polyhydroxylated pyrrolidine LAB-1: a potent α-glycosidase inhibitor (2017)
Silva, Erica C. da; Yamakawa, Nathalia C. Gonçalves; Santos, Alcindo Aparecido dos ; Coelho, Fernando
Source: Synthesis. Unidade: IQ
Subjects: PRODUTOS NATURAIS, INIBIDORES DE ENZIMAS
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SILVA, Erica C. da; YAMAKAWA, Nathalia C. Gonçalves; SANTOS, Alcindo Aparecido dos; COELHO, Fernando. Short and diastereoselective total synthesis of the polyhydroxylated pyrrolidine LAB-1: a potent α-glycosidase inhibitor. Synthesis, Stuttgart, v. 49, p. 4869-4875, 2017. Disponível em: < http://dx.doi.org/10.1055/s-0036-1590799 > DOI: 10.1055/s-0036-1590799.
APA
Silva, E. C. da, Yamakawa, N. C. G., Santos, A. A. dos, & Coelho, F. (2017). Short and diastereoselective total synthesis of the polyhydroxylated pyrrolidine LAB-1: a potent α-glycosidase inhibitor. Synthesis, 49, 4869-4875. doi:10.1055/s-0036-1590799
NLM
Silva EC da, Yamakawa NCG, Santos AA dos, Coelho F. Short and diastereoselective total synthesis of the polyhydroxylated pyrrolidine LAB-1: a potent α-glycosidase inhibitor [Internet]. Synthesis. 2017 ; 49 4869-4875.Available from: http://dx.doi.org/10.1055/s-0036-1590799
Vancouver
Silva EC da, Yamakawa NCG, Santos AA dos, Coelho F. Short and diastereoselective total synthesis of the polyhydroxylated pyrrolidine LAB-1: a potent α-glycosidase inhibitor [Internet]. Synthesis. 2017 ; 49 4869-4875.Available from: http://dx.doi.org/10.1055/s-0036-1590799
Artigo de periodico
Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds (2016)
Bernardim, Barbara; Couch, Erica D.; Hardman-Baldwin, Andrea M; Burtoloso, Antonio Carlos Bender; Mattson, Anitta E
Source: Synthesis. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, UREIA
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BERNARDIM, Barbara; COUCH, Erica D.; HARDMAN-BALDWIN, Andrea M; BURTOLOSO, Antonio Carlos Bender; MATTSON, Anitta E. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds. Synthesis, Stuttgart, v. 48, n. 5, p. 677-686, 2016. Disponível em: < http://dx.doi.org/10.1055/s-0035-1561061 > DOI: 10.1055/s-0035-1561061; Art ID: ss-2015-e0559-fa.
APA
Bernardim, B., Couch, E. D., Hardman-Baldwin, A. M., Burtoloso, A. C. B., & Mattson, A. E. (2016). Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds. Synthesis, 48( 5), 677-686. doi:10.1055/s-0035-1561061; Art ID: ss-2015-e0559-fa
NLM
Bernardim B, Couch ED, Hardman-Baldwin AM, Burtoloso ACB, Mattson AE. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds [Internet]. Synthesis. 2016 ; 48( 5): 677-686.Available from: http://dx.doi.org/10.1055/s-0035-1561061
Vancouver
Bernardim B, Couch ED, Hardman-Baldwin AM, Burtoloso ACB, Mattson AE. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds [Internet]. Synthesis. 2016 ; 48( 5): 677-686.Available from: http://dx.doi.org/10.1055/s-0035-1561061
Artigo de periodico
A versatile approach to noncoded beta-Hydroxy-alpha-amino esters and alpha-amino acids/esters from Morita-Baylis-Hillman adducts (2015)
Ullah, Hamid; Ferreira, André Vargas; Bendassolli, Jose Albertino ; Rodrigues Junior, Manoel Trindade; Formiga, André Luiz Barboza; Coelho, Fernando
Source: Synthesis. Unidade: CENA
Subjects: AMINOÁCIDOS, QUÍMICA ANALÍTICA
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ULLAH, Hamid; FERREIRA, André Vargas; BENDASSOLLI, Jose Albertino; et al. A versatile approach to noncoded beta-Hydroxy-alpha-amino esters and alpha-amino acids/esters from Morita-Baylis-Hillman adducts. Synthesis, Stuttgart, v. 47, n. 1, p. 113-123, 2015.
APA
Ullah, H., Ferreira, A. V., Bendassolli, J. A., Rodrigues Junior, M. T., Formiga, A. L. B., & Coelho, F. (2015). A versatile approach to noncoded beta-Hydroxy-alpha-amino esters and alpha-amino acids/esters from Morita-Baylis-Hillman adducts. Synthesis, 47( 1), 113-123.
NLM
Ullah H, Ferreira AV, Bendassolli JA, Rodrigues Junior MT, Formiga ALB, Coelho F. A versatile approach to noncoded beta-Hydroxy-alpha-amino esters and alpha-amino acids/esters from Morita-Baylis-Hillman adducts. Synthesis. 2015 ; 47( 1): 113-123.
Vancouver
Ullah H, Ferreira AV, Bendassolli JA, Rodrigues Junior MT, Formiga ALB, Coelho F. A versatile approach to noncoded beta-Hydroxy-alpha-amino esters and alpha-amino acids/esters from Morita-Baylis-Hillman adducts. Synthesis. 2015 ; 47( 1): 113-123.
Artigo de periodico
(Chloromethyl) magnesium chloride–lithium chloride: a chemoselective reagent for the synthesis of functionalized aromatic chlorohydrins (2015)
Nishimura, Rodolfo H. V.; Murie, Valter E.; Soldi, Rafael A.; Clososki, Giuliano César
Source: Synthesis. Unidade: FCFRP
Subjects: ALDEÍDOS, CLORETO, COMPOSTOS ORGANOMETÁLICOS, REAGENTES, SÍNTESE ORGÂNICA
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NISHIMURA, Rodolfo H. V.; MURIE, Valter E.; SOLDI, Rafael A.; CLOSOSKI, Giuliano César. (Chloromethyl) magnesium chloride–lithium chloride: a chemoselective reagent for the synthesis of functionalized aromatic chlorohydrins. Synthesis, Stuttgart, v. 47, n. 10, p. 1455-1460, 2015. Disponível em: < http://dx.doi.org/10.1055/s-0034-1380288 > DOI: 10.1055/s-0034-1380288.
APA
Nishimura, R. H. V., Murie, V. E., Soldi, R. A., & Clososki, G. C. (2015). (Chloromethyl) magnesium chloride–lithium chloride: a chemoselective reagent for the synthesis of functionalized aromatic chlorohydrins. Synthesis, 47( 10), 1455-1460. doi:10.1055/s-0034-1380288
NLM
Nishimura RHV, Murie VE, Soldi RA, Clososki GC. (Chloromethyl) magnesium chloride–lithium chloride: a chemoselective reagent for the synthesis of functionalized aromatic chlorohydrins [Internet]. Synthesis. 2015 ; 47( 10): 1455-1460.Available from: http://dx.doi.org/10.1055/s-0034-1380288
Vancouver
Nishimura RHV, Murie VE, Soldi RA, Clososki GC. (Chloromethyl) magnesium chloride–lithium chloride: a chemoselective reagent for the synthesis of functionalized aromatic chlorohydrins [Internet]. Synthesis. 2015 ; 47( 10): 1455-1460.Available from: http://dx.doi.org/10.1055/s-0034-1380288
Artigo de periodico
Andrómaca de Eurípides: el prólogo y la noción de unidad en la Poética de Aristóteles (2015)
Werner, Christian
Source: Synthesis. Unidade: FFLCH
Subjects: LITERATURA GREGA CLÁSSICA, POÉTICA, TRAGÉDIA (LITERATURA)
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WERNER, Christian. Andrómaca de Eurípides: el prólogo y la noción de unidad en la Poética de Aristóteles. Synthesis, Buenos Aires, v. 22, p. [19 ], 2015. Disponível em: < http://www.synthesis.fahce.unlp.edu.ar/article/view/SYNv22a05/6901 >.
APA
Werner, C. (2015). Andrómaca de Eurípides: el prólogo y la noción de unidad en la Poética de Aristóteles. Synthesis, 22, [19 ]. Recuperado de http://www.synthesis.fahce.unlp.edu.ar/article/view/SYNv22a05/6901
NLM
Werner C. Andrómaca de Eurípides: el prólogo y la noción de unidad en la Poética de Aristóteles [Internet]. Synthesis. 2015 ; 22 [19 ].Available from: http://www.synthesis.fahce.unlp.edu.ar/article/view/SYNv22a05/6901
Vancouver
Werner C. Andrómaca de Eurípides: el prólogo y la noción de unidad en la Poética de Aristóteles [Internet]. Synthesis. 2015 ; 22 [19 ].Available from: http://www.synthesis.fahce.unlp.edu.ar/article/view/SYNv22a05/6901
Artigo de periodico
Iodine-catalyzed aza-prins cyclization: metal-free synthesis and antiproliferative activity of hexahydrobenzol[f]isoquinolines (2013)
Figueiredo, Carlos A. M; Reddy, Kishore Kumar Reddy Kachi; Monteiro, Paula A; Ruiz, Ana Lúcia Tasca Góis de; Silva Junior, Luiz Fernando da
Source: Synthesis. Unidade: IQ
Subjects: ALDEÍDOS, ANTINEOPLÁSICOS
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FIGUEIREDO, Carlos A. M; REDDY, Kishore Kumar Reddy Kachi; MONTEIRO, Paula A; RUIZ, Ana Lúcia Tasca Góis de; SILVA JUNIOR, Luiz Fernando da. Iodine-catalyzed aza-prins cyclization: metal-free synthesis and antiproliferative activity of hexahydrobenzol[f]isoquinolines. Synthesis, Stuttgart, v. 45, n. 8, p. 1076-1082, 2013.
APA
Figueiredo, C. A. M., Reddy, K. K. R. K., Monteiro, P. A., Ruiz, A. L. T. G. de, & Silva Junior, L. F. da. (2013). Iodine-catalyzed aza-prins cyclization: metal-free synthesis and antiproliferative activity of hexahydrobenzol[f]isoquinolines. Synthesis, 45( 8), 1076-1082.
NLM
Figueiredo CAM, Reddy KKRK, Monteiro PA, Ruiz ALTG de, Silva Junior LF da. Iodine-catalyzed aza-prins cyclization: metal-free synthesis and antiproliferative activity of hexahydrobenzol[f]isoquinolines. Synthesis. 2013 ; 45( 8): 1076-1082.
Vancouver
Figueiredo CAM, Reddy KKRK, Monteiro PA, Ruiz ALTG de, Silva Junior LF da. Iodine-catalyzed aza-prins cyclization: metal-free synthesis and antiproliferative activity of hexahydrobenzol[f]isoquinolines. Synthesis. 2013 ; 45( 8): 1076-1082.
Artigo de periodico
On aromatic electrophilic substitution promoted by in situ generated thionium ions (2013)
Amici, Rosana Ribeiro; Di Vitta, Cláudio ; Marzorati, Liliana
Source: Synthesis. Unidade: IQ
Subjects: AROMATIZANTES, COMPOSTOS DE ENXOFRE
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AMICI, Rosana Ribeiro; DI VITTA, Cláudio; MARZORATI, Liliana. On aromatic electrophilic substitution promoted by in situ generated thionium ions. Synthesis, Stuttgant, v. 45, n. 6, p. 798-802, 2013. Disponível em: < http://dx.doi.org/10.1055/s-0032-1318167 > DOI: 10.1055/s-0032-1318167.
APA
Amici, R. R., Di Vitta, C., & Marzorati, L. (2013). On aromatic electrophilic substitution promoted by in situ generated thionium ions. Synthesis, 45( 6), 798-802. doi:10.1055/s-0032-1318167
NLM
Amici RR, Di Vitta C, Marzorati L. On aromatic electrophilic substitution promoted by in situ generated thionium ions [Internet]. Synthesis. 2013 ; 45( 6): 798-802.Available from: http://dx.doi.org/10.1055/s-0032-1318167
Vancouver
Amici RR, Di Vitta C, Marzorati L. On aromatic electrophilic substitution promoted by in situ generated thionium ions [Internet]. Synthesis. 2013 ; 45( 6): 798-802.Available from: http://dx.doi.org/10.1055/s-0032-1318167
Artigo de periodico
Synthesis of chromanes and 4H-chromenes: exploring the oxidation of 2H-chromenes and dihydro-1-benzoxepines by hypervalent iodine(III) (2012)
Ahmad, Anees; Silva Junior, Luiz Fernando da
Source: Synthesis. Unidade: IQ
Assunto: SÍNTESE ORGÂNICA
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AHMAD, Anees; SILVA JUNIOR, Luiz Fernando da. Synthesis of chromanes and 4H-chromenes: exploring the oxidation of 2H-chromenes and dihydro-1-benzoxepines by hypervalent iodine(III). Synthesis, Stuttgart, v. 44, n. 23, p. 3671-3677 : + Supllementary materials ( S1-S16), 2012. Disponível em: < http://dx.doi.org/10.1055/s-0032-1317497 > DOI: 10.1055/s-0032-1317497.
APA
Ahmad, A., & Silva Junior, L. F. da. (2012). Synthesis of chromanes and 4H-chromenes: exploring the oxidation of 2H-chromenes and dihydro-1-benzoxepines by hypervalent iodine(III). Synthesis, 44( 23), 3671-3677 : + Supllementary materials ( S1-S16). doi:10.1055/s-0032-1317497
NLM
Ahmad A, Silva Junior LF da. Synthesis of chromanes and 4H-chromenes: exploring the oxidation of 2H-chromenes and dihydro-1-benzoxepines by hypervalent iodine(III) [Internet]. Synthesis. 2012 ; 44( 23): 3671-3677 : + Supllementary materials ( S1-S16).Available from: http://dx.doi.org/10.1055/s-0032-1317497
Vancouver
Ahmad A, Silva Junior LF da. Synthesis of chromanes and 4H-chromenes: exploring the oxidation of 2H-chromenes and dihydro-1-benzoxepines by hypervalent iodine(III) [Internet]. Synthesis. 2012 ; 44( 23): 3671-3677 : + Supllementary materials ( S1-S16).Available from: http://dx.doi.org/10.1055/s-0032-1317497
Artigo de periodico
Breve nota sobre a etimologia de Dioniso (2012)
Macedo, José Marcos Mariani de
Source: Synthesis. Unidade: FFLCH
Subjects: ETIMOLOGIA, DIONISO
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MACEDO, José Marcos Mariani de. Breve nota sobre a etimologia de Dioniso. Synthesis, Buenos Aires, v. 19, p. 29-41, 2012. Disponível em: < http://www.scielo.org.ar/pdf/synth/v19/v19a01.pdf >.
APA
Macedo, J. M. M. de. (2012). Breve nota sobre a etimologia de Dioniso. Synthesis, 19, 29-41. Recuperado de http://www.scielo.org.ar/pdf/synth/v19/v19a01.pdf
NLM
Macedo JMM de. Breve nota sobre a etimologia de Dioniso [Internet]. Synthesis. 2012 ;19 29-41.Available from: http://www.scielo.org.ar/pdf/synth/v19/v19a01.pdf
Vancouver
Macedo JMM de. Breve nota sobre a etimologia de Dioniso [Internet]. Synthesis. 2012 ;19 29-41.Available from: http://www.scielo.org.ar/pdf/synth/v19/v19a01.pdf
Artigo de periodico
An improved procedure for the preparation of [bis(2,2,2-trifluoroethyl) phosphono]acetic acid (2010)
Prado, Viviana da Silva; Burtoloso, Antonio Carlos Bender
Source: Synthesis. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
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ABNT
PRADO, Viviana da Silva; BURTOLOSO, Antonio Carlos Bender. An improved procedure for the preparation of [bis(2,2,2-trifluoroethyl) phosphono]acetic acid. Synthesis, Stuttgart, v. 10, n. 2, p. 361-363, 2010. Disponível em: < https://www.thieme-connect.com/ejournals/toc/synthesis/99201 >.
APA
Prado, V. da S., & Burtoloso, A. C. B. (2010). An improved procedure for the preparation of [bis(2,2,2-trifluoroethyl) phosphono]acetic acid. Synthesis, 10( 2), 361-363. Recuperado de https://www.thieme-connect.com/ejournals/toc/synthesis/99201
NLM
Prado V da S, Burtoloso ACB. An improved procedure for the preparation of [bis(2,2,2-trifluoroethyl) phosphono]acetic acid [Internet]. Synthesis. 2010 ; 10( 2): 361-363.Available from: https://www.thieme-connect.com/ejournals/toc/synthesis/99201
Vancouver
Prado V da S, Burtoloso ACB. An improved procedure for the preparation of [bis(2,2,2-trifluoroethyl) phosphono]acetic acid [Internet]. Synthesis. 2010 ; 10( 2): 361-363.Available from: https://www.thieme-connect.com/ejournals/toc/synthesis/99201
Artigo de periodico
Thallium(III) in organic synthesis (2010)
Silva Jr., Luiz Fernando da; Carneiro, Vânia Maria Teixeira
Source: Synthesis. Unidade: IQ
Subjects: TÁLIO, OXIDAÇÃO
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ABNT
SILVA JR., Luiz Fernando da; CARNEIRO, Vânia Maria Teixeira. Thallium(III) in organic synthesis. Synthesis, Stuttgart, n. 7, p. 1059-1074, 2010. Disponível em: < http://dx.doi.org/10.1055/s-0029-1218669 > DOI: 10.1055/s-0029-1218669.
APA
Silva Jr., L. F. da, & Carneiro, V. M. T. (2010). Thallium(III) in organic synthesis. Synthesis, ( 7), 1059-1074. doi:10.1055/s-0029-1218669
NLM
Silva Jr. LF da, Carneiro VMT. Thallium(III) in organic synthesis [Internet]. Synthesis. 2010 ;( 7): 1059-1074.Available from: http://dx.doi.org/10.1055/s-0029-1218669
Vancouver
Silva Jr. LF da, Carneiro VMT. Thallium(III) in organic synthesis [Internet]. Synthesis. 2010 ;( 7): 1059-1074.Available from: http://dx.doi.org/10.1055/s-0029-1218669
Artigo de periodico
Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes (2009)
Ferraz, Helena Maria Carvalho; Carneiro, Vânia Maria Teixeira; Silva Junior, Luiz Fernando da
Source: Synthesis. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, TÁLIO, NITRATOS, CARBONO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ, Helena Maria Carvalho; CARNEIRO, Vânia Maria Teixeira; SILVA JUNIOR, Luiz Fernando da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes. Synthesis, Stuttgart, n. 3, p. 385-388, 2009. Disponível em: < http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf >.
APA
Ferraz, H. M. C., Carneiro, V. M. T., & Silva Junior, L. F. da. (2009). Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes. Synthesis, ( 3), 385-388. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
NLM
Ferraz HMC, Carneiro VMT, Silva Junior LF da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes [Internet]. Synthesis. 2009 ;( 3): 385-388.Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
Vancouver
Ferraz HMC, Carneiro VMT, Silva Junior LF da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes [Internet]. Synthesis. 2009 ;( 3): 385-388.Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
Artigo de periodico
Simple and efficient access to 3-ethoxycarbonylpyrroles, benzofurans, and naphthofurans (2009)
Pancote, Camila Garcel; Carvalho, Bruno S. de; Luchez, Cibele V; Fernandes, João Paulo dos Santos; Politi, Mário José ; Brandt, Carlos Alberto
Source: Synthesis. Unidade: IQ
Subjects: COMPOSTOS HETEROCÍCLICOS, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PANCOTE, Camila Garcel; CARVALHO, Bruno S. de; LUCHEZ, Cibele V; et al. Simple and efficient access to 3-ethoxycarbonylpyrroles, benzofurans, and naphthofurans. Synthesis, Stuttgart, n. 23, p. 3963-3966, 2009. Disponível em: < https://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0029-1217053.pdf >.
APA
Pancote, C. G., Carvalho, B. S. de, Luchez, C. V., Fernandes, J. P. dos S., Politi, M. J., & Brandt, C. A. (2009). Simple and efficient access to 3-ethoxycarbonylpyrroles, benzofurans, and naphthofurans. Synthesis, ( 23), 3963-3966. Recuperado de https://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0029-1217053.pdf
NLM
Pancote CG, Carvalho BS de, Luchez CV, Fernandes JP dos S, Politi MJ, Brandt CA. Simple and efficient access to 3-ethoxycarbonylpyrroles, benzofurans, and naphthofurans [Internet]. Synthesis. 2009 ;( 23): 3963-3966.Available from: https://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0029-1217053.pdf
Vancouver
Pancote CG, Carvalho BS de, Luchez CV, Fernandes JP dos S, Politi MJ, Brandt CA. Simple and efficient access to 3-ethoxycarbonylpyrroles, benzofurans, and naphthofurans [Internet]. Synthesis. 2009 ;( 23): 3963-3966.Available from: https://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0029-1217053.pdf
Artigo de periodico
Synthesis of polyalkylated indoles using a thallium(III)-mediated ring-contraction reaction (2007)
Silva Junior, Luiz Fernando da; Craveiro, Marcus Vinicius; Gambardella, Maria Teresa do Prado
Source: Synthesis. Unidades: IQ, IQSC
Assunto: QUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA JUNIOR, Luiz Fernando da; CRAVEIRO, Marcus Vinicius; GAMBARDELLA, Maria Teresa do Prado. Synthesis of polyalkylated indoles using a thallium(III)-mediated ring-contraction reaction. Synthesis, Stuttgart, n. 24, p. 3851-3857, 2007. Disponível em: < http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-2007-990907.pdf >.
APA
Silva Junior, L. F. da, Craveiro, M. V., & Gambardella, M. T. do P. (2007). Synthesis of polyalkylated indoles using a thallium(III)-mediated ring-contraction reaction. Synthesis, ( 24), 3851-3857. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-2007-990907.pdf
NLM
Silva Junior LF da, Craveiro MV, Gambardella MT do P. Synthesis of polyalkylated indoles using a thallium(III)-mediated ring-contraction reaction [Internet]. Synthesis. 2007 ;( 24): 3851-3857.Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-2007-990907.pdf
Vancouver
Silva Junior LF da, Craveiro MV, Gambardella MT do P. Synthesis of polyalkylated indoles using a thallium(III)-mediated ring-contraction reaction [Internet]. Synthesis. 2007 ;( 24): 3851-3857.Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-2007-990907.pdf
Artigo de periodico
Rearrangement of homoallylic alcohols with thallium(III): diastereoselective synthesis of Indans bearing a 'beta'-hydroxy ketone moiety (2007)
Silva Junior, Luiz Fernando da; Quintiliano, Samir Augusto Pino; Craveiro, Marcus Vinicius; Vieira, Fabiana Yamasaki Martins; Ferraz, Helena Maria Carvalho
Source: Synthesis. Unidade: IQ
Subjects: TÁLIO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA JUNIOR, Luiz Fernando da; QUINTILIANO, Samir Augusto Pino; CRAVEIRO, Marcus Vinicius; VIEIRA, Fabiana Yamasaki Martins; FERRAZ, Helena Maria Carvalho. Rearrangement of homoallylic alcohols with thallium(III): diastereoselective synthesis of Indans bearing a 'beta'-hydroxy ketone moiety. Synthesis, Stuttgart, n. 3, p. 355-362, 2007.
APA
Silva Junior, L. F. da, Quintiliano, S. A. P., Craveiro, M. V., Vieira, F. Y. M., & Ferraz, H. M. C. (2007). Rearrangement of homoallylic alcohols with thallium(III): diastereoselective synthesis of Indans bearing a 'beta'-hydroxy ketone moiety. Synthesis, ( 3), 355-362.
NLM
Silva Junior LF da, Quintiliano SAP, Craveiro MV, Vieira FYM, Ferraz HMC. Rearrangement of homoallylic alcohols with thallium(III): diastereoselective synthesis of Indans bearing a 'beta'-hydroxy ketone moiety. Synthesis. 2007 ;( 3): 355-362.
Vancouver
Silva Junior LF da, Quintiliano SAP, Craveiro MV, Vieira FYM, Ferraz HMC. Rearrangement of homoallylic alcohols with thallium(III): diastereoselective synthesis of Indans bearing a 'beta'-hydroxy ketone moiety. Synthesis. 2007 ;( 3): 355-362.
Artigo de periodico
Synthetic approaches to naturally occurring ten-membered-ring lactones (2007)
Ferraz, Helena Maria Carvalho; Bombonato, Fernanda Irene; Longo Junior, Luiz Sidney
Source: Synthesis. Unidade: IQ
Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ, Helena Maria Carvalho; BOMBONATO, Fernanda Irene; LONGO JUNIOR, Luiz Sidney. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis, Stuttgart, n. 21, p. 3261-3285, 2007.
APA
Ferraz, H. M. C., Bombonato, F. I., & Longo Junior, L. S. (2007). Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis, ( 21), 3261-3285.
NLM
Ferraz HMC, Bombonato FI, Longo Junior LS. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis. 2007 ;( 21): 3261-3285.
Vancouver
Ferraz HMC, Bombonato FI, Longo Junior LS. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis. 2007 ;( 21): 3261-3285.

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