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ABNT
VASCONCELOS, Stanley N. S et al. Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, v. 75, p. 1865-1959, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2019.02.001. Acesso em: 24 ago. 2024.
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.[citado 2024 ago. 24 ] Available from: https://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.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2019.02.001
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ABNT
REIS, Joel S et al. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, v. 74, p. 6866-6872, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2018.10.019. Acesso em: 24 ago. 2024.
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.[citado 2024 ago. 24 ] Available from: https://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.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2018.10.019
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ABNT
STEFANI, Hélio Alexandre et al. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters. Tetrahedron, v. 70, n. 20, p. 3243-3248, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2013.11.107. Acesso em: 24 ago. 2024.
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.[citado 2024 ago. 24 ] Available from: https://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.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2013.11.107
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ABNT
BRAGA, Hugo de Campos et al. Synthesis of 5'-seleno-xylofuranosides. Tetrahedron, v. 66, n. 19, p. 3441-3446, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2010.03.033. Acesso em: 24 ago. 2024.
APA
Braga, H. de C., Stefani, H. A., Paixão, M. W., Santos, F. W., & Lüdtke, D. (2010). Synthesis of 5'-seleno-xylofuranosides. Tetrahedron, 66( 19), 3441-3446. doi:10.1016/j.tet.2010.03.033
NLM
Braga H de C, Stefani HA, Paixão MW, Santos FW, Lüdtke D. Synthesis of 5'-seleno-xylofuranosides [Internet]. Tetrahedron. 2010 ; 66( 19): 3441-3446.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2010.03.033
Vancouver
Braga H de C, Stefani HA, Paixão MW, Santos FW, Lüdtke D. Synthesis of 5'-seleno-xylofuranosides [Internet]. Tetrahedron. 2010 ; 66( 19): 3441-3446.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2010.03.033
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ABNT
STEFANI, Hélio Alexandre e GUAREZEMINI, Alexandre Sardelli e CELLA, Rodrigo. Homocoupling reactions of alkynes, alkenes and alkyl compounds. Tetrahedron, v. 66, n. 40, p. 7871-7918, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2010.07.001. Acesso em: 24 ago. 2024.
APA
Stefani, H. A., Guarezemini, A. S., & Cella, R. (2010). Homocoupling reactions of alkynes, alkenes and alkyl compounds. Tetrahedron, 66( 40), 7871-7918. doi:10.1016/j.tet.2010.07.001
NLM
Stefani HA, Guarezemini AS, Cella R. Homocoupling reactions of alkynes, alkenes and alkyl compounds [Internet]. Tetrahedron. 2010 ; 66( 40): 7871-7918.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2010.07.001
Vancouver
Stefani HA, Guarezemini AS, Cella R. Homocoupling reactions of alkynes, alkenes and alkyl compounds [Internet]. Tetrahedron. 2010 ; 66( 40): 7871-7918.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2010.07.001
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ABNT
VIEIRA, Adriano Siqueira et al. Highly efficient palladium-catalyzed suzuki-miyaura reactions pf potassium aryltrifluoroborates with 5-iodo-1,3-dioxin-4-ones in water: an approach to 'alfa'-aryl-'beta'-ketoesters. Tetrahedron, v. 66, n. 3, p. 773-779, 2010Tradução . . Disponível em: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THR-4XNF6C9-7-1&_cdi=5289&_user=5674931&_pii=S0040402009017177&_orig=browse&_coverDate=01%2F16%2F2010&_sk=999339996&view=c&wchp=dGLbVzW-zSkzV&md5=41b70f9b9dfa0a27144aa8419d7514bb&ie=/sdarticle.pdf. Acesso em: 24 ago. 2024.
APA
Vieira, A. S., Cunha, R. L. O. R., Klitzke, C. F., Zukerman-Schpector, J., & Stefani, H. A. (2010). Highly efficient palladium-catalyzed suzuki-miyaura reactions pf potassium aryltrifluoroborates with 5-iodo-1,3-dioxin-4-ones in water: an approach to 'alfa'-aryl-'beta'-ketoesters. Tetrahedron, 66( 3), 773-779. Recuperado de http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THR-4XNF6C9-7-1&_cdi=5289&_user=5674931&_pii=S0040402009017177&_orig=browse&_coverDate=01%2F16%2F2010&_sk=999339996&view=c&wchp=dGLbVzW-zSkzV&md5=41b70f9b9dfa0a27144aa8419d7514bb&ie=/sdarticle.pdf
NLM
Vieira AS, Cunha RLOR, Klitzke CF, Zukerman-Schpector J, Stefani HA. Highly efficient palladium-catalyzed suzuki-miyaura reactions pf potassium aryltrifluoroborates with 5-iodo-1,3-dioxin-4-ones in water: an approach to 'alfa'-aryl-'beta'-ketoesters [Internet]. Tetrahedron. 2010 ; 66( 3): 773-779.[citado 2024 ago. 24 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THR-4XNF6C9-7-1&_cdi=5289&_user=5674931&_pii=S0040402009017177&_orig=browse&_coverDate=01%2F16%2F2010&_sk=999339996&view=c&wchp=dGLbVzW-zSkzV&md5=41b70f9b9dfa0a27144aa8419d7514bb&ie=/sdarticle.pdf
Vancouver
Vieira AS, Cunha RLOR, Klitzke CF, Zukerman-Schpector J, Stefani HA. Highly efficient palladium-catalyzed suzuki-miyaura reactions pf potassium aryltrifluoroborates with 5-iodo-1,3-dioxin-4-ones in water: an approach to 'alfa'-aryl-'beta'-ketoesters [Internet]. Tetrahedron. 2010 ; 66( 3): 773-779.[citado 2024 ago. 24 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THR-4XNF6C9-7-1&_cdi=5289&_user=5674931&_pii=S0040402009017177&_orig=browse&_coverDate=01%2F16%2F2010&_sk=999339996&view=c&wchp=dGLbVzW-zSkzV&md5=41b70f9b9dfa0a27144aa8419d7514bb&ie=/sdarticle.pdf
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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: 24 ago. 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 ago. 24 ] 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 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2008.05.085
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ABNT
VIEIRA, Adriano Siqueira et al. Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles. Tetrahedron, v. 64, n. 15, p. 3306-3314, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.02.006. Acesso em: 24 ago. 2024.
APA
Vieira, A. S., Ferreira, F. da P., Fiorante, P. de F., Guadagnin, R. C., & Stefani, H. A. (2008). Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles. Tetrahedron, 64( 15), 3306-3314. doi:10.1016/j.tet.2008.02.006
NLM
Vieira AS, Ferreira F da P, Fiorante P de F, Guadagnin RC, Stefani HA. Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles [Internet]. Tetrahedron. 2008 ;64( 15): 3306-3314.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2008.02.006
Vancouver
Vieira AS, Ferreira F da P, Fiorante P de F, Guadagnin RC, Stefani HA. Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles [Internet]. Tetrahedron. 2008 ;64( 15): 3306-3314.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2008.02.006
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ABNT
STEFANI, Hélio Alexandre e CELLA, Rodrigo e VIEIRA, Adriano Siqueira. Recent advances in organotrifluoroborates chemistry. Tetrahedron, v. 63, n. 18, p. 3623-3658, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2007.01.061. Acesso em: 24 ago. 2024.
APA
Stefani, H. A., Cella, R., & Vieira, A. S. (2007). Recent advances in organotrifluoroborates chemistry. Tetrahedron, 63( 18), 3623-3658. doi:10.1016/j.tet.2007.01.061
NLM
Stefani HA, Cella R, Vieira AS. Recent advances in organotrifluoroborates chemistry [Internet]. Tetrahedron. 2007 ; 63( 18): 3623-3658.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2007.01.061
Vancouver
Stefani HA, Cella R, Vieira AS. Recent advances in organotrifluoroborates chemistry [Internet]. Tetrahedron. 2007 ; 63( 18): 3623-3658.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2007.01.061
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ABNT
CELLA, Rodrigo e STEFANI, Hélio Alexandre. Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts. Tetrahedron, v. 62, n. 24, p. 5656-5662, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2006.03.090. Acesso em: 24 ago. 2024.
APA
Cella, R., & Stefani, H. A. (2006). Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts. Tetrahedron, 62( 24), 5656-5662. doi:10.1016/j.tet.2006.03.090
NLM
Cella R, Stefani HA. Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts [Internet]. Tetrahedron. 2006 ; 62( 24): 5656-5662.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2006.03.090
Vancouver
Cella R, Stefani HA. Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts [Internet]. Tetrahedron. 2006 ; 62( 24): 5656-5662.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2006.03.090
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ABNT
PETRAGNANI, Nicola e STEFANI, Hélio Alexandre e VALDUGA, Claudete Justina. Recent advances in selenocyclofunctionalization reactions. Tetrahedron, v. 57, n. 8, p. 1411-1448, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(00)01033-4. Acesso em: 24 ago. 2024.
APA
Petragnani, N., Stefani, H. A., & Valduga, C. J. (2001). Recent advances in selenocyclofunctionalization reactions. Tetrahedron, 57( 8), 1411-1448. doi:10.1016/s0040-4020(00)01033-4
NLM
Petragnani N, Stefani HA, Valduga CJ. Recent advances in selenocyclofunctionalization reactions [Internet]. Tetrahedron. 2001 ; 57( 8): 1411-1448.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/s0040-4020(00)01033-4
Vancouver
Petragnani N, Stefani HA, Valduga CJ. Recent advances in selenocyclofunctionalization reactions [Internet]. Tetrahedron. 2001 ; 57( 8): 1411-1448.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/s0040-4020(00)01033-4
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ABNT
COMASSETO, João Valdir et al. Addition of hydrogen helides to acetylenic selenides synthesis of 1-halo-1-selenoalkanes. Tetrahedron, v. 52, n. 29, p. 9687-702, 1996Tradução . . Disponível em: https://doi.org/10.1016/0040-4020(96)00505-4. Acesso em: 24 ago. 2024.
APA
Comasseto, J. V., Menezes, P. H., Stefani, H. A., Zeni, G., & Braga, A. L. (1996). Addition of hydrogen helides to acetylenic selenides synthesis of 1-halo-1-selenoalkanes. Tetrahedron, 52( 29), 9687-702. doi:10.1016/0040-4020(96)00505-4
NLM
Comasseto JV, Menezes PH, Stefani HA, Zeni G, Braga AL. Addition of hydrogen helides to acetylenic selenides synthesis of 1-halo-1-selenoalkanes [Internet]. Tetrahedron. 1996 ;52( 29): 9687-702.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/0040-4020(96)00505-4
Vancouver
Comasseto JV, Menezes PH, Stefani HA, Zeni G, Braga AL. Addition of hydrogen helides to acetylenic selenides synthesis of 1-halo-1-selenoalkanes [Internet]. Tetrahedron. 1996 ;52( 29): 9687-702.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/0040-4020(96)00505-4