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  • Source: Marine Biotechnology. Unidade: IQSC

    Subjects: BIOTRANSFORMAÇÃO, SÍNTESE ORGÂNICA

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    • ABNT

      MATOS, Iara Lisboa de e NITSCHKE, Marcia e PORTO, Andre Luiz Meleiro. Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii. Marine Biotechnology, v. 21, p. 430-439 jun, 2019Tradução . . Disponível em: https://doi.org/10.1007/s10126-019-09893-y. Acesso em: 02 out. 2024.
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      Matos, I. L. de, Nitschke, M., & Porto, A. L. M. (2019). Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii. Marine Biotechnology, 21, 430-439 jun. doi:10.1007/s10126-019-09893-y
    • NLM

      Matos IL de, Nitschke M, Porto ALM. Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii [Internet]. Marine Biotechnology. 2019 ; 21 430-439 jun.[citado 2024 out. 02 ] Available from: https://doi.org/10.1007/s10126-019-09893-y
    • Vancouver

      Matos IL de, Nitschke M, Porto ALM. Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii [Internet]. Marine Biotechnology. 2019 ; 21 430-439 jun.[citado 2024 out. 02 ] Available from: https://doi.org/10.1007/s10126-019-09893-y
  • Source: Synthetic Communications. Unidade: FFCLRP

    Assunto: SÍNTESE ORGÂNICA

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      CONSTANTINO, Maurício Gomes et al. Opening of epoxide rings catalyzed by niobium pentachloride. Synthetic Communications, v. 37, p. 3529-3539, 2007Tradução . . Acesso em: 02 out. 2024.
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      Constantino, M. G., Lacerda Júnior, V., Invernize, P. R., Silva Filho, L. C. da, & Silva, G. V. J. da. (2007). Opening of epoxide rings catalyzed by niobium pentachloride. Synthetic Communications, 37, 3529-3539.
    • NLM

      Constantino MG, Lacerda Júnior V, Invernize PR, Silva Filho LC da, Silva GVJ da. Opening of epoxide rings catalyzed by niobium pentachloride. Synthetic Communications. 2007 ; 37 3529-3539.[citado 2024 out. 02 ]
    • Vancouver

      Constantino MG, Lacerda Júnior V, Invernize PR, Silva Filho LC da, Silva GVJ da. Opening of epoxide rings catalyzed by niobium pentachloride. Synthetic Communications. 2007 ; 37 3529-3539.[citado 2024 out. 02 ]
  • Source: Spectrochimica Acta Part A. Unidade: FFCLRP

    Assunto: SÍNTESE ORGÂNICA

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      OLIVEIRA, Kleber Thiago de et al. Analysis of a cycloheptenone derivative: an experimental and theoretical approach. Spectrochimica Acta Part A, v. 63, p. 709-713, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.saa.2005.06.023. Acesso em: 02 out. 2024.
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      Oliveira, K. T. de, Lacerda Júnior, V., Constantino, M. G., Donate, P. M., Silva, G. V. J. da, Brocksom, T. J., & Frederico, D. (2006). Analysis of a cycloheptenone derivative: an experimental and theoretical approach. Spectrochimica Acta Part A, 63, 709-713. doi:10.1016/j.saa.2005.06.023
    • NLM

      Oliveira KT de, Lacerda Júnior V, Constantino MG, Donate PM, Silva GVJ da, Brocksom TJ, Frederico D. Analysis of a cycloheptenone derivative: an experimental and theoretical approach [Internet]. Spectrochimica Acta Part A. 2006 ; 63 709-713.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.saa.2005.06.023
    • Vancouver

      Oliveira KT de, Lacerda Júnior V, Constantino MG, Donate PM, Silva GVJ da, Brocksom TJ, Frederico D. Analysis of a cycloheptenone derivative: an experimental and theoretical approach [Internet]. Spectrochimica Acta Part A. 2006 ; 63 709-713.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.saa.2005.06.023
  • Source: Magnetic Resonance in Chemistry. Unidade: FFCLRP

    Assunto: SÍNTESE ORGÂNICA

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      CONSTANTINO, Maurício Gomes e LACERDA JÚNIOR, Valdemar e SILVA, Gil Valdo José da. Spectral assignments and reference data: detailed assignments of'H ANT POT 1'and Ç ANT POT 13' NMR spectral data of '13 beta-substituted' cycloenones. Magnetic Resonance in Chemistry, v. 43, p. 346-347, 2005Tradução . . Acesso em: 02 out. 2024.
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      Constantino, M. G., Lacerda Júnior, V., & Silva, G. V. J. da. (2005). Spectral assignments and reference data: detailed assignments of'H ANT POT 1'and Ç ANT POT 13' NMR spectral data of '13 beta-substituted' cycloenones. Magnetic Resonance in Chemistry, 43, 346-347.
    • NLM

      Constantino MG, Lacerda Júnior V, Silva GVJ da. Spectral assignments and reference data: detailed assignments of'H ANT POT 1'and Ç ANT POT 13' NMR spectral data of '13 beta-substituted' cycloenones. Magnetic Resonance in Chemistry. 2005 ; 43 346-347.[citado 2024 out. 02 ]
    • Vancouver

      Constantino MG, Lacerda Júnior V, Silva GVJ da. Spectral assignments and reference data: detailed assignments of'H ANT POT 1'and Ç ANT POT 13' NMR spectral data of '13 beta-substituted' cycloenones. Magnetic Resonance in Chemistry. 2005 ; 43 346-347.[citado 2024 out. 02 ]
  • Source: Magnetic Resonance in Chemistry. Unidades: FFCLRP, FCFRP

    Subjects: SÍNTESE ORGÂNICA, PARASITOLOGIA

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      SILVA, Rosangela da et al. Complete assignment of the 'ANTPOT. 1 H' and 'ANTPOT. 13 C' NMR spectral data for benzylidenebenzyl butyrolactone. Magnetic Resonance in Chemistry, v. 43, p. 966-969, 2005Tradução . . Acesso em: 02 out. 2024.
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      Silva, R. da, Pedersoli, S., Lacerda Júnior, V., Donate, P. M., Albuquerque, S. de, Bastos, J. K., et al. (2005). Complete assignment of the 'ANTPOT. 1 H' and 'ANTPOT. 13 C' NMR spectral data for benzylidenebenzyl butyrolactone. Magnetic Resonance in Chemistry, 43, 966-969.
    • NLM

      Silva R da, Pedersoli S, Lacerda Júnior V, Donate PM, Albuquerque S de, Bastos JK, Araújo ALS de M, Silva MLA e. Complete assignment of the 'ANTPOT. 1 H' and 'ANTPOT. 13 C' NMR spectral data for benzylidenebenzyl butyrolactone. Magnetic Resonance in Chemistry. 2005 ; 43 966-969.[citado 2024 out. 02 ]
    • Vancouver

      Silva R da, Pedersoli S, Lacerda Júnior V, Donate PM, Albuquerque S de, Bastos JK, Araújo ALS de M, Silva MLA e. Complete assignment of the 'ANTPOT. 1 H' and 'ANTPOT. 13 C' NMR spectral data for benzylidenebenzyl butyrolactone. Magnetic Resonance in Chemistry. 2005 ; 43 966-969.[citado 2024 out. 02 ]
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, TELÚRIO

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      RAMINELLI, Cristiano et al. Coupling of butyl vinyl tellurides with metal acetylides catalyzed by nickel complexes. Tetrahedron Letters, v. 45, n. 25, p. 4927-4930, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2004.04.120. Acesso em: 02 out. 2024.
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      Raminelli, C., Gargalaka Júnior, J., Silveira, C. da C., & Comasseto, J. V. (2004). Coupling of butyl vinyl tellurides with metal acetylides catalyzed by nickel complexes. Tetrahedron Letters, 45( 25), 4927-4930. doi:10.1016/j.tetlet.2004.04.120
    • NLM

      Raminelli C, Gargalaka Júnior J, Silveira C da C, Comasseto JV. Coupling of butyl vinyl tellurides with metal acetylides catalyzed by nickel complexes [Internet]. Tetrahedron Letters. 2004 ; 45( 25): 4927-4930.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2004.04.120
    • Vancouver

      Raminelli C, Gargalaka Júnior J, Silveira C da C, Comasseto JV. Coupling of butyl vinyl tellurides with metal acetylides catalyzed by nickel complexes [Internet]. Tetrahedron Letters. 2004 ; 45( 25): 4927-4930.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetlet.2004.04.120
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, TELÚRIO, PALÁDIO, BIOQUÍMICA

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      ZENI, Gilson et al. 2,5-Bis-(butyltelluro) thiophene as a convenient precursor for the synthesis of 2,5-bis-(acetylenic) thiophenes. Tetrahedron Letters, v. 44, n. 4, p. 685-688, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0040-4039(02)02659-x. Acesso em: 02 out. 2024.
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      Zeni, G., Zeni, G., Nogueira, C. W., Silva, D. O., Menezes, P. H., Braga, A. L., et al. (2003). 2,5-Bis-(butyltelluro) thiophene as a convenient precursor for the synthesis of 2,5-bis-(acetylenic) thiophenes. Tetrahedron Letters, 44( 4), 685-688. doi:10.1016/s0040-4039(02)02659-x
    • NLM

      Zeni G, Zeni G, Nogueira CW, Silva DO, Menezes PH, Braga AL, Stefani HA, Rocha JBT. 2,5-Bis-(butyltelluro) thiophene as a convenient precursor for the synthesis of 2,5-bis-(acetylenic) thiophenes [Internet]. Tetrahedron Letters. 2003 ; 44( 4): 685-688.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4039(02)02659-x
    • Vancouver

      Zeni G, Zeni G, Nogueira CW, Silva DO, Menezes PH, Braga AL, Stefani HA, Rocha JBT. 2,5-Bis-(butyltelluro) thiophene as a convenient precursor for the synthesis of 2,5-bis-(acetylenic) thiophenes [Internet]. Tetrahedron Letters. 2003 ; 44( 4): 685-688.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4039(02)02659-x
  • Source: Tetrahedron. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, SESQUITERPENOS

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      FERRAZ, Helena Maria Carvalho e AGUILAR, Andrea Maria e SILVA JR., Luiz Fernando da. A diastereoselective total synthesis of the sesquiterpene (+or-)-mutisianthol. Tetrahedron, v. 59, n. 31, p. 5817-5821, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(03)00974-8. Acesso em: 02 out. 2024.
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      Ferraz, H. M. C., Aguilar, A. M., & Silva Jr., L. F. da. (2003). A diastereoselective total synthesis of the sesquiterpene (+or-)-mutisianthol. Tetrahedron, 59( 31), 5817-5821. doi:10.1016/s0040-4020(03)00974-8
    • NLM

      Ferraz HMC, Aguilar AM, Silva Jr. LF da. A diastereoselective total synthesis of the sesquiterpene (+or-)-mutisianthol [Internet]. Tetrahedron. 2003 ; 59( 31): 5817-5821.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(03)00974-8
    • Vancouver

      Ferraz HMC, Aguilar AM, Silva Jr. LF da. A diastereoselective total synthesis of the sesquiterpene (+or-)-mutisianthol [Internet]. Tetrahedron. 2003 ; 59( 31): 5817-5821.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(03)00974-8
  • Source: Journal of Organie Chemistry. Unidade: FFCLRP

    Assunto: SÍNTESE ORGÂNICA

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      FREDERICO, Daniel et al. A short and efficient synthesis of crocetin-dimethylester and crocetindial. Journal of Organie Chemistry, v. 68, p. 9126-9128, 2003Tradução . . Acesso em: 02 out. 2024.
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      Frederico, D., Donate, P. M., Constantino, M. G., Bronze, É. S., & Sairre, M. I. (2003). A short and efficient synthesis of crocetin-dimethylester and crocetindial. Journal of Organie Chemistry, 68, 9126-9128.
    • NLM

      Frederico D, Donate PM, Constantino MG, Bronze ÉS, Sairre MI. A short and efficient synthesis of crocetin-dimethylester and crocetindial. Journal of Organie Chemistry. 2003 ; 68 9126-9128.[citado 2024 out. 02 ]
    • Vancouver

      Frederico D, Donate PM, Constantino MG, Bronze ÉS, Sairre MI. A short and efficient synthesis of crocetin-dimethylester and crocetindial. Journal of Organie Chemistry. 2003 ; 68 9126-9128.[citado 2024 out. 02 ]
  • Source: Bioorganic e Medicinal Chemistry Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, BIOQUÍMICA ORGÂNICA, VENENOS DE ORIGEM ANIMAL, ARANHAS

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      NIHEI, Ken-ichi et al. An efficient and versatile synthesis of acylpolyamine spider toxins. Bioorganic e Medicinal Chemistry Letters, v. 12, n. 3, p. 299-302, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0960-894x(01)00733-8. Acesso em: 02 out. 2024.
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      Nihei, K. -ichi, Kato, M. J., Palma, M. S., & Konno, katsuhiro. (2002). An efficient and versatile synthesis of acylpolyamine spider toxins. Bioorganic e Medicinal Chemistry Letters, 12( 3), 299-302. doi:10.1016/s0960-894x(01)00733-8
    • NLM

      Nihei K-ichi, Kato MJ, Palma MS, Konno katsuhiro. An efficient and versatile synthesis of acylpolyamine spider toxins [Internet]. Bioorganic e Medicinal Chemistry Letters. 2002 ; 12( 3): 299-302.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0960-894x(01)00733-8
    • Vancouver

      Nihei K-ichi, Kato MJ, Palma MS, Konno katsuhiro. An efficient and versatile synthesis of acylpolyamine spider toxins [Internet]. Bioorganic e Medicinal Chemistry Letters. 2002 ; 12( 3): 299-302.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0960-894x(01)00733-8
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, TELÚRIO, COMPOSTOS DE OXIGÊNIO

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      ZINN, Fabiano K. et al. 'beta'-functionalized selenides and tellurides by hydrochalcogenation of olefins containing electron-withdrawing groups. Tetrahedron Letters, v. 43, n. 9, p. 1625-1628, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0040-4039(02)00095-3. Acesso em: 02 out. 2024.
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      Zinn, F. K., Righi, V. E., Luque, S. C., Formiga, H. B., & Comasseto, J. V. (2002). 'beta'-functionalized selenides and tellurides by hydrochalcogenation of olefins containing electron-withdrawing groups. Tetrahedron Letters, 43( 9), 1625-1628. doi:10.1016/s0040-4039(02)00095-3
    • NLM

      Zinn FK, Righi VE, Luque SC, Formiga HB, Comasseto JV. 'beta'-functionalized selenides and tellurides by hydrochalcogenation of olefins containing electron-withdrawing groups [Internet]. Tetrahedron Letters. 2002 ; 43( 9): 1625-1628.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4039(02)00095-3
    • Vancouver

      Zinn FK, Righi VE, Luque SC, Formiga HB, Comasseto JV. 'beta'-functionalized selenides and tellurides by hydrochalcogenation of olefins containing electron-withdrawing groups [Internet]. Tetrahedron Letters. 2002 ; 43( 9): 1625-1628.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4039(02)00095-3
  • Source: Acta Crystallographica Sction C - Crystal Strucuture Communications. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, CRISTALOGRAFIA ESTRUTURAL, SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS, ESTEREOQUÍMICA

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      ZUKERMAN-SCHPECTOR, Júlio et al. Two intermediates in the synthesis of decahydroisoquinolines with NMDA and AMPA receptor antagonist activity. Acta Crystallographica Sction C - Crystal Strucuture Communications, v. 57, p. 1089-1091, 2001Tradução . . Disponível em: https://doi.org/10.1107/s0108270101009702. Acesso em: 02 out. 2024.
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      Zukerman-Schpector, J., Vega, M., Caracelli, I., Dias, L. C., & Fernandes, A. M. A. P. (2001). Two intermediates in the synthesis of decahydroisoquinolines with NMDA and AMPA receptor antagonist activity. Acta Crystallographica Sction C - Crystal Strucuture Communications, 57, 1089-1091. doi:10.1107/s0108270101009702
    • NLM

      Zukerman-Schpector J, Vega M, Caracelli I, Dias LC, Fernandes AMAP. Two intermediates in the synthesis of decahydroisoquinolines with NMDA and AMPA receptor antagonist activity [Internet]. Acta Crystallographica Sction C - Crystal Strucuture Communications. 2001 ; 57 1089-1091.[citado 2024 out. 02 ] Available from: https://doi.org/10.1107/s0108270101009702
    • Vancouver

      Zukerman-Schpector J, Vega M, Caracelli I, Dias LC, Fernandes AMAP. Two intermediates in the synthesis of decahydroisoquinolines with NMDA and AMPA receptor antagonist activity [Internet]. Acta Crystallographica Sction C - Crystal Strucuture Communications. 2001 ; 57 1089-1091.[citado 2024 out. 02 ] Available from: https://doi.org/10.1107/s0108270101009702
  • Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, REAÇÕES ORGÂNICAS, SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS, COMPOSTOS ORGANOMETÁLICOS, TÁLIO

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      FERRAZ, Helena Maria Carvalho e SILVA JR., Luiz Fernando da. Construction of functionalized indans by thallium(III) promoted ring contraction of 3-alkenols. Tetrahedron, v. 57, n. 50, p. 9939-9949, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(01)01021-3. Acesso em: 02 out. 2024.
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      Ferraz, H. M. C., & Silva Jr., L. F. da. (2001). Construction of functionalized indans by thallium(III) promoted ring contraction of 3-alkenols. Tetrahedron, 57( 50), 9939-9949. doi:10.1016/s0040-4020(01)01021-3
    • NLM

      Ferraz HMC, Silva Jr. LF da. Construction of functionalized indans by thallium(III) promoted ring contraction of 3-alkenols [Internet]. Tetrahedron. 2001 ; 57( 50): 9939-9949.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(01)01021-3
    • Vancouver

      Ferraz HMC, Silva Jr. LF da. Construction of functionalized indans by thallium(III) promoted ring contraction of 3-alkenols [Internet]. Tetrahedron. 2001 ; 57( 50): 9939-9949.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(01)01021-3

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