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Artigo de periodico
Asymmetric construction of substituted pyrrolidines via 1,3-dipolar cycloaddition of azomethine ylides and chiral acrylates derived from biomass (2014)
Llompart, David F.; Sarotti, Ariel M.; Corne, Valeria; Suárez, Alejandra G.; Spanevello, Rolando A.; Echeverría, Gustavo A.; Piro, Oscar E.; Castellano, Eduardo Ernesto
Source: Tetrahedron Letters. Unidade: IFSC
Subjects: BIOMASSA, CRISTALOGRAFIA
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ABNT
LLOMPART, David F. et al. Asymmetric construction of substituted pyrrolidines via 1,3-dipolar cycloaddition of azomethine ylides and chiral acrylates derived from biomass. Tetrahedron Letters, v. 55, n. 15, p. 2394-2397, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2014.02.113. Acesso em: 28 out. 2024.
APA
Llompart, D. F., Sarotti, A. M., Corne, V., Suárez, A. G., Spanevello, R. A., Echeverría, G. A., et al. (2014). Asymmetric construction of substituted pyrrolidines via 1,3-dipolar cycloaddition of azomethine ylides and chiral acrylates derived from biomass. Tetrahedron Letters, 55( 15), 2394-2397. doi:10.1016/j.tetlet.2014.02.113
NLM
Llompart DF, Sarotti AM, Corne V, Suárez AG, Spanevello RA, Echeverría GA, Piro OE, Castellano EE. Asymmetric construction of substituted pyrrolidines via 1,3-dipolar cycloaddition of azomethine ylides and chiral acrylates derived from biomass [Internet]. Tetrahedron Letters. 2014 ; 55( 15): 2394-2397.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2014.02.113
Vancouver
Llompart DF, Sarotti AM, Corne V, Suárez AG, Spanevello RA, Echeverría GA, Piro OE, Castellano EE. Asymmetric construction of substituted pyrrolidines via 1,3-dipolar cycloaddition of azomethine ylides and chiral acrylates derived from biomass [Internet]. Tetrahedron Letters. 2014 ; 55( 15): 2394-2397.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2014.02.113
Artigo de periodico
Novel sesquiterpene lactones from Eremanthus seidelii (2012)
Sousa, João Paulo Barreto; Tomaz, José Carlos; Silva, Cecilia C. P.; Ellena, Javier ; Lopes, Norberto Peporine; Lopes, João Luis Callegari
Source: Tetrahedron Letters. Unidades: FCFRP, IFSC
Subjects: QUÍMICA ORGÂNICA, PLANTAS, COMPOSTOS CÍCLICOS
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ABNT
SOUSA, João Paulo Barreto et al. Novel sesquiterpene lactones from Eremanthus seidelii. Tetrahedron Letters, v. No 2012, n. 47, p. 6339-6342, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.09.007. Acesso em: 28 out. 2024.
APA
Sousa, J. P. B., Tomaz, J. C., Silva, C. C. P., Ellena, J., Lopes, N. P., & Lopes, J. L. C. (2012). Novel sesquiterpene lactones from Eremanthus seidelii. Tetrahedron Letters, No 2012( 47), 6339-6342. doi:10.1016/j.tetlet.2012.09.007
NLM
Sousa JPB, Tomaz JC, Silva CCP, Ellena J, Lopes NP, Lopes JLC. Novel sesquiterpene lactones from Eremanthus seidelii [Internet]. Tetrahedron Letters. 2012 ; No 2012( 47): 6339-6342.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2012.09.007
Vancouver
Sousa JPB, Tomaz JC, Silva CCP, Ellena J, Lopes NP, Lopes JLC. Novel sesquiterpene lactones from Eremanthus seidelii [Internet]. Tetrahedron Letters. 2012 ; No 2012( 47): 6339-6342.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2012.09.007
Artigo de periodico
Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides (2009)
Singh, Fateh Veer; Amaral, Mônica F. Z. J.; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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ABNT
SINGH, Fateh Veer e AMARAL, Mônica F. Z. J. e STEFANI, Hélio Alexandre. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides. Tetrahedron Letters, v. 50, n. 22, p. 2636-2639, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.03.078. Acesso em: 28 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. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
Vancouver
Singh FV, Amaral MFZJ, Stefani HA. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides [Internet]. Tetrahedron Letters. 2009 ; 50( 22): 2636-2639.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
Artigo de periodico
Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides (2009)
Stefani, Hélio Alexandre ; Pena, Jesus Marcelo; Gueogjian, Kemilla; Petragnani, Nicola; Vaz, Boniek Gontijo; Eberlin, Marcos Nogueira
Source: Tetrahedron Letters. Unidades: FCF, IQ
Subjects: SÍNTESE ORGÂNICA, TELÚRIO, PALÁDIO
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ABNT
STEFANI, Hélio Alexandre et al. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, v. 50, n. 40, p. 5589-5595, 2009Tradução . . Acesso em: 28 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. 28 ]
Vancouver
Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 out. 28 ]
Artigo de periodico
Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes (2009)
Weber, Minéia; Singh, Fateh Veer; Vieira, Adriano Siqueira; Stefani, Hélio Alexandre ; Paixão, Márcio Weber
Source: Tetrahedron Letters. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, POTÁSSIO, PALÁDIO
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ABNT
WEBER, Minéia et al. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes. Tetrahedron Letters, v. 50, n. 30, p. 4324-4327, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.04.127. Acesso em: 28 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. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
Vancouver
Weber M, Singh FV, Vieira AS, Stefani HA, Paixão MW. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4324-4327.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
Artigo de periodico
Synthesis of selenium- and tellurium-containing nucleosides derived from uridine (2009)
Braga, Antonio Luiz; Severo Filho, Wolmar A.; Schwab, Ricardo S.; Rodrigues, Oscar Endrigo Dorneles; Dornelles, Luciano; Braga, Hugo C.; Lüdtke, Diogo, Seibert
Source: Tetrahedron Letters. Unidade: FCF
Subjects: NUCLEOSÍDEOS, SELÊNIO (SÍNTESE), TELÚRIO (SÍNTESE)
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ABNT
BRAGA, Antonio Luiz et al. Synthesis of selenium- and tellurium-containing nucleosides derived from uridine. Tetrahedron Letters, v. 50, n. 25, p. 3005-3007, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.03.164. Acesso em: 28 out. 2024.
APA
Braga, A. L., Severo Filho, W. A., Schwab, R. S., Rodrigues, O. E. D., Dornelles, L., Braga, H. C., & Lüdtke, D. (2009). Synthesis of selenium- and tellurium-containing nucleosides derived from uridine. Tetrahedron Letters, 50( 25), 3005-3007. doi:10.1016/j.tetlet.2009.03.164
NLM
Braga AL, Severo Filho WA, Schwab RS, Rodrigues OED, Dornelles L, Braga HC, Lüdtke D. Synthesis of selenium- and tellurium-containing nucleosides derived from uridine [Internet]. Tetrahedron Letters. 2009 ; 50( 25): 3005-3007.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.164
Vancouver
Braga AL, Severo Filho WA, Schwab RS, Rodrigues OED, Dornelles L, Braga HC, Lüdtke D. Synthesis of selenium- and tellurium-containing nucleosides derived from uridine [Internet]. Tetrahedron Letters. 2009 ; 50( 25): 3005-3007.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.164
Artigo de periodico
Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid (2009)
Singh, Fateh Veer; Milagre, Humberto Márcio Santos; Eberlin, Marcos Nogueira; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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ABNT
SINGH, Fateh Veer et al. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid. Tetrahedron Letters, v. 50, n. 20, p. 2312-2316, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.02.164. Acesso em: 28 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. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
Vancouver
Singh FV, Milagre HMS, Eberlin MN, Stefani HA. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid [Internet]. Tetrahedron Letters. 2009 ; 50( 20): 2312-2316.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
Artigo de periodico
Total synthesis of ('+ OU -')-dihydroactinidiolide using selenium-stabilized carbenium ion (2009)
Dabdoub, Miguel Joaquim; Silveira, Claudio C.; Lenardão, Éder João; Guerrero Jr., Palimécio G.; Viana, Luiz Henrique; Kawasoko, Cristiane Y.; Baroni, Adriano C. M.
Source: Tetrahedron Letters. Unidade: FFCLRP
Subjects: SÍNTESE ORGÂNICA, SILÊNCIO
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ABNT
DABDOUB, Miguel Joaquim et al. Total synthesis of ('+ OU -')-dihydroactinidiolide using selenium-stabilized carbenium ion. Tetrahedron Letters, v. 50, n. 40, p. 5569-5571, 2009Tradução . . Acesso em: 28 out. 2024.
APA
Dabdoub, M. J., Silveira, C. C., Lenardão, É. J., Guerrero Jr., P. G., Viana, L. H., Kawasoko, C. Y., & Baroni, A. C. M. (2009). Total synthesis of ('+ OU -')-dihydroactinidiolide using selenium-stabilized carbenium ion. Tetrahedron Letters, 50( 40), 5569-5571.
NLM
Dabdoub MJ, Silveira CC, Lenardão ÉJ, Guerrero Jr. PG, Viana LH, Kawasoko CY, Baroni ACM. Total synthesis of ('+ OU -')-dihydroactinidiolide using selenium-stabilized carbenium ion. Tetrahedron Letters. 2009 ; 50( 40): 5569-5571.[citado 2024 out. 28 ]
Vancouver
Dabdoub MJ, Silveira CC, Lenardão ÉJ, Guerrero Jr. PG, Viana LH, Kawasoko CY, Baroni ACM. Total synthesis of ('+ OU -')-dihydroactinidiolide using selenium-stabilized carbenium ion. Tetrahedron Letters. 2009 ; 50( 40): 5569-5571.[citado 2024 out. 28 ]
Artigo de periodico
Synthesis and two-photon absorption property of novel salen complexes incorporated with two pendant azo dyes (2009)
Zihong, Ye; De Boni, Leonardo ; Neves, Ubaldo Martins; Mendonça, Cleber Renato ; Xiu, R. B.
Source: Tetrahedron Letters. Unidade: IFSC
Subjects: AZO, CORANTES, FOTÔNICA, METAIS
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ABNT
ZIHONG, Ye et al. Synthesis and two-photon absorption property of novel salen complexes incorporated with two pendant azo dyes. Tetrahedron Letters, v. 50, n. 13, p. 1371-1373, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.12.112. Acesso em: 28 out. 2024.
APA
Zihong, Y., De Boni, L., Neves, U. M., Mendonça, C. R., & Xiu, R. B. (2009). Synthesis and two-photon absorption property of novel salen complexes incorporated with two pendant azo dyes. Tetrahedron Letters, 50( 13), 1371-1373. doi:10.1016/j.tetlet.2008.12.112
NLM
Zihong Y, De Boni L, Neves UM, Mendonça CR, Xiu RB. Synthesis and two-photon absorption property of novel salen complexes incorporated with two pendant azo dyes [Internet]. Tetrahedron Letters. 2009 ; 50( 13): 1371-1373.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.12.112
Vancouver
Zihong Y, De Boni L, Neves UM, Mendonça CR, Xiu RB. Synthesis and two-photon absorption property of novel salen complexes incorporated with two pendant azo dyes [Internet]. Tetrahedron Letters. 2009 ; 50( 13): 1371-1373.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.12.112
Artigo de periodico
Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds (2009)
Keppler, Artur Franz; Gariani, Rogério Aparecido; Lopes, Danilo G.; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Subjects: LÍTIO, CALCOGÊNIOS, SÍNTESE ORGÂNICA
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ABNT
KEPPLER, Artur Franz et al. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds. Tetrahedron Letters, v. 50, n. 19, p. 2181-2184, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.02.158. Acesso em: 28 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. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
Vancouver
Keppler AF, Gariani RA, Lopes DG, Comasseto JV. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds [Internet]. Tetrahedron Letters. 2009 ; 50( 19): 2181-2184.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
Artigo de periodico
Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones (2009)
Princival, Jefferson Luiz; Santos, Alcindo Aparecido dos ; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Subjects: COMPOSTOS ORGANOMETÁLICOS, QUÍMICA ORGÂNICA
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ABNT
PRINCIVAL, Jefferson Luiz e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones. Tetrahedron Letters, v. 46, p. 6368-6371, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.08.097. Acesso em: 28 out. 2024.
APA
Princival, J. L., Santos, A. A. dos, & Comasseto, J. V. (2009). Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones. Tetrahedron Letters, 46, 6368-6371. doi:10.1016/j.tetlet.2009.08.097
NLM
Princival JL, Santos AA dos, Comasseto JV. Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones [Internet]. Tetrahedron Letters. 2009 ; 46 6368-6371.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.08.097
Vancouver
Princival JL, Santos AA dos, Comasseto JV. Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones [Internet]. Tetrahedron Letters. 2009 ; 46 6368-6371.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.08.097
Artigo de periodico
First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B) (2009)
Andrade, Leandro Helgueira ; Silva, Alexandre Vieira; Pedrozo, Eliane Correa
Source: Tetrahedron Letters. Unidade: IQ
Subjects: PALÁDIO, CANDIDA
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ABNT
ANDRADE, Leandro Helgueira e SILVA, Alexandre Vieira e PEDROZO, Eliane Correa. First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B). Tetrahedron Letters, v. 50, n. 30, p. 4331-4334, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.05.022. Acesso em: 28 out. 2024.
APA
Andrade, L. H., Silva, A. V., & Pedrozo, E. C. (2009). First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B). Tetrahedron Letters, 50( 30), 4331-4334. doi:10.1016/j.tetlet.2009.05.022
NLM
Andrade LH, Silva AV, Pedrozo EC. First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B) [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4331-4334.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.05.022
Vancouver
Andrade LH, Silva AV, Pedrozo EC. First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B) [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4331-4334.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2009.05.022
Artigo de periodico
An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization (2009)
Silva Jr., Luiz Fernando da; Quintiliano, Samir Augusto Pino
Source: Tetrahedron Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
SILVA JR., Luiz Fernando da e QUINTILIANO, Samir Augusto Pino. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters, v. 50, n. 19, p. 2256-2260, 2009Tradução . . Acesso em: 28 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. 28 ]
Vancouver
Silva Jr. LF da, Quintiliano SAP. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters. 2009 ; 50( 19): 2256-2260.[citado 2024 out. 28 ]
Artigo de periodico
'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters (2008)
Proti, Patrícia Barrientos; Miranda, Maria Terêsa Machini de
Source: Tetrahedron Letters. Unidade: IQ
Subjects: PROTEÍNAS, BIOQUÍMICA, PEPTÍDEOS (SÍNTESE)
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ABNT
PROTI, Patrícia Barrientos e MIRANDA, Maria Terêsa Machini de. 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters, v. 49, n. 24, p. 3853-3857, 2008Tradução . . Acesso em: 28 out. 2024.
APA
Proti, P. B., & Miranda, M. T. M. de. (2008). 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters, 49( 24), 3853-3857.
NLM
Proti PB, Miranda MTM de. 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters. 2008 ;49( 24): 3853-3857.[citado 2024 out. 28 ]
Vancouver
Proti PB, Miranda MTM de. 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters. 2008 ;49( 24): 3853-3857.[citado 2024 out. 28 ]
Artigo de periodico
Tellurium tetrachloride: an improved method of preparation (2008)
Petragnani, Nicola; Mendes, Samuel Rodrigues; Silveira, Claudio da Cruz
Source: Tetrahedron Letters. Unidade: IQ
Subjects: TELÚRIO, REAGENTES ORGÂNICOS
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ABNT
PETRAGNANI, Nicola e MENDES, Samuel Rodrigues e SILVEIRA, Claudio da Cruz. Tellurium tetrachloride: an improved method of preparation. Tetrahedron Letters, v. 49, n. 15, p. 2371-2372, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.02.085. Acesso em: 28 out. 2024.
APA
Petragnani, N., Mendes, S. R., & Silveira, C. da C. (2008). Tellurium tetrachloride: an improved method of preparation. Tetrahedron Letters, 49( 15), 2371-2372. doi:10.1016/j.tetlet.2008.02.085
NLM
Petragnani N, Mendes SR, Silveira C da C. Tellurium tetrachloride: an improved method of preparation [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2371-2372.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.085
Vancouver
Petragnani N, Mendes SR, Silveira C da C. Tellurium tetrachloride: an improved method of preparation [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2371-2372.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.085
Artigo de periodico
Synthesis of the C7-C24 fragment of (-)-Macrolactin F (2008)
Oliveira, Roberta A.; Oliveira, Juliana M.; Rahmeier, L. H. S.; Comasseto, João Valdir; Marino, Joseph P.; Menezes, Paulo Henrique
Source: Tetrahedron Letters. Unidade: IQ
Subjects: REAGENTES ORGÂNICOS, TELÚRIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Roberta A. et al. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters, v. 49, n. 40, p. 5759-5761, 2008Tradução . . Acesso em: 28 out. 2024.
APA
Oliveira, R. A., Oliveira, J. M., Rahmeier, L. H. S., Comasseto, J. V., Marino, J. P., & Menezes, P. H. (2008). Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters, 49( 40), 5759-5761.
NLM
Oliveira RA, Oliveira JM, Rahmeier LHS, Comasseto JV, Marino JP, Menezes PH. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters. 2008 ; 49( 40): 5759-5761.[citado 2024 out. 28 ]
Vancouver
Oliveira RA, Oliveira JM, Rahmeier LHS, Comasseto JV, Marino JP, Menezes PH. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters. 2008 ; 49( 40): 5759-5761.[citado 2024 out. 28 ]
Artigo de periodico
Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts (2008)
Guadagnin, Rafael Carlos; Suganuma, Carlos Andrei; Singh, Fateh Veer; Vieira, Adriano Siqueira; Cella, Rodrigo; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: QUÍMICA FARMACÊUTICA, TELÚRIO, REAÇÕES ORGÂNICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUADAGNIN, Rafael Carlos et al. Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts. Tetrahedron Letters, v. 49, n. 32, p. 4713-4716, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.05.129. Acesso em: 28 out. 2024.
APA
Guadagnin, R. C., Suganuma, C. A., Singh, F. V., Vieira, A. S., Cella, R., & Stefani, H. A. (2008). Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts. Tetrahedron Letters, 49( 32), 4713-4716. doi:10.1016/j.tetlet.2008.05.129
NLM
Guadagnin RC, Suganuma CA, Singh FV, Vieira AS, Cella R, Stefani HA. Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts [Internet]. Tetrahedron Letters. 2008 ; 49( 32): 4713-4716.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.129
Vancouver
Guadagnin RC, Suganuma CA, Singh FV, Vieira AS, Cella R, Stefani HA. Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts [Internet]. Tetrahedron Letters. 2008 ; 49( 32): 4713-4716.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.129
Artigo de periodico
One-step biomimetic conversion of a furanoheliangolide into an eremantholide using Stryker's reagent (2008)
Sass, Daiane Cristina; Heleno, Vladimir Constantino Gomes; Lopes, João Luis Callegari; Constantino, Maurício Gomes
Source: Tetrahedron Letters. Unidades: FCFRP, FFCLRP
Subjects: FÍSICO-QUÍMICA, PRODUTOS NATURAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SASS, Daiane Cristina et al. One-step biomimetic conversion of a furanoheliangolide into an eremantholide using Stryker's reagent. Tetrahedron Letters, v. 49, n. 24, p. 3877-3880, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.04.071. Acesso em: 28 out. 2024.
APA
Sass, D. C., Heleno, V. C. G., Lopes, J. L. C., & Constantino, M. G. (2008). One-step biomimetic conversion of a furanoheliangolide into an eremantholide using Stryker's reagent. Tetrahedron Letters, 49( 24), 3877-3880. doi:10.1016/j.tetlet.2008.04.071
NLM
Sass DC, Heleno VCG, Lopes JLC, Constantino MG. One-step biomimetic conversion of a furanoheliangolide into an eremantholide using Stryker's reagent [Internet]. Tetrahedron Letters. 2008 ; 49( 24): 3877-3880.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.04.071
Vancouver
Sass DC, Heleno VCG, Lopes JLC, Constantino MG. One-step biomimetic conversion of a furanoheliangolide into an eremantholide using Stryker's reagent [Internet]. Tetrahedron Letters. 2008 ; 49( 24): 3877-3880.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.04.071
Artigo de periodico
Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals (2008)
Guerrero Júnior, Palimécio G.; Dabdoub, Miguel Joaquim; Baroni, Adriano C. M.
Source: Tetrahedron Letters. Unidade: FFCLRP
Assunto: REAÇÕES QUÍMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUERRERO JÚNIOR, Palimécio G. e DABDOUB, Miguel Joaquim e BARONI, Adriano C. M. Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals. Tetrahedron Letters, v. 49, n. 24, p. 3872-3876, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.04.072. Acesso em: 28 out. 2024.
APA
Guerrero Júnior, P. G., Dabdoub, M. J., & Baroni, A. C. M. (2008). Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals. Tetrahedron Letters, 49( 24), 3872-3876. doi:10.1016/j.tetlet.2008.04.072
NLM
Guerrero Júnior PG, Dabdoub MJ, Baroni ACM. Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals [Internet]. Tetrahedron Letters. 2008 ; 49( 24): 3872-3876.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.04.072
Vancouver
Guerrero Júnior PG, Dabdoub MJ, Baroni ACM. Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals [Internet]. Tetrahedron Letters. 2008 ; 49( 24): 3872-3876.[citado 2024 out. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2008.04.072
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: 28 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. 28 ] 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. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.031

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