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Artigo de periodico
Palladium-catalyzed C–H alkenylation of quinoxaline N-oxide enabled by a mono-N-protected amino acid (2018)
Franco, Márcia Silvana Freire; Paula, Murilo Helder de; Glowacka, Paulina Cecylia; Fumagalli, Fernando; Clososki, Giuliano Cesar; Emery, Flavio da Silva
Source: Tetrahedron Letters. Unidade: FCFRP
Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO, FÁRMACOS
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ABNT
FRANCO, Márcia Silvana Freire et al. Palladium-catalyzed C–H alkenylation of quinoxaline N-oxide enabled by a mono-N-protected amino acid. Tetrahedron Letters, v. 59, n. 26, p. 2562-2566, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2018.05.054. Acesso em: 27 jun. 2024.
APA
Franco, M. S. F., Paula, M. H. de, Glowacka, P. C., Fumagalli, F., Clososki, G. C., & Emery, F. da S. (2018). Palladium-catalyzed C–H alkenylation of quinoxaline N-oxide enabled by a mono-N-protected amino acid. Tetrahedron Letters, 59( 26), 2562-2566. doi:10.1016/j.tetlet.2018.05.054
NLM
Franco MSF, Paula MH de, Glowacka PC, Fumagalli F, Clososki GC, Emery F da S. Palladium-catalyzed C–H alkenylation of quinoxaline N-oxide enabled by a mono-N-protected amino acid [Internet]. Tetrahedron Letters. 2018 ; 59( 26): 2562-2566.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2018.05.054
Vancouver
Franco MSF, Paula MH de, Glowacka PC, Fumagalli F, Clososki GC, Emery F da S. Palladium-catalyzed C–H alkenylation of quinoxaline N-oxide enabled by a mono-N-protected amino acid [Internet]. Tetrahedron Letters. 2018 ; 59( 26): 2562-2566.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2018.05.054
Artigo de periodico
Absolute configurations of griseorhodins A and C (2017)
Ortega, Humberto E.; Batista, João M.; Melo, Weilan G.P.; Clardy, Jon; Pupo, Mônica Tallarico
Source: Tetrahedron Letters. Unidade: FCFRP
Subjects: STREPTOMYCES, ANTIBIÓTICOS, QUÍMICA FARMACÊUTICA
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ABNT
ORTEGA, Humberto E. et al. Absolute configurations of griseorhodins A and C. Tetrahedron Letters, v. 58, n. 50, p. 4721-4723, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.11.008. Acesso em: 27 jun. 2024.
APA
Ortega, H. E., Batista, J. M., Melo, W. G. P., Clardy, J., & Pupo, M. T. (2017). Absolute configurations of griseorhodins A and C. Tetrahedron Letters, 58( 50), 4721-4723. doi:10.1016/j.tetlet.2017.11.008
NLM
Ortega HE, Batista JM, Melo WGP, Clardy J, Pupo MT. Absolute configurations of griseorhodins A and C [Internet]. Tetrahedron Letters. 2017 ; 58( 50): 4721-4723.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2017.11.008
Vancouver
Ortega HE, Batista JM, Melo WGP, Clardy J, Pupo MT. Absolute configurations of griseorhodins A and C [Internet]. Tetrahedron Letters. 2017 ; 58( 50): 4721-4723.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2017.11.008
Artigo de periodico
New perylenequinone derivatives from the endophytic fungus Alternaria tenuissima SS77 (2016)
Chagas, Fernanda O; Dias, Luís Gustavo; Pupo, Mônica Tallarico
Source: Tetrahedron Letters. Unidades: FFCLRP, FCFRP
Subjects: FUNGOS, PRODUTOS NATURAIS, MICOTOXINAS, METABÓLITOS SECUNDÁRIOS
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ABNT
CHAGAS, Fernanda O e DIAS, Luís Gustavo e PUPO, Mônica Tallarico. New perylenequinone derivatives from the endophytic fungus Alternaria tenuissima SS77. Tetrahedron Letters, v. 57, n. 29, p. 3185-3189, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.06.035. Acesso em: 27 jun. 2024.
APA
Chagas, F. O., Dias, L. G., & Pupo, M. T. (2016). New perylenequinone derivatives from the endophytic fungus Alternaria tenuissima SS77. Tetrahedron Letters, 57( 29), 3185-3189. doi:10.1016/j.tetlet.2016.06.035
NLM
Chagas FO, Dias LG, Pupo MT. New perylenequinone derivatives from the endophytic fungus Alternaria tenuissima SS77 [Internet]. Tetrahedron Letters. 2016 ; 57( 29): 3185-3189.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2016.06.035
Vancouver
Chagas FO, Dias LG, Pupo MT. New perylenequinone derivatives from the endophytic fungus Alternaria tenuissima SS77 [Internet]. Tetrahedron Letters. 2016 ; 57( 29): 3185-3189.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2016.06.035
Artigo de periodico
Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes (2016)
Glowacka, Paulina C.; Maindron, Nicolas; Stephenson, G. Richard; Romieu, Anthony; Renard, Pierre-Yves; Emery, Flavio da Silva
Source: Tetrahedron Letters. Unidade: FCFRP
Subjects: FLUORESCÊNCIA, COMPOSTOS ORGÂNICOS
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ABNT
GLOWACKA, Paulina C. et al. Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes. Tetrahedron Letters, v. 57, n. 45, p. 4991-4996, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.09.091. Acesso em: 27 jun. 2024.
APA
Glowacka, P. C., Maindron, N., Stephenson, G. R., Romieu, A., Renard, P. -Y., & Emery, F. da S. (2016). Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes. Tetrahedron Letters, 57( 45), 4991-4996. doi:10.1016/j.tetlet.2016.09.091
NLM
Glowacka PC, Maindron N, Stephenson GR, Romieu A, Renard P-Y, Emery F da S. Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes [Internet]. Tetrahedron Letters. 2016 ; 57( 45): 4991-4996.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2016.09.091
Vancouver
Glowacka PC, Maindron N, Stephenson GR, Romieu A, Renard P-Y, Emery F da S. Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes [Internet]. Tetrahedron Letters. 2016 ; 57( 45): 4991-4996.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2016.09.091
Artigo de periodico
A novel labdane diterpene from Acritopappus longifolius (2011)
Ferreira, Fernanda Peres; Marturano, Eduardo Henck; Carollo, Carlos Alexandre; Oliveira, Dionéia Camilo Rodrigues de
Source: Tetrahedron Letters. Unidade: FCFRP
Subjects: COMPOSITAE, QUÍMICA ORGÂNICA, ESPECTROSCOPIA DE MASSA
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ABNT
FERREIRA, Fernanda Peres et al. A novel labdane diterpene from Acritopappus longifolius. Tetrahedron Letters, v. 52, n. 2, p. 297-299, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2010.11.040. Acesso em: 27 jun. 2024.
APA
Ferreira, F. P., Marturano, E. H., Carollo, C. A., & Oliveira, D. C. R. de. (2011). A novel labdane diterpene from Acritopappus longifolius. Tetrahedron Letters, 52( 2), 297-299. doi:10.1016/j.tetlet.2010.11.040
NLM
Ferreira FP, Marturano EH, Carollo CA, Oliveira DCR de. A novel labdane diterpene from Acritopappus longifolius [Internet]. Tetrahedron Letters. 2011 ; 52( 2): 297-299.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2010.11.040
Vancouver
Ferreira FP, Marturano EH, Carollo CA, Oliveira DCR de. A novel labdane diterpene from Acritopappus longifolius [Internet]. Tetrahedron Letters. 2011 ; 52( 2): 297-299.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2010.11.040
Artigo de periodico
Tandem reduction + cyclization of ortho-substituted cinnamic esters (2011)
Sass, Daiane Cristina; Lucca Júnior, Emílio Carlos de; Barbosa, Jader da Silva; Oliveira, Kleber Thiago de; Constantino, Maurício Gomes
Source: Tetrahedron Letters. Unidade: FFCLRP
Assunto: QUÍMICA
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ABNT
SASS, Daiane Cristina et al. Tandem reduction + cyclization of ortho-substituted cinnamic esters. Tetrahedron Letters, v. 52, n. 41, p. 5371-5374, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.08.039. Acesso em: 27 jun. 2024.
APA
Sass, D. C., Lucca Júnior, E. C. de, Barbosa, J. da S., Oliveira, K. T. de, & Constantino, M. G. (2011). Tandem reduction + cyclization of ortho-substituted cinnamic esters. Tetrahedron Letters, 52( 41), 5371-5374. doi:10.1016/j.tetlet.2011.08.039
NLM
Sass DC, Lucca Júnior EC de, Barbosa J da S, Oliveira KT de, Constantino MG. Tandem reduction + cyclization of ortho-substituted cinnamic esters [Internet]. Tetrahedron Letters. 2011 ; 52( 41): 5371-5374.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2011.08.039
Vancouver
Sass DC, Lucca Júnior EC de, Barbosa J da S, Oliveira KT de, Constantino MG. Tandem reduction + cyclization of ortho-substituted cinnamic esters [Internet]. Tetrahedron Letters. 2011 ; 52( 41): 5371-5374.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2011.08.039
Artigo de periodico
Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator (2011)
Nazario, Carlos E. D.; Santana, Amanda S.; Kawasoko, Cristiane Y.; Carollo, Carlos A.; Hurtado, Gabriela R.; Viana, Luiz H.; Barbosa, Sandro L.; Guerrero Junior, Palimécio G.; Marques, Francisco A.; Dabdoub, Vânia B.; Dabdoub, Miguel Joaquim; Baroni, Adriano C. M.
Source: Tetrahedron Letters. Unidade: FFCLRP
Assunto: QUÍMICA
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ABNT
NAZARIO, Carlos E. D. et al. Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator. Tetrahedron Letters, v. 52, n. 32, p. 4177-4181, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.06.004. Acesso em: 27 jun. 2024.
APA
Nazario, C. E. D., Santana, A. S., Kawasoko, C. Y., Carollo, C. A., Hurtado, G. R., Viana, L. H., et al. (2011). Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator. Tetrahedron Letters, 52( 32), 4177-4181. doi:10.1016/j.tetlet.2011.06.004
NLM
Nazario CED, Santana AS, Kawasoko CY, Carollo CA, Hurtado GR, Viana LH, Barbosa SL, Guerrero Junior PG, Marques FA, Dabdoub VB, Dabdoub MJ, Baroni ACM. Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator [Internet]. Tetrahedron Letters. 2011 ; 52( 32): 4177-4181.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2011.06.004
Vancouver
Nazario CED, Santana AS, Kawasoko CY, Carollo CA, Hurtado GR, Viana LH, Barbosa SL, Guerrero Junior PG, Marques FA, Dabdoub VB, Dabdoub MJ, Baroni ACM. Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator [Internet]. Tetrahedron Letters. 2011 ; 52( 32): 4177-4181.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2011.06.004
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: 27 jun. 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 jun. 27 ] 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 jun. 27 ] 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: 27 jun. 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 jun. 27 ]
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 jun. 27 ]
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: 27 jun. 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 jun. 27 ] 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 jun. 27 ] 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: 27 jun. 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 jun. 27 ] 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 jun. 27 ] 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: 27 jun. 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 jun. 27 ] 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 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
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: 27 jun. 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 jun. 27 ] 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 jun. 27 ] 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: 27 jun. 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 jun. 27 ] 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 jun. 27 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 27 jun. 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 jun. 27 ] 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 jun. 27 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 27 jun. 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 jun. 27 ]
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 jun. 27 ]
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)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 27 jun. 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 jun. 27 ]
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 jun. 27 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 27 jun. 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 jun. 27 ] 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 jun. 27 ] 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: 27 jun. 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 jun. 27 ]
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 jun. 27 ]
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: 27 jun. 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 jun. 27 ] 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 jun. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.129

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