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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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2018.05.054
Artigo de periodico
Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted (2018)
Oliveira, Isadora M. de; Darbem, Mariana P; Esteves, Carlos Henrique Alves; Pimenta, Daniel C; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: Tetrahedron Letters. Unidade: FCF
Subjects: ITÉRBIO, SÍNTESE ORGÂNICA
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ABNT
OLIVEIRA, Isadora M. de et al. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted. Tetrahedron Letters, v. 59, n. 24, p. 3907-3911, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2018.09.022. Acesso em: 10 nov. 2024.
APA
Oliveira, I. M. de, Darbem, M. P., Esteves, C. H. A., Pimenta, D. C., Schpector, J. Z., Stefani, H. A., & Manarin, F. (2018). Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted. Tetrahedron Letters, 59( 24), 3907-3911. doi:10.1016/j.tetlet.2018.09.022
NLM
Oliveira IM de, Darbem MP, Esteves CHA, Pimenta DC, Schpector JZ, Stefani HA, Manarin F. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted [Internet]. Tetrahedron Letters. 2018 ; 59( 24): 3907-3911.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
Vancouver
Oliveira IM de, Darbem MP, Esteves CHA, Pimenta DC, Schpector JZ, Stefani HA, Manarin F. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted [Internet]. Tetrahedron Letters. 2018 ; 59( 24): 3907-3911.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
Artigo de periodico
Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl (2017)
Bozzini, Leandro A; Batista, João H. C.; Mello, Murilo B. M. de; Vessecchi, Ricardo; Clososki, Giuliano Cesar
Source: Tetrahedron Letters. Unidades: FFCLRP, FCFRP
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, PRODUTOS NATURAIS
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ABNT
BOZZINI, Leandro A et al. Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl. Tetrahedron Letters, v. 58, p. 4186-4190, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.09.051. Acesso em: 10 nov. 2024.
APA
Bozzini, L. A., Batista, J. H. C., Mello, M. B. M. de, Vessecchi, R., & Clososki, G. C. (2017). Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl. Tetrahedron Letters, 58, 4186-4190. doi:10.1016/j.tetlet.2017.09.051
NLM
Bozzini LA, Batista JHC, Mello MBM de, Vessecchi R, Clososki GC. Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl [Internet]. Tetrahedron Letters. 2017 ; 58 4186-4190.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2017.09.051
Vancouver
Bozzini LA, Batista JHC, Mello MBM de, Vessecchi R, Clososki GC. Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl [Internet]. Tetrahedron Letters. 2017 ; 58 4186-4190.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2017.09.051
Artigo de periodico
Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization (2017)
Shamim, Anwar; Souza, Frederico Bernardes de; Vasconcelos, Stanley Nunes Siqueira; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, COBRE
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ABNT
SHAMIM, Anwar et al. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, v. 58, n. 9, p. 884-888, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.01.059. Acesso em: 10 nov. 2024.
APA
Shamim, A., Souza, F. B. de, Vasconcelos, S. N. S., & Stefani, H. A. (2017). Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, 58( 9), 884-888. doi:10.1016/j.tetlet.2017.01.059
NLM
Shamim A, Souza FB de, Vasconcelos SNS, Stefani HA. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization [Internet]. Tetrahedron Letters. 2017 ; 58( 9): 884-888.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059
Vancouver
Shamim A, Souza FB de, Vasconcelos SNS, Stefani HA. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization [Internet]. Tetrahedron Letters. 2017 ; 58( 9): 884-888.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059
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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2017.11.008
Artigo de periodico
Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition (2017)
Souza, Frederico Bernardes de; Vasconcelos, Stanley Nunes Siqueira; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, COBRE
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ABNT
SOUZA, Frederico Bernardes de et al. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition. Tetrahedron Letters, v. 58, n. 11, p. 1057-1060, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.01.107. Acesso em: 10 nov. 2024.
APA
Souza, F. B. de, Vasconcelos, S. N. S., Reis, J. S. dos, Pimenta, D. C., & Stefani, H. A. (2017). Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition. Tetrahedron Letters, 58( 11), 1057-1060. doi:10.1016/j.tetlet.2017.01.107
NLM
Souza FB de, Vasconcelos SNS, Reis JS dos, Pimenta DC, Stefani HA. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition [Internet]. Tetrahedron Letters. 2017 ; 58( 11): 1057-1060.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.107
Vancouver
Souza FB de, Vasconcelos SNS, Reis JS dos, Pimenta DC, Stefani HA. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition [Internet]. Tetrahedron Letters. 2017 ; 58( 11): 1057-1060.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.107
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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2016.09.091
Artigo de periodico
Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles (2016)
Souza, Frederico B; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: TECNOLOGIA DE MICRO-ONDAS, ALDEÍDOS
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ABNT
SOUZA, Frederico B e PIMENTA, Daniel Carvalho e STEFANI, Hélio Alexandre. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles. Tetrahedron Letters, v. 57, n. 14, p. 1592-1596, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.02.105. Acesso em: 10 nov. 2024.
APA
Souza, F. B., Pimenta, D. C., & Stefani, H. A. (2016). Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles. Tetrahedron Letters, 57( 14), 1592-1596. doi:10.1016/j.tetlet.2016.02.105
NLM
Souza FB, Pimenta DC, Stefani HA. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles [Internet]. Tetrahedron Letters. 2016 ; 57( 14): 1592-1596.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2016.02.105
Vancouver
Souza FB, Pimenta DC, Stefani HA. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles [Internet]. Tetrahedron Letters. 2016 ; 57( 14): 1592-1596.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2016.02.105
Artigo de periodico
Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine (2015)
Fumagalli, Fernando; Emery, Flavio da Silva
Source: Tetrahedron Letters. Unidade: FCFRP
Subjects: ALCALOIDES, PALÁDIO, CATALISADORES, PRODUTOS NATURAIS
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ABNT
FUMAGALLI, Fernando e EMERY, Flavio da Silva. Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine. Tetrahedron Letters, v. 56, n. 18, p. 2307-2310, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.03.039. Acesso em: 10 nov. 2024.
APA
Fumagalli, F., & Emery, F. da S. (2015). Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine. Tetrahedron Letters, 56( 18), 2307-2310. doi:10.1016/j.tetlet.2015.03.039
NLM
Fumagalli F, Emery F da S. Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine [Internet]. Tetrahedron Letters. 2015 ; 56( 18): 2307-2310.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.03.039
Vancouver
Fumagalli F, Emery F da S. Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine [Internet]. Tetrahedron Letters. 2015 ; 56( 18): 2307-2310.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.03.039
Artigo de periodico
Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization (2015)
Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Ali, Bakhat; Madureira, Lucas Sousa; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO
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ABNT
SHAMIM, Anwar et al. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, v. 56, n. 43, p. 5836-5842, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.08.052. Acesso em: 10 nov. 2024.
APA
Shamim, A., Vasconcelos, S. N. S., Ali, B., Madureira, L. S., Zukerman-Schpector, J., & Stefani, H. A. (2015). Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, 56( 43), 5836-5842. doi:10.1016/j.tetlet.2015.08.052
NLM
Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
Vancouver
Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
Artigo de periodico
Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones (2015)
Ali, Bakhat; Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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ABNT
ALI, Bakhat et al. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, v. 56, n. 28, p. 4234-4241, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.05.066. Acesso em: 10 nov. 2024.
APA
Ali, B., Shamim, A., Vasconcelos, S. N. S., & Stefani, H. A. (2015). Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, 56( 28), 4234-4241. doi:10.1016/j.tetlet.2015.05.066
NLM
Ali B, Shamim A, Vasconcelos SNS, Stefani HA. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones [Internet]. Tetrahedron Letters. 2015 ; 56( 28): 4234-4241.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066
Vancouver
Ali B, Shamim A, Vasconcelos SNS, Stefani HA. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones [Internet]. Tetrahedron Letters. 2015 ; 56( 28): 4234-4241.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066
Artigo de periodico
Semi-synthesis of new glycosidic triazole derivates of dihydrocucurbitacin B (2015)
Morotti, Ana L. M.; Lang, Karen L.; Carvalho, Ivone; Schenkel, Eloir P.; Bernardes, Lílian S. C.
Source: Tetrahedron Letters. Unidade: FCFRP
Subjects: CUCURBITALES, GLICOSÍDEOS, BIOLOGIA CELULAR
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ABNT
MOROTTI, Ana L. M. et al. Semi-synthesis of new glycosidic triazole derivates of dihydrocucurbitacin B. Tetrahedron Letters, v. 56, n. 2, p. 303-307, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2014.11.049. Acesso em: 10 nov. 2024.
APA
Morotti, A. L. M., Lang, K. L., Carvalho, I., Schenkel, E. P., & Bernardes, L. S. C. (2015). Semi-synthesis of new glycosidic triazole derivates of dihydrocucurbitacin B. Tetrahedron Letters, 56( 2), 303-307. doi:10.1016/j.tetlet.2014.11.049
NLM
Morotti ALM, Lang KL, Carvalho I, Schenkel EP, Bernardes LSC. Semi-synthesis of new glycosidic triazole derivates of dihydrocucurbitacin B [Internet]. Tetrahedron Letters. 2015 ; 56( 2): 303-307.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2014.11.049
Vancouver
Morotti ALM, Lang KL, Carvalho I, Schenkel EP, Bernardes LSC. Semi-synthesis of new glycosidic triazole derivates of dihydrocucurbitacin B [Internet]. Tetrahedron Letters. 2015 ; 56( 2): 303-307.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2014.11.049
Artigo de periodico
Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes (2015)
Ali, Bakhat; Schpector, Júlio Zukerman; Ferreira, Fernando P; Shamim, Anwar; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: AMINAS, CATÁLISE
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ABNT
ALI, Bakhat et al. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, v. 56, n. 9, p. 1153-1158, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.01.059. Acesso em: 10 nov. 2024.
APA
Ali, B., Schpector, J. Z., Ferreira, F. P., Shamim, A., Pimenta, D. C., & Stefani, H. A. (2015). Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, 56( 9), 1153-1158. doi:10.1016/j.tetlet.2015.01.059
NLM
Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
Vancouver
Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
Artigo de periodico
One-step synthesis of indanones through NbCl5-induced Friedel-Crafts reaction (2015)
Barbosa, Jader da Silva; Silva, Gil Valdo José da; Constantino, Maurício Gomes
Source: Tetrahedron Letters. Unidade: FFCLRP
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARBOSA, Jader da Silva e SILVA, Gil Valdo José da e CONSTANTINO, Maurício Gomes. One-step synthesis of indanones through NbCl5-induced Friedel-Crafts reaction. Tetrahedron Letters, v. 56, n. 32, p. 4649-4652, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.06.061. Acesso em: 10 nov. 2024.
APA
Barbosa, J. da S., Silva, G. V. J. da, & Constantino, M. G. (2015). One-step synthesis of indanones through NbCl5-induced Friedel-Crafts reaction. Tetrahedron Letters, 56( 32), 4649-4652. doi:10.1016/j.tetlet.2015.06.061
NLM
Barbosa J da S, Silva GVJ da, Constantino MG. One-step synthesis of indanones through NbCl5-induced Friedel-Crafts reaction [Internet]. Tetrahedron Letters. 2015 ; 56( 32): 4649-4652.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.06.061
Vancouver
Barbosa J da S, Silva GVJ da, Constantino MG. One-step synthesis of indanones through NbCl5-induced Friedel-Crafts reaction [Internet]. Tetrahedron Letters. 2015 ; 56( 32): 4649-4652.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.06.061
Artigo de periodico
Synthesis and enzymatic resolution of racemic 2,3-epoxy propyl esters obtained from glycerol (2015)
Araujo, Yara Jaqueline Kerber; Avvari, Naga Prasad; Paiva, Derisvaldo Rosa; Lima, Dênis Pires de; Beatriz, Adilson
Source: Tetrahedron Letters. Unidade: IQSC
Assunto: FÍSICO-QUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARAUJO, Yara Jaqueline Kerber et al. Synthesis and enzymatic resolution of racemic 2,3-epoxy propyl esters obtained from glycerol. Tetrahedron Letters, v. 56, n. 13, p. 1696-1698, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.02.046. Acesso em: 10 nov. 2024.
APA
Araujo, Y. J. K., Avvari, N. P., Paiva, D. R., Lima, D. P. de, & Beatriz, A. (2015). Synthesis and enzymatic resolution of racemic 2,3-epoxy propyl esters obtained from glycerol. Tetrahedron Letters, 56( 13), 1696-1698. doi:10.1016/j.tetlet.2015.02.046
NLM
Araujo YJK, Avvari NP, Paiva DR, Lima DP de, Beatriz A. Synthesis and enzymatic resolution of racemic 2,3-epoxy propyl esters obtained from glycerol [Internet]. Tetrahedron Letters. 2015 ; 56( 13): 1696-1698.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.02.046
Vancouver
Araujo YJK, Avvari NP, Paiva DR, Lima DP de, Beatriz A. Synthesis and enzymatic resolution of racemic 2,3-epoxy propyl esters obtained from glycerol [Internet]. Tetrahedron Letters. 2015 ; 56( 13): 1696-1698.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.02.046
Artigo de periodico
Synthesis of functionalized N-triazolyl maleimides (2014)
Stefani, Hélio Alexandre ; Ferreira, Fernando P; Ali, Bakhat; Pimenta, Daniel Carvalho
Source: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, v. 55, n. 31, p. 4355-4358, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2014.05.095. Acesso em: 10 nov. 2024.
APA
Stefani, H. A., Ferreira, F. P., Ali, B., & Pimenta, D. C. (2014). Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, 55( 31), 4355-4358. doi:10.1016/j.tetlet.2014.05.095
NLM
Stefani HA, Ferreira FP, Ali B, Pimenta DC. Synthesis of functionalized N-triazolyl maleimides [Internet]. Tetrahedron Letters. 2014 ; 55( 31): 4355-4358.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095
Vancouver
Stefani HA, Ferreira FP, Ali B, Pimenta DC. Synthesis of functionalized N-triazolyl maleimides [Internet]. Tetrahedron Letters. 2014 ; 55( 31): 4355-4358.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095
Artigo de periodico
Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres (2014)
Ferreira , Irlon Maciel; Nishimura, Rodolfo H. V.; Souza, Ana Beatriz dos A; Clososki, Giuliano Cesar; Yoshioka, Sergio Akinobu ; Porto, Andre Luiz Meleiro
Source: Tetrahedron Letters. Unidades: FCFRP, IQSC
Subjects: ENZIMAS, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA , Irlon Maciel et al. Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres. Tetrahedron Letters, v. 55, n. 7, p. 5062-5065, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2014.07.032. Acesso em: 10 nov. 2024.
APA
Ferreira , I. M., Nishimura, R. H. V., Souza, A. B. dos A., Clososki, G. C., Yoshioka, S. A., & Porto, A. L. M. (2014). Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres. Tetrahedron Letters, 55( 7), 5062-5065. doi:10.1016/j.tetlet.2014.07.032
NLM
Ferreira IM, Nishimura RHV, Souza AB dos A, Clososki GC, Yoshioka SA, Porto ALM. Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres [Internet]. Tetrahedron Letters. 2014 ; 55( 7): 5062-5065.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2014.07.032
Vancouver
Ferreira IM, Nishimura RHV, Souza AB dos A, Clososki GC, Yoshioka SA, Porto ALM. Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres [Internet]. Tetrahedron Letters. 2014 ; 55( 7): 5062-5065.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2014.07.032
Artigo de periodico
Simple and efﬁcient synthesis of 2,5-anhydro-D-glucitol (2013)
Leoneti, Valquiria Aragão; Carvalho, Ivone
Source: Tetrahedron Letters. Unidade: FCFRP
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, PRODUTOS NATURAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEONETI, Valquiria Aragão e CARVALHO, Ivone. Simple and efﬁcient synthesis of 2,5-anhydro-D-glucitol. Tetrahedron Letters, v. 54, p. 1087-1089, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.12.062. Acesso em: 10 nov. 2024.
APA
Leoneti, V. A., & Carvalho, I. (2013). Simple and efﬁcient synthesis of 2,5-anhydro-D-glucitol. Tetrahedron Letters, 54, 1087-1089. doi:10.1016/j.tetlet.2012.12.062
NLM
Leoneti VA, Carvalho I. Simple and efﬁcient synthesis of 2,5-anhydro-D-glucitol [Internet]. Tetrahedron Letters. 2013 ; 54 1087-1089.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2012.12.062
Vancouver
Leoneti VA, Carvalho I. Simple and efﬁcient synthesis of 2,5-anhydro-D-glucitol [Internet]. Tetrahedron Letters. 2013 ; 54 1087-1089.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2012.12.062
Artigo de periodico
Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction (2013)
Stefani, Hélio Alexandre ; Silva, Nathália Cristina da Silva e; Vasconcelos, Stanley Nunes Siqueira; Manarin, Flávia; Souza, Frederico B
Source: Tetrahedron Letters. Unidade: FCF
Subjects: TELÚRIO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction. Tetrahedron Letters, v. 54, n. 22, p. 2809-2812, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.03.061. Acesso em: 10 nov. 2024.
APA
Stefani, H. A., Silva, N. C. da S. e, Vasconcelos, S. N. S., Manarin, F., & Souza, F. B. (2013). Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction. Tetrahedron Letters, 54( 22), 2809-2812. doi:10.1016/j.tetlet.2013.03.061
NLM
Stefani HA, Silva NC da S e, Vasconcelos SNS, Manarin F, Souza FB. Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction [Internet]. Tetrahedron Letters. 2013 ; 54( 22): 2809-2812.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2013.03.061
Vancouver
Stefani HA, Silva NC da S e, Vasconcelos SNS, Manarin F, Souza FB. Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction [Internet]. Tetrahedron Letters. 2013 ; 54( 22): 2809-2812.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2013.03.061

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