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  • Fonte: Tetrahedron. Unidade: FFCLRP

    Assuntos: TERAPIA FOTODINÂMICA, QUÍMICA

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    • ABNT

      OLIVEIRA, Kleber T. et al. Synthesis of new amphiphilic chlorin derivaties from protoporphyrin-x dimethyl ester. Tetrahedron, v. 64, n. 37, p. 8709-8715, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.06.103. Acesso em: 02 out. 2024.
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      Oliveira, K. T., Silva, A. M. S., Tomé, A. C., Neves, M. G. P. M. S., Neri, C. R., Garcia, V. S., et al. (2008). Synthesis of new amphiphilic chlorin derivaties from protoporphyrin-x dimethyl ester. Tetrahedron, 64( 37), 8709-8715. doi:10.1016/j.tet.2008.06.103
    • NLM

      Oliveira KT, Silva AMS, Tomé AC, Neves MGPMS, Neri CR, Garcia VS, Serra OA, Iamamoto Y, Cavaleiro JAS. Synthesis of new amphiphilic chlorin derivaties from protoporphyrin-x dimethyl ester [Internet]. Tetrahedron. 2008 ; 64( 37): 8709-8715.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tet.2008.06.103
    • Vancouver

      Oliveira KT, Silva AMS, Tomé AC, Neves MGPMS, Neri CR, Garcia VS, Serra OA, Iamamoto Y, Cavaleiro JAS. Synthesis of new amphiphilic chlorin derivaties from protoporphyrin-x dimethyl ester [Internet]. Tetrahedron. 2008 ; 64( 37): 8709-8715.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tet.2008.06.103
  • Fonte: Tetrahedron. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      SILVA, Gil Valdo José da e CUNHA NETO, Álvaro. Calculated NMR as a tool for structural elucidation of jungianol and mutisianthol. Tetrahedron, v. 61, p. 7763-7767, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2005.05.101. Acesso em: 02 out. 2024.
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      Silva, G. V. J. da, & Cunha Neto, Á. (2005). Calculated NMR as a tool for structural elucidation of jungianol and mutisianthol. Tetrahedron, 61, 7763-7767. doi:10.1016/j.tet.2005.05.101
    • NLM

      Silva GVJ da, Cunha Neto Á. Calculated NMR as a tool for structural elucidation of jungianol and mutisianthol [Internet]. Tetrahedron. 2005 ; 61 7763-7767.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tet.2005.05.101
    • Vancouver

      Silva GVJ da, Cunha Neto Á. Calculated NMR as a tool for structural elucidation of jungianol and mutisianthol [Internet]. Tetrahedron. 2005 ; 61 7763-7767.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tet.2005.05.101
  • Fonte: Tetrahedron. Unidades: FFCLRP, FCFRP

    Assunto: FÁRMACOS (QUÍMICA)

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    • ABNT

      DONATE, Paulo Marcos et al. Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides. Tetrahedron, v. 14, p. 3253-3256, 2003Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2003.08.031. Acesso em: 02 out. 2024.
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      Donate, P. M., Frederico, D., Silva, R. da, Constantino, M. G., Del Ponte, G., & Bonatto, P. S. (2003). Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides. Tetrahedron, 14, 3253-3256. doi:10.1016/j.tetasy.2003.08.031
    • NLM

      Donate PM, Frederico D, Silva R da, Constantino MG, Del Ponte G, Bonatto PS. Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides [Internet]. Tetrahedron. 2003 ; 14 3253-3256.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetasy.2003.08.031
    • Vancouver

      Donate PM, Frederico D, Silva R da, Constantino MG, Del Ponte G, Bonatto PS. Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides [Internet]. Tetrahedron. 2003 ; 14 3253-3256.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tetasy.2003.08.031
  • Fonte: Tetrahedron. Unidades: FFCLRP, FCFRP

    Assunto: SÍNTESE QUÍMICA

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    • ABNT

      DABDOUB, Miguel Joaquim et al. Synthesis of (Z)-1-phenylseleno-1,4-diorganyl-1-buten-3-ynes: hydroselenation of symmetrical and usymmetrical 1,4-diorganyl-1, 3-butadiynes. Tetrahedron, v. 57, p. 4271-4276, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(01)00337-4. Acesso em: 02 out. 2024.
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      Dabdoub, M. J., Baroni, A. C., Lenardão, É. J., Gianeti, T. R., & Hurtado, G. R. (2001). Synthesis of (Z)-1-phenylseleno-1,4-diorganyl-1-buten-3-ynes: hydroselenation of symmetrical and usymmetrical 1,4-diorganyl-1, 3-butadiynes. Tetrahedron, 57, 4271-4276. doi:10.1016/s0040-4020(01)00337-4
    • NLM

      Dabdoub MJ, Baroni AC, Lenardão ÉJ, Gianeti TR, Hurtado GR. Synthesis of (Z)-1-phenylseleno-1,4-diorganyl-1-buten-3-ynes: hydroselenation of symmetrical and usymmetrical 1,4-diorganyl-1, 3-butadiynes [Internet]. Tetrahedron. 2001 ; 57 4271-4276.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(01)00337-4
    • Vancouver

      Dabdoub MJ, Baroni AC, Lenardão ÉJ, Gianeti TR, Hurtado GR. Synthesis of (Z)-1-phenylseleno-1,4-diorganyl-1-buten-3-ynes: hydroselenation of symmetrical and usymmetrical 1,4-diorganyl-1, 3-butadiynes [Internet]. Tetrahedron. 2001 ; 57 4271-4276.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(01)00337-4
  • Fonte: Tetrahedron. Unidade: FFCLRP

    Assuntos: SÍNDROME DE IMUNODEFICIÊNCIA ADQUIRIDA (QUIMIOTERAPIA), INIBIDORES QUÍMICOS

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    • ABNT

      PARREIRA, Renato L. T. e ABRAHÃO JÚNIOR, Odonírio e GALEMBECK, Sérgio Emanuel. Conformational preferences of non-nucleoside HIV-1 reverse transcriptase inhibitors. Tetrahedron, v. 57, p. 3243-3253, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(01)00193-4. Acesso em: 02 out. 2024.
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      Parreira, R. L. T., Abrahão Júnior, O., & Galembeck, S. E. (2001). Conformational preferences of non-nucleoside HIV-1 reverse transcriptase inhibitors. Tetrahedron, 57, 3243-3253. doi:10.1016/s0040-4020(01)00193-4
    • NLM

      Parreira RLT, Abrahão Júnior O, Galembeck SE. Conformational preferences of non-nucleoside HIV-1 reverse transcriptase inhibitors [Internet]. Tetrahedron. 2001 ; 57 3243-3253.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(01)00193-4
    • Vancouver

      Parreira RLT, Abrahão Júnior O, Galembeck SE. Conformational preferences of non-nucleoside HIV-1 reverse transcriptase inhibitors [Internet]. Tetrahedron. 2001 ; 57 3243-3253.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(01)00193-4
  • Fonte: Tetrahedron. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      SILVEIRA, Claudio da Cruz et al. Phenyltelluroacrylonitriles and phenylselenoacrylonitriles as precursors of (Z)-'alfa'-phenylseleno-'alfa','beta'-unsaturated aldehydes, 'beta'-amino-'alfa'-phenylselenonitriles and diels-alder adducts. Tetrahedron, v. 57, p. 5953-5959, 2001Tradução . . Disponível em: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v57i0028&article=5953_papapoaada&form=pdf&file=file.pdf. Acesso em: 02 out. 2024.
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      Silveira, C. da C., Perin, G., Braga, A. L., Dabdoub, M. J., & Jacob, R. G. (2001). Phenyltelluroacrylonitriles and phenylselenoacrylonitriles as precursors of (Z)-'alfa'-phenylseleno-'alfa','beta'-unsaturated aldehydes, 'beta'-amino-'alfa'-phenylselenonitriles and diels-alder adducts. Tetrahedron, 57, 5953-5959. Recuperado de http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v57i0028&article=5953_papapoaada&form=pdf&file=file.pdf
    • NLM

      Silveira C da C, Perin G, Braga AL, Dabdoub MJ, Jacob RG. Phenyltelluroacrylonitriles and phenylselenoacrylonitriles as precursors of (Z)-'alfa'-phenylseleno-'alfa','beta'-unsaturated aldehydes, 'beta'-amino-'alfa'-phenylselenonitriles and diels-alder adducts [Internet]. Tetrahedron. 2001 ; 57 5953-5959.[citado 2024 out. 02 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v57i0028&article=5953_papapoaada&form=pdf&file=file.pdf
    • Vancouver

      Silveira C da C, Perin G, Braga AL, Dabdoub MJ, Jacob RG. Phenyltelluroacrylonitriles and phenylselenoacrylonitriles as precursors of (Z)-'alfa'-phenylseleno-'alfa','beta'-unsaturated aldehydes, 'beta'-amino-'alfa'-phenylselenonitriles and diels-alder adducts [Internet]. Tetrahedron. 2001 ; 57 5953-5959.[citado 2024 out. 02 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v57i0028&article=5953_papapoaada&form=pdf&file=file.pdf
  • Fonte: Tetrahedron. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      ARMELIN, Elaine Aparecida e DONATE, Paulo Marcos e GALEMBECK, Sérgio Emanuel. Effect of the environment on the reactivity of 4'-substituted flavones and isoflavones. Tetrahedron, v. 56, p. 5105-5111, 2000Tradução . . Disponível em: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v56i0029&article=5105_eoteotro4fai&form=pdf&file=file.pdf. Acesso em: 02 out. 2024.
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      Armelin, E. A., Donate, P. M., & Galembeck, S. E. (2000). Effect of the environment on the reactivity of 4'-substituted flavones and isoflavones. Tetrahedron, 56, 5105-5111. Recuperado de http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v56i0029&article=5105_eoteotro4fai&form=pdf&file=file.pdf
    • NLM

      Armelin EA, Donate PM, Galembeck SE. Effect of the environment on the reactivity of 4'-substituted flavones and isoflavones [Internet]. Tetrahedron. 2000 ; 56 5105-5111.[citado 2024 out. 02 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v56i0029&article=5105_eoteotro4fai&form=pdf&file=file.pdf
    • Vancouver

      Armelin EA, Donate PM, Galembeck SE. Effect of the environment on the reactivity of 4'-substituted flavones and isoflavones [Internet]. Tetrahedron. 2000 ; 56 5105-5111.[citado 2024 out. 02 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v56i0029&article=5105_eoteotro4fai&form=pdf&file=file.pdf
  • Fonte: Tetrahedron. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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      NAMBA, Adriana Mieco et al. Dynamics of p-menthan-3,9-diols. A computational study in aqueous and chloroform solutions of two epimers. Tetrahedron, v. 56, p. 6089-6097, 2000Tradução . . Disponível em: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v56i0033&article=6089_dopacsacsote&form=pdf&file=file.pdf. Acesso em: 02 out. 2024.
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      Namba, A. M., León, S., Silva, G. V. J. da, & Alemán, C. (2000). Dynamics of p-menthan-3,9-diols. A computational study in aqueous and chloroform solutions of two epimers. Tetrahedron, 56, 6089-6097. Recuperado de http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v56i0033&article=6089_dopacsacsote&form=pdf&file=file.pdf
    • NLM

      Namba AM, León S, Silva GVJ da, Alemán C. Dynamics of p-menthan-3,9-diols. A computational study in aqueous and chloroform solutions of two epimers [Internet]. Tetrahedron. 2000 ; 56 6089-6097.[citado 2024 out. 02 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v56i0033&article=6089_dopacsacsote&form=pdf&file=file.pdf
    • Vancouver

      Namba AM, León S, Silva GVJ da, Alemán C. Dynamics of p-menthan-3,9-diols. A computational study in aqueous and chloroform solutions of two epimers [Internet]. Tetrahedron. 2000 ; 56 6089-6097.[citado 2024 out. 02 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v56i0033&article=6089_dopacsacsote&form=pdf&file=file.pdf
  • Fonte: Tetrahedron. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      DABDOUB, Miguel Joaquim e BEGNINI, Mauro L e GUERREDRO JUNIOR, G. Hydrozirconation of acetylenic chalcogenides: synthesis and reactions of zirconated vinyl chalcogenide intermediates. Tetrahedron, v. 54, p. 2371-2400, 1998Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(98)00014-3. Acesso em: 02 out. 2024.
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      Dabdoub, M. J., Begnini, M. L., & Guerredro Junior, G. (1998). Hydrozirconation of acetylenic chalcogenides: synthesis and reactions of zirconated vinyl chalcogenide intermediates. Tetrahedron, 54, 2371-2400. doi:10.1016/s0040-4020(98)00014-3
    • NLM

      Dabdoub MJ, Begnini ML, Guerredro Junior G. Hydrozirconation of acetylenic chalcogenides: synthesis and reactions of zirconated vinyl chalcogenide intermediates [Internet]. Tetrahedron. 1998 ; 54 2371-2400.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(98)00014-3
    • Vancouver

      Dabdoub MJ, Begnini ML, Guerredro Junior G. Hydrozirconation of acetylenic chalcogenides: synthesis and reactions of zirconated vinyl chalcogenide intermediates [Internet]. Tetrahedron. 1998 ; 54 2371-2400.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(98)00014-3
  • Fonte: Tetrahedron. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      CONSTANTINO, Maurício Gomes e SILVA, Gil Valdo José da. Stereochemistry in substituted cyclopentanes: an approach to the analysis by proton NMR. Tetrahedron, v. 54, p. 11363-11274, 1998Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(98)00630-9. Acesso em: 02 out. 2024.
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      Constantino, M. G., & Silva, G. V. J. da. (1998). Stereochemistry in substituted cyclopentanes: an approach to the analysis by proton NMR. Tetrahedron, 54, 11363-11274. doi:10.1016/s0040-4020(98)00630-9
    • NLM

      Constantino MG, Silva GVJ da. Stereochemistry in substituted cyclopentanes: an approach to the analysis by proton NMR [Internet]. Tetrahedron. 1998 ; 54 11363-11274.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(98)00630-9
    • Vancouver

      Constantino MG, Silva GVJ da. Stereochemistry in substituted cyclopentanes: an approach to the analysis by proton NMR [Internet]. Tetrahedron. 1998 ; 54 11363-11274.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(98)00630-9
  • Fonte: Tetrahedron. Unidade: FFCLRP

    Assunto: QUÍMICA

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    • ABNT

      DABDOUB, Miguel Joaquim et al. (1z,3z)-buta-1,3-dienyl-1-lithium species and substituted tellurophenes by te/li exchange on (1z,3z)-butyltelluro-1,3-butadienes and (1z,3z)-1,4-bis(butyltelluro)-1,3-butadienes. Tetrahedron, v. 53, n. 12, p. 4199-4218, 1997Tradução . . Acesso em: 02 out. 2024.
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      Dabdoub, M. J., Dabdoub, V. B., Guerrero Junior, P. G., & Silveira, C. C. (1997). (1z,3z)-buta-1,3-dienyl-1-lithium species and substituted tellurophenes by te/li exchange on (1z,3z)-butyltelluro-1,3-butadienes and (1z,3z)-1,4-bis(butyltelluro)-1,3-butadienes. Tetrahedron, 53( 12), 4199-4218.
    • NLM

      Dabdoub MJ, Dabdoub VB, Guerrero Junior PG, Silveira CC. (1z,3z)-buta-1,3-dienyl-1-lithium species and substituted tellurophenes by te/li exchange on (1z,3z)-butyltelluro-1,3-butadienes and (1z,3z)-1,4-bis(butyltelluro)-1,3-butadienes. Tetrahedron. 1997 ; 53( 12): 4199-4218.[citado 2024 out. 02 ]
    • Vancouver

      Dabdoub MJ, Dabdoub VB, Guerrero Junior PG, Silveira CC. (1z,3z)-buta-1,3-dienyl-1-lithium species and substituted tellurophenes by te/li exchange on (1z,3z)-butyltelluro-1,3-butadienes and (1z,3z)-1,4-bis(butyltelluro)-1,3-butadienes. Tetrahedron. 1997 ; 53( 12): 4199-4218.[citado 2024 out. 02 ]
  • Fonte: Tetrahedron. Unidade: FFCLRP

    Assunto: QUÍMICA

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      DABDOUB, Miguel Joaquim e DABDOUB, V B. Highly chemoselective triple bond reductions on unsymmetrical 1,4-diorganyl-1,3-butadiynes. Tetrahedron, v. 51, n. 36, p. 9839-50, 1996Tradução . . Disponível em: https://doi.org/10.1016/0040-4020(95)00564-o. Acesso em: 02 out. 2024.
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      Dabdoub, M. J., & Dabdoub, V. B. (1996). Highly chemoselective triple bond reductions on unsymmetrical 1,4-diorganyl-1,3-butadiynes. Tetrahedron, 51( 36), 9839-50. doi:10.1016/0040-4020(95)00564-o
    • NLM

      Dabdoub MJ, Dabdoub VB. Highly chemoselective triple bond reductions on unsymmetrical 1,4-diorganyl-1,3-butadiynes [Internet]. Tetrahedron. 1996 ;51( 36): 9839-50.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/0040-4020(95)00564-o
    • Vancouver

      Dabdoub MJ, Dabdoub VB. Highly chemoselective triple bond reductions on unsymmetrical 1,4-diorganyl-1,3-butadiynes [Internet]. Tetrahedron. 1996 ;51( 36): 9839-50.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/0040-4020(95)00564-o
  • Fonte: Tetrahedron. Unidade: FFCLRP

    Assunto: QUÍMICA

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      DABDOUB, Miguel Joaquim e CASSOL, T M. Total control on the synthesis of regio and stereoisomers . Of vinylic tellurides. Tetrahedron, v. 51, n. 47, p. 12971-82, 1995Tradução . . Disponível em: https://doi.org/10.1016/0040-4020(95)00840-5. Acesso em: 02 out. 2024.
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      Dabdoub, M. J., & Cassol, T. M. (1995). Total control on the synthesis of regio and stereoisomers . Of vinylic tellurides. Tetrahedron, 51( 47), 12971-82. doi:10.1016/0040-4020(95)00840-5
    • NLM

      Dabdoub MJ, Cassol TM. Total control on the synthesis of regio and stereoisomers . Of vinylic tellurides [Internet]. Tetrahedron. 1995 ;51( 47): 12971-82.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/0040-4020(95)00840-5
    • Vancouver

      Dabdoub MJ, Cassol TM. Total control on the synthesis of regio and stereoisomers . Of vinylic tellurides [Internet]. Tetrahedron. 1995 ;51( 47): 12971-82.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/0040-4020(95)00840-5
  • Fonte: Tetrahedron. Unidades: FFCLRP, FCFRP

    Assunto: QUÍMICA

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      TEDESCO, A C et al. Kinetic studies of the nucleophilic quenching of photoexcited nitroanyl ethers (n'AR'e) by bromide ions in cationia micellar solution. Tetrahedron, v. 50, p. 3071-80, 1994Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(01)81107-8. Acesso em: 02 out. 2024.
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      Tedesco, A. C., Naal, R. M. Z. G., Carreiro, J. C., & Bonilha, J. B. S. (1994). Kinetic studies of the nucleophilic quenching of photoexcited nitroanyl ethers (n'AR'e) by bromide ions in cationia micellar solution. Tetrahedron, 50, 3071-80. doi:10.1016/s0040-4020(01)81107-8
    • NLM

      Tedesco AC, Naal RMZG, Carreiro JC, Bonilha JBS. Kinetic studies of the nucleophilic quenching of photoexcited nitroanyl ethers (n'AR'e) by bromide ions in cationia micellar solution [Internet]. Tetrahedron. 1994 ;50 3071-80.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(01)81107-8
    • Vancouver

      Tedesco AC, Naal RMZG, Carreiro JC, Bonilha JBS. Kinetic studies of the nucleophilic quenching of photoexcited nitroanyl ethers (n'AR'e) by bromide ions in cationia micellar solution [Internet]. Tetrahedron. 1994 ;50 3071-80.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(01)81107-8
  • Fonte: Tetrahedron. Unidades: IP, FFCLRP

    Assunto: QUÍMICA

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    • ABNT

      BONILHA, J B S et al. Further evidence for the triplet mechanism in the photosubstitution of nitroanyl ethers in alkaline medium. Tetrahedron, v. 49, n. 15, p. 3053-64, 1993Tradução . . Acesso em: 02 out. 2024.
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      Bonilha, J. B. S., Tedesco, A. C., Nogueira, L. C., Diamantino, M. T. R. S., & Carreiro, J. C. (1993). Further evidence for the triplet mechanism in the photosubstitution of nitroanyl ethers in alkaline medium. Tetrahedron, 49( 15), 3053-64.
    • NLM

      Bonilha JBS, Tedesco AC, Nogueira LC, Diamantino MTRS, Carreiro JC. Further evidence for the triplet mechanism in the photosubstitution of nitroanyl ethers in alkaline medium. Tetrahedron. 1993 ;49( 15): 3053-64.[citado 2024 out. 02 ]
    • Vancouver

      Bonilha JBS, Tedesco AC, Nogueira LC, Diamantino MTRS, Carreiro JC. Further evidence for the triplet mechanism in the photosubstitution of nitroanyl ethers in alkaline medium. Tetrahedron. 1993 ;49( 15): 3053-64.[citado 2024 out. 02 ]
  • Fonte: Tetrahedron. Unidade: FFCLRP

    Assunto: QUÍMICA

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    • ABNT

      NAVARRO, M e DE GIOVANI, Wagner Ferraresi e ROMERO, José Ricardo. Selectivity in catalytic diol electrooxidation using a polypyridine 'RU' (iv) complex. Tetrahedron, v. 47, p. 851, 1991Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(01)87073-3. Acesso em: 02 out. 2024.
    • APA

      Navarro, M., De Giovani, W. F., & Romero, J. R. (1991). Selectivity in catalytic diol electrooxidation using a polypyridine 'RU' (iv) complex. Tetrahedron, 47, 851. doi:10.1016/s0040-4020(01)87073-3
    • NLM

      Navarro M, De Giovani WF, Romero JR. Selectivity in catalytic diol electrooxidation using a polypyridine 'RU' (iv) complex [Internet]. Tetrahedron. 1991 ;47 851.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(01)87073-3
    • Vancouver

      Navarro M, De Giovani WF, Romero JR. Selectivity in catalytic diol electrooxidation using a polypyridine 'RU' (iv) complex [Internet]. Tetrahedron. 1991 ;47 851.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/s0040-4020(01)87073-3

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