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  • Source: Tetrahedron Letters. Unidade: FCFRP

    Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO, FÁRMACOS

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      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: http://dx.doi.org/10.1016/j.tetlet.2018.05.054. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2018.05.054
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: ITÉRBIO, SÍNTESE ORGÂNICA

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      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: http://dx.doi.org/10.1016/j.tetlet.2018.09.022. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2018.09.022
  • Source: Tetrahedron Letters. Unidades: FFCLRP, FCFRP

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, PRODUTOS NATURAIS

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      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: http://dx.doi.org/10.1016/j.tetlet.2017.09.051. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2017.09.051
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, COBRE

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      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: http://dx.doi.org/10.1016/j.tetlet.2017.01.059. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2017.01.059
  • Source: Tetrahedron Letters. Unidade: FCFRP

    Subjects: STREPTOMYCES, ANTIBIÓTICOS, QUÍMICA FARMACÊUTICA

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      ORTEGA, Humberto E. et al. Absolute configurations of griseorhodins A and C. Tetrahedron Letters, v. 58, n. 50, p. 4721-4723, 2017Tradução . . Disponível em: http://dx.doi.org/10.1016/j.tetlet.2017.11.008. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2017.11.008
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, COBRE

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      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: http://dx.doi.org/10.1016/j.tetlet.2017.01.107. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2017.01.107
  • Source: Tetrahedron Letters. Unidades: FFCLRP, FCFRP

    Subjects: FUNGOS, PRODUTOS NATURAIS, MICOTOXINAS, METABÓLITOS SECUNDÁRIOS

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      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: http://dx.doi.org/10.1016/j.tetlet.2016.06.035. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2016.06.035
  • Source: Tetrahedron Letters. Unidade: FCFRP

    Subjects: FLUORESCÊNCIA, COMPOSTOS ORGÂNICOS

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      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: http://dx.doi.org/10.1016/j.tetlet.2016.09.091. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2016.09.091
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: TECNOLOGIA DE MICRO-ONDAS, ALDEÍDOS

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      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: http://dx.doi.org/10.1016/j.tetlet.2016.02.105. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2016.02.105
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO

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      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: http://dx.doi.org/10.1016/j.tetlet.2015.08.052. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2015.08.052
  • Source: Tetrahedron Letters. Unidade: FCFRP

    Subjects: ALCALOIDES, PALÁDIO, CATALISADORES, PRODUTOS NATURAIS

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      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: http://dx.doi.org/10.1016/j.tetlet.2015.03.039. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2015.03.039
  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      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: http://dx.doi.org/10.1016/j.tetlet.2015.05.066. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2015.05.066
  • Source: Tetrahedron Letters. Unidade: FCFRP

    Subjects: CUCURBITALES, GLICOSÍDEOS, BIOLOGIA CELULAR

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      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: http://dx.doi.org/10.1016/j.tetlet.2014.11.049. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2014.11.049
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: AMINAS, CATÁLISE

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      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: http://dx.doi.org/10.1016/j.tetlet.2015.01.059. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2015.01.059
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      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: http://dx.doi.org/10.1016/j.tetlet.2015.06.061. Acesso em: 07 fev. 2023.
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      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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2015.06.061
  • Source: Tetrahedron Letters. Unidade: IQSC

    Assunto: FÍSICO-QUÍMICA

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    • 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: http://dx.doi.org/10.1016/j.tetlet.2015.02.046. Acesso em: 07 fev. 2023.
    • 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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2015.02.046
  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      STEFANI, Hélio Alexandre et al. Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, v. 55, n. 31, p. 4355-4358, 2014Tradução . . Disponível em: http://dx.doi.org/10.1016/j.tetlet.2014.05.095. Acesso em: 07 fev. 2023.
    • 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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2014.05.095
  • Source: Tetrahedron Letters. Unidades: FCFRP, IQSC

    Subjects: ENZIMAS, QUÍMICA ORGÂNICA

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    • 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: http://dx.doi.org/10.1016/j.tetlet.2014.07.032. Acesso em: 07 fev. 2023.
    • 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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2014.07.032
  • 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: http://dx.doi.org/10.1016/j.tetlet.2014.02.113. Acesso em: 07 fev. 2023.
    • 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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2014.02.113
  • Source: Tetrahedron Letters. Unidade: FCFRP

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, PRODUTOS NATURAIS

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    • 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: http://dx.doi.org/10.1016/j.tetlet.2012.12.062. Acesso em: 07 fev. 2023.
    • APA

      Leoneti, V. A., & Carvalho, I. (2013). Simple and efficient synthesis of 2,5-anhydro-D-glucitol. Tetrahedron Letters, 54, 1087-1089. Recuperado de http://dx.doi.org/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 2023 fev. 07 ] Available from: http://dx.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 2023 fev. 07 ] Available from: http://dx.doi.org/10.1016/j.tetlet.2012.12.062

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