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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: 02 out. 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 out. 02 ] 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 out. 02 ] 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: 02 out. 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 out. 02 ]
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 out. 02 ]
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: 02 out. 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 out. 02 ] 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 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
Artigo de periodico
The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction (2009)
Silva, Márcio S.; Santos, Alcindo Aparecido dos ; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
SILVA, Márcio S. e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters, v. 50, n. 47, p. 6498-6501, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.09.023. Acesso em: 02 out. 2024.
APA
Silva, M. S., Santos, A. A. dos, & Comasseto, J. V. (2009). The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters, 50( 47), 6498-6501. doi:10.1016/j.tetlet.2009.09.023
NLM
Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2009.09.023
Vancouver
Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2009.09.023
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: 02 out. 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 out. 02 ] 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 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
Artigo de periodico
The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2 (2009)
Silva, Márcio S; Santos, Alcindo Aparecido dos ; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Assunto: SÍNTESE ORGÂNICA
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ABNT
SILVA, Márcio S e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2. Tetrahedron Letters, v. 50, n. 47, p. 6498-6501, 2009Tradução . . Disponível em: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-4X66S22-3-1W&_cdi=5290&_user=5674931&_pii=S004040390901733X&_orig=browse&_coverDate=11%2F25%2F2009&_sk=999499952&view=c&wchp=dGLbVlb-zSkzV&md5=ce757759c979f22fc8e2bca9b6dd0800&ie=/sdarticle.pdf. Acesso em: 02 out. 2024.
APA
Silva, M. S., Santos, A. A. dos, & Comasseto, J. V. (2009). The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2. Tetrahedron Letters, 50( 47), 6498-6501. Recuperado de http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-4X66S22-3-1W&_cdi=5290&_user=5674931&_pii=S004040390901733X&_orig=browse&_coverDate=11%2F25%2F2009&_sk=999499952&view=c&wchp=dGLbVlb-zSkzV&md5=ce757759c979f22fc8e2bca9b6dd0800&ie=/sdarticle.pdf
NLM
Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2 [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2024 out. 02 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-4X66S22-3-1W&_cdi=5290&_user=5674931&_pii=S004040390901733X&_orig=browse&_coverDate=11%2F25%2F2009&_sk=999499952&view=c&wchp=dGLbVlb-zSkzV&md5=ce757759c979f22fc8e2bca9b6dd0800&ie=/sdarticle.pdf
Vancouver
Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2 [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2024 out. 02 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-4X66S22-3-1W&_cdi=5290&_user=5674931&_pii=S004040390901733X&_orig=browse&_coverDate=11%2F25%2F2009&_sk=999499952&view=c&wchp=dGLbVlb-zSkzV&md5=ce757759c979f22fc8e2bca9b6dd0800&ie=/sdarticle.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: 02 out. 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 out. 02 ] 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 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
Artigo de periodico
Irreversible inhibition of human cathepsins B, L, S and K by hypervalent tellurium compounds (2009)
Cunha, Rodrigo Luiz Oliveira Rodrigues; Gouvêa, Iuri E; Feitosa, Geovana Prado Vaz; Alves, Márcio Fernando Madureira; Brömme, Dieter; Comasseto, João Valdir; Tersariol, Ivarne Luis dos Santos; Juliano, Luiz
Source: Biological Chemistry. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, TELÚRIO
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ABNT
CUNHA, Rodrigo Luiz Oliveira Rodrigues et al. Irreversible inhibition of human cathepsins B, L, S and K by hypervalent tellurium compounds. Biological Chemistry, v. 390, n. 11, p. 1205-1212, 2009Tradução . . Disponível em: https://doi.org/10.1515/bc.2009.125. Acesso em: 02 out. 2024.
APA
Cunha, R. L. O. R., Gouvêa, I. E., Feitosa, G. P. V., Alves, M. F. M., Brömme, D., Comasseto, J. V., et al. (2009). Irreversible inhibition of human cathepsins B, L, S and K by hypervalent tellurium compounds. Biological Chemistry, 390( 11), 1205-1212. doi:10.1515/bc.2009.125
NLM
Cunha RLOR, Gouvêa IE, Feitosa GPV, Alves MFM, Brömme D, Comasseto JV, Tersariol IL dos S, Juliano L. Irreversible inhibition of human cathepsins B, L, S and K by hypervalent tellurium compounds [Internet]. Biological Chemistry. 2009 ; 390( 11): 1205-1212.[citado 2024 out. 02 ] Available from: https://doi.org/10.1515/bc.2009.125
Vancouver
Cunha RLOR, Gouvêa IE, Feitosa GPV, Alves MFM, Brömme D, Comasseto JV, Tersariol IL dos S, Juliano L. Irreversible inhibition of human cathepsins B, L, S and K by hypervalent tellurium compounds [Internet]. Biological Chemistry. 2009 ; 390( 11): 1205-1212.[citado 2024 out. 02 ] Available from: https://doi.org/10.1515/bc.2009.125
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: 02 out. 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 out. 02 ]
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 out. 02 ]
Artigo de periodico
A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides (2009)
Princival, Jefferson Luiz; Oliveira, Morilo S. C. de; Santos, Alcindo Aparecido dos ; Comasseto, João Valdir
Source: Tetrahedron: Asymmetry. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, LÍTIO, COMPOSTOS ORGÂNICOS
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ABNT
PRINCIVAL, Jefferson Luiz et al. A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides. Tetrahedron: Asymmetry, v. 20, n. 23, p. 2699-2703, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.10.009. Acesso em: 02 out. 2024.
APA
Princival, J. L., Oliveira, M. S. C. de, Santos, A. A. dos, & Comasseto, J. V. (2009). A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides. Tetrahedron: Asymmetry, 20( 23), 2699-2703. doi:10.1016/j.tetasy.2009.10.009
NLM
Princival JL, Oliveira MSC de, Santos AA dos, Comasseto JV. A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides [Internet]. Tetrahedron: Asymmetry. 2009 ; 20( 23): 2699-2703.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetasy.2009.10.009
Vancouver
Princival JL, Oliveira MSC de, Santos AA dos, Comasseto JV. A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides [Internet]. Tetrahedron: Asymmetry. 2009 ; 20( 23): 2699-2703.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetasy.2009.10.009
Artigo de periodico
Tellurium in organic synthesis: the enantioselective synthesis of the pheromone blend components of Mayetiola destructor, Drosophila mulleri and Contarinia pisi (2009)
Ferrarini, Renan dos Santos; Comasseto, João Valdir; Santos, Alcindo Aparecido dos
Source: Tetrahedron: Asymmetry. Unidade: IQ
Subjects: TELÚRIO, SÍNTESE ORGÂNICA
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ABNT
FERRARINI, Renan dos Santos e COMASSETO, João Valdir e SANTOS, Alcindo Aparecido dos. Tellurium in organic synthesis: the enantioselective synthesis of the pheromone blend components of Mayetiola destructor, Drosophila mulleri and Contarinia pisi. Tetrahedron: Asymmetry, v. 20, n. 17, p. 2043-2047, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.08.003. Acesso em: 02 out. 2024.
APA
Ferrarini, R. dos S., Comasseto, J. V., & Santos, A. A. dos. (2009). Tellurium in organic synthesis: the enantioselective synthesis of the pheromone blend components of Mayetiola destructor, Drosophila mulleri and Contarinia pisi. Tetrahedron: Asymmetry, 20( 17), 2043-2047. doi:10.1016/j.tetasy.2009.08.003
NLM
Ferrarini R dos S, Comasseto JV, Santos AA dos. Tellurium in organic synthesis: the enantioselective synthesis of the pheromone blend components of Mayetiola destructor, Drosophila mulleri and Contarinia pisi [Internet]. Tetrahedron: Asymmetry. 2009 ; 20( 17): 2043-2047.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetasy.2009.08.003
Vancouver
Ferrarini R dos S, Comasseto JV, Santos AA dos. Tellurium in organic synthesis: the enantioselective synthesis of the pheromone blend components of Mayetiola destructor, Drosophila mulleri and Contarinia pisi [Internet]. Tetrahedron: Asymmetry. 2009 ; 20( 17): 2043-2047.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetasy.2009.08.003
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: 02 out. 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 out. 02 ] 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 out. 02 ] Available from: https://doi.org/10.1016/j.tet.2008.12.027
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: 02 out. 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 out. 02 ] 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 out. 02 ] Available from: https://doi.org/10.1016/j.tet.2008.05.085
Artigo de periodico
Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles (2008)
Vieira, Adriano Siqueira; Ferreira, Fernando da Paz; Fiorante, Pedro de Freitas; Guadagnin, Rafael Carlos; Stefani, Hélio Alexandre
Source: Tetrahedron. Unidade: FCF
Subjects: QUÍMICA FARMACÊUTICA, POTÁSSIO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 02 out. 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 out. 02 ] 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 out. 02 ] Available from: https://doi.org/10.1016/j.tet.2008.02.006
Artigo de periodico
Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes (2008)
Cella, Rodrigo; Venturoso, Raphael Costa; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: ALDEÍDOS, SÍNTESE ORGÂNICA, BORO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CELLA, Rodrigo e VENTUROSO, Raphael Costa e STEFANI, Hélio Alexandre. Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes. Tetrahedron Letters, v. 49, n. 1, p. 16-19, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.11.031. Acesso em: 02 out. 2024.
APA
Cella, R., Venturoso, R. C., & Stefani, H. A. (2008). Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes. Tetrahedron Letters, 49( 1), 16-19. doi:10.1016/j.tetlet.2007.11.031
NLM
Cella R, Venturoso RC, Stefani HA. Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes [Internet]. Tetrahedron Letters. 2008 ;49( 1): 16-19.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.031
Vancouver
Cella R, Venturoso RC, Stefani HA. Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes [Internet]. Tetrahedron Letters. 2008 ;49( 1): 16-19.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.031
Artigo de periodico
Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes (2008)
Paixão, Márcio Weber; Weber, Minéia; Braga, Antonio Luiz; Azeredo, Juliano Braun de; Deobald, Anna Maria; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: QUÍMICA FARMACÊUTICA, POTÁSSIO, COBRE, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAIXÃO, Márcio Weber et al. Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes. Tetrahedron Letters, v. 49, n. 15, p. 2366-2370, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.02.083. Acesso em: 02 out. 2024.
APA
Paixão, M. W., Weber, M., Braga, A. L., Azeredo, J. B. de, Deobald, A. M., & Stefani, H. A. (2008). Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes. Tetrahedron Letters, 49( 15), 2366-2370. doi:10.1016/j.tetlet.2008.02.083
NLM
Paixão MW, Weber M, Braga AL, Azeredo JB de, Deobald AM, Stefani HA. Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2366-2370.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.083
Vancouver
Paixão MW, Weber M, Braga AL, Azeredo JB de, Deobald AM, Stefani HA. Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2366-2370.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.083
Artigo de periodico
Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives (2008)
Toledo, Fabiano Travanca; Cunha, Rodrigo Luiz Oliveira Rodrigues; Raminelli, Cristiano; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TOLEDO, Fabiano Travanca et al. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives. Tetrahedron Letters, v. 49, n. 5, p. 873-875, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.11.169. Acesso em: 02 out. 2024.
APA
Toledo, F. T., Cunha, R. L. O. R., Raminelli, C., & Comasseto, J. V. (2008). Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives. Tetrahedron Letters, 49( 5), 873-875. doi:10.1016/j.tetlet.2007.11.169
NLM
Toledo FT, Cunha RLOR, Raminelli C, Comasseto JV. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives [Internet]. Tetrahedron Letters. 2008 ;49( 5): 873-875.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.169
Vancouver
Toledo FT, Cunha RLOR, Raminelli C, Comasseto JV. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives [Internet]. Tetrahedron Letters. 2008 ;49( 5): 873-875.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.169
Artigo de periodico
Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide (2008)
Schwab, Ricardo S.; Galetto, Fábio Z.; Azeredo, Juliano Braun de; Braga, Antonio Luiz; Lüdtke, Diogo Seibert; Paixão, Márcio Weber
Source: Tetrahedron Letters. Unidade: FCF
Subjects: CATÁLISE, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SCHWAB, Ricardo S. et al. Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide. Tetrahedron Letters, v. 49, n. 34, p. 5094-5097, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.06.031. Acesso em: 02 out. 2024.
APA
Schwab, R. S., Galetto, F. Z., Azeredo, J. B. de, Braga, A. L., Lüdtke, D. S., & Paixão, M. W. (2008). Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide. Tetrahedron Letters, 49( 34), 5094-5097. doi:10.1016/j.tetlet.2008.06.031
NLM
Schwab RS, Galetto FZ, Azeredo JB de, Braga AL, Lüdtke DS, Paixão MW. Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide [Internet]. Tetrahedron Letters. 2008 ; 49( 34): 5094-5097.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2008.06.031
Vancouver
Schwab RS, Galetto FZ, Azeredo JB de, Braga AL, Lüdtke DS, Paixão MW. Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide [Internet]. Tetrahedron Letters. 2008 ; 49( 34): 5094-5097.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2008.06.031
Artigo de periodico
Tellurium in organic synthesis: synthesis of bioactive butenolides (2007)
Bassora, Bruno Karaski; Da Costa, Carlos Eduardo; Gariani, Rogério Aparecido; Comasseto, João Valdir; Dos Santos, Alcindo Aparecido
Source: Tetrahedron Letters. Unidade: IQ
Subjects: TELÚRIO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BASSORA, Bruno Karaski et al. Tellurium in organic synthesis: synthesis of bioactive butenolides. Tetrahedron Letters, v. 48, n. 8, p. 1485-1487, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.12.063. Acesso em: 02 out. 2024.
APA
Bassora, B. K., Da Costa, C. E., Gariani, R. A., Comasseto, J. V., & Dos Santos, A. A. (2007). Tellurium in organic synthesis: synthesis of bioactive butenolides. Tetrahedron Letters, 48( 8), 1485-1487. doi:10.1016/j.tetlet.2006.12.063
NLM
Bassora BK, Da Costa CE, Gariani RA, Comasseto JV, Dos Santos AA. Tellurium in organic synthesis: synthesis of bioactive butenolides [Internet]. Tetrahedron Letters. 2007 ; 48( 8): 1485-1487.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2006.12.063
Vancouver
Bassora BK, Da Costa CE, Gariani RA, Comasseto JV, Dos Santos AA. Tellurium in organic synthesis: synthesis of bioactive butenolides [Internet]. Tetrahedron Letters. 2007 ; 48( 8): 1485-1487.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2006.12.063
Artigo de periodico
Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 (2007)
Omori, Álvaro Takeo; Assis, Leonardo Fernandes; Andrade, Leandro Helgueira ; Comasseto, João Valdir; Porto, Andre Luiz Meleiro
Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC
Subjects: CANDIDA, SÍNTESE ORGÂNICA, ASPERGILLUS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OMORI, Álvaro Takeo et al. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435. Tetrahedron - Asymmetry, v. 18, n. 9, p. 1048-1053, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2007.04.019. Acesso em: 02 out. 2024.
APA
Omori, Á. T., Assis, L. F., Andrade, L. H., Comasseto, J. V., & Porto, A. L. M. (2007). Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435. Tetrahedron - Asymmetry, 18( 9), 1048-1053. doi:10.1016/j.tetasy.2007.04.019
NLM
Omori ÁT, Assis LF, Andrade LH, Comasseto JV, Porto ALM. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1048-1053.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
Vancouver
Omori ÁT, Assis LF, Andrade LH, Comasseto JV, Porto ALM. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1048-1053.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019

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