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FURNIEL, Lucas Giani; BURTOLOSO, Antonio Carlos Bender. Copper-catalyzed NeH insertion reactions from sulfoxonium ylides. Tetrahedron, Oxford, v. 76, n. 51, p. 131313, 2020. Disponível em: < https://doi.org/10.1016/j.tet.2020.131313 > DOI: 10.1016/j.tet.2020.131313.
APA
Furniel, L. G., & Burtoloso, A. C. B. (2020). Copper-catalyzed NeH insertion reactions from sulfoxonium ylides. Tetrahedron, 76( 51), 131313. doi:10.1016/j.tet.2020.131313
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PERECIM, Givago P.; DEFLON, Victor Marcelo; MARTINS, Gabriel R.; et al. Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry. Tetrahedron, Oxford, v. 76. 131461 July 2020, 2020. Disponível em: < https://doi.org/10.1016/j.tet.2020.131461 > DOI: 10.1016/j.tet.2020.131461.
APA
Perecim, G. P., Deflon, V. M., Martins, G. R., Pinto, L. M. C., Casagrande, G. A., Silva, D. O., & Raminelli, C. (2020). Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry. Tetrahedron, 76. 131461 July 2020. doi:10.1016/j.tet.2020.131461
NLM
Perecim GP, Deflon VM, Martins GR, Pinto LMC, Casagrande GA, Silva DO, Raminelli C. Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry [Internet]. Tetrahedron. 2020 ; 76. 131461 July 2020Available from: https://doi.org/10.1016/j.tet.2020.131461
Vancouver
Perecim GP, Deflon VM, Martins GR, Pinto LMC, Casagrande GA, Silva DO, Raminelli C. Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry [Internet]. Tetrahedron. 2020 ; 76. 131461 July 2020Available from: https://doi.org/10.1016/j.tet.2020.131461
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NISHIMURA, Rodolfo Hideki Vicente; VAZ, Artur de Lara Lima; BOZZINI, Leandro Alves; MURIE, Valter Eduardo; CLOSOSKI, Giuliano Cesar. Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets. Tetrahedron, Oxford, v. 75, n. 4, p. 464-474, 2019. Disponível em: < https://doi.org/10.1016/j.tet.2018.12.018 > DOI: 10.1016/j.tet.2018.12.018.
APA
Nishimura, R. H. V., Vaz, A. de L. L., Bozzini, L. A., Murie, V. E., & Clososki, G. C. (2019). Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets. Tetrahedron, 75( 4), 464-474. doi:10.1016/j.tet.2018.12.018
NLM
Nishimura RHV, Vaz A de LL, Bozzini LA, Murie VE, Clososki GC. Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets [Internet]. Tetrahedron. 2019 ; 75( 4): 464-474.Available from: https://doi.org/10.1016/j.tet.2018.12.018
Vancouver
Nishimura RHV, Vaz A de LL, Bozzini LA, Murie VE, Clososki GC. Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets [Internet]. Tetrahedron. 2019 ; 75( 4): 464-474.Available from: https://doi.org/10.1016/j.tet.2018.12.018
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VASCONCELOS, Stanley N. S; REIS, Joel S; OLIVEIRA, Isadora M. de; BALFOUR, Michael N; STEFANI, Hélio Alexandre. Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, Oxford, v. 75, p. 1865-1959, 2019. Disponível em: < http://dx.doi.org/10.1016/j.tet.2019.02.001 > DOI: 10.1016/j.tet.2019.02.001.
APA
Vasconcelos, S. N. S., Reis, J. S., Oliveira, I. M. de, Balfour, M. N., & Stefani, H. A. (2019). Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, 75, 1865-1959. doi:10.1016/j.tet.2019.02.001
NLM
Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.Available from: http://dx.doi.org/10.1016/j.tet.2019.02.001
Vancouver
Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.Available from: http://dx.doi.org/10.1016/j.tet.2019.02.001
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MARTELLI, Lorena S. R.; VIEIRA, Lucas C. C.; PAIXÃO, Márcio W.; et al. Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity. Tetrahedron, Oxford, v. 75, n. 25, p. 3530-3542, 2019. Disponível em: < http://dx.doi.org/10.1016/j.tet.2019.05.022 > DOI: 10.1016/j.tet.2019.05.022.
APA
Martelli, L. S. R., Vieira, L. C. C., Paixão, M. W., Zukerman-Schpector, J., Souza, J. O., Aguiar, A. C. C., et al. (2019). Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity. Tetrahedron, 75( 25), 3530-3542. doi:10.1016/j.tet.2019.05.022
NLM
Martelli LSR, Vieira LCC, Paixão MW, Zukerman-Schpector J, Souza JO, Aguiar ACC, Oliva G, Guido RVC, Corrêa AG. Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity [Internet]. Tetrahedron. 2019 ; 75( 25): 3530-3542.Available from: http://dx.doi.org/10.1016/j.tet.2019.05.022
Vancouver
Martelli LSR, Vieira LCC, Paixão MW, Zukerman-Schpector J, Souza JO, Aguiar ACC, Oliva G, Guido RVC, Corrêa AG. Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity [Internet]. Tetrahedron. 2019 ; 75( 25): 3530-3542.Available from: http://dx.doi.org/10.1016/j.tet.2019.05.022
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ABNT
REIS, Joel S; FERNANDES, Arthur Bonfá; DÖRR, Barbara Coelho de Freitas; BASTOS, Erick Leite; STEFANI, Hélio Alexandre. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, Oxford, v. 74, p. 6866-6872, 2018. Disponível em: < http://dx.doi.org/10.1016/j.tet.2018.10.019 > DOI: 10.1016/j.tet.2018.10.019.
APA
Reis, J. S., Fernandes, A. B., Dörr, B. C. de F., Bastos, E. L., & Stefani, H. A. (2018). Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, 74, 6866-6872. doi:10.1016/j.tet.2018.10.019
NLM
Reis JS, Fernandes AB, Dörr BC de F, Bastos EL, Stefani HA. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer [Internet]. Tetrahedron. 2018 ; 74 6866-6872.Available from: http://dx.doi.org/10.1016/j.tet.2018.10.019
Vancouver
Reis JS, Fernandes AB, Dörr BC de F, Bastos EL, Stefani HA. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer [Internet]. Tetrahedron. 2018 ; 74 6866-6872.Available from: http://dx.doi.org/10.1016/j.tet.2018.10.019
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ABNT
LIMA, Rafaely Nascimento; PORTO, André Luiz Meleiro. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol. Tetrahedron, Oxford, v. 58, n. 9, p. 825-828, 2017. Disponível em: < http://dx.doi.org/10.1016/j.tetlet.2016.12.062 > DOI: 10.1016/j.tetlet.2016.12.062.
APA
Lima, R. N., & Porto, A. L. M. (2017). Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol. Tetrahedron, 58( 9), 825-828. doi:10.1016/j.tetlet.2016.12.062
NLM
Lima RN, Porto ALM. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol [Internet]. Tetrahedron. 2017 ; 58( 9): 825-828.Available from: http://dx.doi.org/10.1016/j.tetlet.2016.12.062
Vancouver
Lima RN, Porto ALM. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol [Internet]. Tetrahedron. 2017 ; 58( 9): 825-828.Available from: http://dx.doi.org/10.1016/j.tetlet.2016.12.062
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ABNT
DIAS, Rafael Mafra de Paula; MOMO, Patrícia Betoni; BURTOLOSO, Antonio Carlos Bender. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin. Tetrahedron, Oxford, v. 73, n. 26, p. 3720 - 3729, 2017. Disponível em: < http://dx.doi.org/10.1016/j.tet.2017.05.040 > DOI: 10.1016/j.tet.2017.05.040.
APA
Dias, R. M. de P., Momo, P. B., & Burtoloso, A. C. B. (2017). One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin. Tetrahedron, 73( 26), 3720 - 3729. doi:10.1016/j.tet.2017.05.040
NLM
Dias RM de P, Momo PB, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin [Internet]. Tetrahedron. 2017 ; 73( 26): 3720 - 3729.Available from: http://dx.doi.org/10.1016/j.tet.2017.05.040
Vancouver
Dias RM de P, Momo PB, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin [Internet]. Tetrahedron. 2017 ; 73( 26): 3720 - 3729.Available from: http://dx.doi.org/10.1016/j.tet.2017.05.040
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JIMENEZ, David Esteban Quintero; FERREIRA , Irlon Maciel; BIROLLI, Willian Garcia; FONSECA, Luis P.; PORTO, Andre Luiz Meleiro. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, Oxford, v. 72, n. 46, p. 7317-7322, 2016. Disponível em: < http://dx.doi.org/10.1016/j.tet.2016.02.014 > DOI: 10.1016/j.tet.2016.02.014.
APA
Jimenez, D. E. Q., Ferreira , I. M., Birolli, W. G., Fonseca, L. P., & Porto, A. L. M. (2016). Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, 72( 46), 7317-7322. doi:10.1016/j.tet.2016.02.014
NLM
Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.Available from: http://dx.doi.org/10.1016/j.tet.2016.02.014
Vancouver
Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.Available from: http://dx.doi.org/10.1016/j.tet.2016.02.014
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COSTA, Damien; GALVÃO, Adelino M; DI PAOLO, Roberto E; et al. Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation. Tetrahedron, Hoboken, v. 71, n. 20, p. 3157-3162, 2015. Disponível em: < http://dx.doi.org/10.1016/j.tet.2014.06.092 > DOI: 10.1016/j.tet.2014.06.092.
APA
Costa, D., Galvão, A. M., Di Paolo, R. E., Freitas, A. A. de, Lima, J. C., Quina, F. H., & Maçanita, A. L. (2015). Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation. Tetrahedron, 71( 20), 3157-3162. doi:10.1016/j.tet.2014.06.092
NLM
Costa D, Galvão AM, Di Paolo RE, Freitas AA de, Lima JC, Quina FH, Maçanita AL. Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation [Internet]. Tetrahedron. 2015 ; 71( 20): 3157-3162.Available from: http://dx.doi.org/10.1016/j.tet.2014.06.092
Vancouver
Costa D, Galvão AM, Di Paolo RE, Freitas AA de, Lima JC, Quina FH, Maçanita AL. Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation [Internet]. Tetrahedron. 2015 ; 71( 20): 3157-3162.Available from: http://dx.doi.org/10.1016/j.tet.2014.06.092
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SILVA, Alexandre Vieira; LOPEZ SANCHEZ, Almudena; JUNQUEIRA, Helena Couto; et al. Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites. Tetrahedron, Oxford, v. 71, n. 3, p. 457-462, 2015. Disponível em: < http://dx.doi.org/10.1016/j.tet.2014.11.072 > DOI: 10.1016/j.tet.2014.11.072.
APA
Silva, A. V., Lopez Sanchez, A., Junqueira, H. C., Rivas, L., Baptista, M. da S., & Orellana, G. (2015). Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites. Tetrahedron, 71( 3), 457-462. doi:10.1016/j.tet.2014.11.072
NLM
Silva AV, Lopez Sanchez A, Junqueira HC, Rivas L, Baptista M da S, Orellana G. Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites [Internet]. Tetrahedron. 2015 ; 71( 3): 457-462.Available from: http://dx.doi.org/10.1016/j.tet.2014.11.072
Vancouver
Silva AV, Lopez Sanchez A, Junqueira HC, Rivas L, Baptista M da S, Orellana G. Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites [Internet]. Tetrahedron. 2015 ; 71( 3): 457-462.Available from: http://dx.doi.org/10.1016/j.tet.2014.11.072
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ABNT
CAMPO, Vanessa Leiria; IVANOVA, Irina M.; CARVALHO, Ivone; et al. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion. Tetrahedron, Kidlington, v. 71, n. 39, p. 7344–7353, 2015. Disponível em: < http://dx.doi.org/10.1016/j.tet.2015.04.085 > DOI: 10.1016/j.tet.2015.04.085.
APA
Campo, V. L., Ivanova, I. M., Carvalho, I., Lopes, C. D., Carneiro, Z., Saalbach, G., et al. (2015). Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion. Tetrahedron, 71( 39), 7344–7353. doi:10.1016/j.tet.2015.04.085
NLM
Campo VL, Ivanova IM, Carvalho I, Lopes CD, Carneiro Z, Saalbach G, Schenkman S, Silva JS da, Nepogodiev SA, Field RA. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion [Internet]. Tetrahedron. 2015 ; 71( 39): 7344–7353.Available from: http://dx.doi.org/10.1016/j.tet.2015.04.085
Vancouver
Campo VL, Ivanova IM, Carvalho I, Lopes CD, Carneiro Z, Saalbach G, Schenkman S, Silva JS da, Nepogodiev SA, Field RA. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion [Internet]. Tetrahedron. 2015 ; 71( 39): 7344–7353.Available from: http://dx.doi.org/10.1016/j.tet.2015.04.085
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ABNT
SILVA, Fernanda Parra da; ROSSI, Liane Marcia. Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds. Tetrahedron, Oxford, v. 70, n. 20, p. 3314-3318, 2014. Disponível em: < http://dx.doi.org/10.1016/j.tet.2013.10.051 > DOI: 10.1016/j.tet.2013.10.051.
APA
Silva, F. P. da, & Rossi, L. M. (2014). Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds. Tetrahedron, 70( 20), 3314-3318. doi:10.1016/j.tet.2013.10.051
NLM
Silva FP da, Rossi LM. Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds [Internet]. Tetrahedron. 2014 ; 70( 20): 3314-3318.Available from: http://dx.doi.org/10.1016/j.tet.2013.10.051
Vancouver
Silva FP da, Rossi LM. Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds [Internet]. Tetrahedron. 2014 ; 70( 20): 3314-3318.Available from: http://dx.doi.org/10.1016/j.tet.2013.10.051
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ABNT
SANTOS, Alcindo Aparecido dos. Professor Alcindo A. dos Santos (Biography). Tetrahedron[S.l: s.n.], 2014.Disponível em: DOI: 10.1016/j.tet.2014.03.077.
APA
Santos, A. A. dos. (2014). Professor Alcindo A. dos Santos (Biography). Tetrahedron. Oxford. doi:10.1016/j.tet.2014.03.077
NLM
Santos AA dos. Professor Alcindo A. dos Santos (Biography) [Internet]. Tetrahedron. 2014 ; 70 3229.Available from: http://dx.doi.org/10.1016/j.tet.2014.03.077
Vancouver
Santos AA dos. Professor Alcindo A. dos Santos (Biography) [Internet]. Tetrahedron. 2014 ; 70 3229.Available from: http://dx.doi.org/10.1016/j.tet.2014.03.077
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ABNT
DONATONI, Maria C; JUNIOR, Gilmar A. B; OLIVEIRA, Kleber T. de; et al. Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica. Tetrahedron, Oxford, v. 70, n. 20, p. 3231-3238, 2014. Disponível em: < http://dx.doi.org/10.1016/j.tet.2014.02.017 > DOI: 10.1016/j.tet.2014.02.017.
APA
Donatoni, M. C., Junior, G. A. B., Oliveira, K. T. de, Ando, R. A., Brocksom, T. J., & Santos, A. A. dos. (2014). Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica. Tetrahedron, 70( 20), 3231-3238. doi:10.1016/j.tet.2014.02.017
NLM
Donatoni MC, Junior GAB, Oliveira KT de, Ando RA, Brocksom TJ, Santos AA dos. Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica [Internet]. Tetrahedron. 2014 ; 70( 20): 3231-3238.Available from: http://dx.doi.org/10.1016/j.tet.2014.02.017
Vancouver
Donatoni MC, Junior GAB, Oliveira KT de, Ando RA, Brocksom TJ, Santos AA dos. Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica [Internet]. Tetrahedron. 2014 ; 70( 20): 3231-3238.Available from: http://dx.doi.org/10.1016/j.tet.2014.02.017
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ABNT
BERNARDIM, Barbara; BURTOLOSO, Antonio Carlos Bender. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal. Tetrahedron, Oxford, v. 70, p. 3291-3296, 2014. Disponível em: < http://dx.doi.org/10.1016/j.tet.2013.10.059 > DOI: 10.1016/j.tet.2013.10.059.
APA
Bernardim, B., & Burtoloso, A. C. B. (2014). A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal. Tetrahedron, 70, 3291-3296. doi:10.1016/j.tet.2013.10.059
NLM
Bernardim B, Burtoloso ACB. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal [Internet]. Tetrahedron. 2014 ; 70 3291-3296.Available from: http://dx.doi.org/10.1016/j.tet.2013.10.059
Vancouver
Bernardim B, Burtoloso ACB. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal [Internet]. Tetrahedron. 2014 ; 70 3291-3296.Available from: http://dx.doi.org/10.1016/j.tet.2013.10.059
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ABNT
STEFANI, Hélio Alexandre; MANARIN, Flávia; SOUSA, Ariane C.S; SOUZA, Frederico B; FERRAZ, Witor Ribeiro. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters. Tetrahedron, Oxford, v. 70, n. 20, p. 3243-3248, 2014. Disponível em: < http://dx.doi.org/10.1016/j.tet.2013.11.107 > DOI: 10.1016/j.tet.2013.11.107.
APA
Stefani, H. A., Manarin, F., Sousa, A. C. S., Souza, F. B., & Ferraz, W. R. (2014). Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters. Tetrahedron, 70( 20), 3243-3248. doi:10.1016/j.tet.2013.11.107
NLM
Stefani HA, Manarin F, Sousa ACS, Souza FB, Ferraz WR. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters [Internet]. Tetrahedron. 2014 ; 70( 20): 3243-3248.Available from: http://dx.doi.org/10.1016/j.tet.2013.11.107
Vancouver
Stefani HA, Manarin F, Sousa ACS, Souza FB, Ferraz WR. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters [Internet]. Tetrahedron. 2014 ; 70( 20): 3243-3248.Available from: http://dx.doi.org/10.1016/j.tet.2013.11.107
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SANTOS, Alcindo Aparecido dos. Applied organic synthesis in action [Preface]: strategies and process development. Tetrahedron[S.l: s.n.], 2014.Disponível em: DOI: 10.1016/j.tet.2014.02.053.
APA
Santos, A. A. dos. (2014). Applied organic synthesis in action [Preface]: strategies and process development. Tetrahedron. Oxford. doi:10.1016/j.tet.2014.02.053
NLM
Santos AA dos. Applied organic synthesis in action [Preface]: strategies and process development [Internet]. Tetrahedron. 2014 ; 70 3230.Available from: http://dx.doi.org/10.1016/j.tet.2014.02.053
Vancouver
Santos AA dos. Applied organic synthesis in action [Preface]: strategies and process development [Internet]. Tetrahedron. 2014 ; 70 3230.Available from: http://dx.doi.org/10.1016/j.tet.2014.02.053
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ABNT
BRONDANI, Patricia Bulegon; GUILMOTO, Nathalie Mariana Andrade de França; DUDEK, Hanna M; FRAAIJE, Marco W; ANDRADE, Leandro Helgueira. Chemoenzymatic approaches to obtain chiral-centered selenium compounds. Tetrahedron, Oxford, v. 68, n. 51, p. 10431-10436, 2012. Disponível em: < http://dx.doi.org/10.1016/j.tet.2012.09.087 > DOI: 10.1016/j.tet.2012.09.087.
APA
Brondani, P. B., Guilmoto, N. M. A. de F., Dudek, H. M., Fraaije, M. W., & Andrade, L. H. (2012). Chemoenzymatic approaches to obtain chiral-centered selenium compounds. Tetrahedron, 68( 51), 10431-10436. doi:10.1016/j.tet.2012.09.087
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ABNT
SOUSA, Bruno Artur de; KEPPLER, Arthur Franz; GARIANI, Rogério Aparecido; COMASSETO, João Valdir; SANTOS, Alcindo Aparecido dos. Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts. Tetrahedron, Oxford, v. 68, n. 51, p. 10406-10413, 2012. Disponível em: < http://dx.doi.org/10.1016/j.tet.2012.09.027 > DOI: 10.1016/j.tet.2012.09.027.
APA
Sousa, B. A. de, Keppler, A. F., Gariani, R. A., Comasseto, J. V., & Santos, A. A. dos. (2012). Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts. Tetrahedron, 68( 51), 10406-10413. doi:10.1016/j.tet.2012.09.027
NLM
Sousa BA de, Keppler AF, Gariani RA, Comasseto JV, Santos AA dos. Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts [Internet]. Tetrahedron. 2012 ; 68( 51): 10406-10413.Available from: http://dx.doi.org/10.1016/j.tet.2012.09.027
Vancouver
Sousa BA de, Keppler AF, Gariani RA, Comasseto JV, Santos AA dos. Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts [Internet]. Tetrahedron. 2012 ; 68( 51): 10406-10413.Available from: http://dx.doi.org/10.1016/j.tet.2012.09.027