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  • Source: Synthesis. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, TÁLIO, NITRATOS, CARBONO

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      FERRAZ, Helena Maria Carvalho e CARNEIRO, Vânia Maria Teixeira e SILVA JUNIOR, Luiz Fernando da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes. Synthesis, n. 3, p. 385-388, 2009Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf. Acesso em: 18 out. 2024.
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      Ferraz, H. M. C., Carneiro, V. M. T., & Silva Junior, L. F. da. (2009). Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes. Synthesis, ( 3), 385-388. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
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      Ferraz HMC, Carneiro VMT, Silva Junior LF da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes [Internet]. Synthesis. 2009 ;( 3): 385-388.[citado 2024 out. 18 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
    • Vancouver

      Ferraz HMC, Carneiro VMT, Silva Junior LF da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes [Internet]. Synthesis. 2009 ;( 3): 385-388.[citado 2024 out. 18 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
  • Source: Journal of Inclusion Phenomena and Macrocyclic Chemistry. Unidade: IQ

    Subjects: ANTIOXIDANTES, METABÓLITOS SECUNDÁRIOS

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      SOARES, Lílian Amélia et al. Host-guest system of 4-nerolidylcatechol in 2-hydroxypropyl 'beta'-cyclodextrin: preparation, characterization and molecular modeling. Journal of Inclusion Phenomena and Macrocyclic Chemistry, v. 64, n. 1-2, p. 23-35, 2009Tradução . . Disponível em: http://www.springerlink.com.w10077.dotlib.com.br/content/ku4h8574977u25g1/fulltext.pdf. Acesso em: 18 out. 2024.
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      Soares, L. A., Leal, A. F. V. B., Fraceto, L. F., Maia, E. R., Resck, I. S., Kato, M. J., et al. (2009). Host-guest system of 4-nerolidylcatechol in 2-hydroxypropyl 'beta'-cyclodextrin: preparation, characterization and molecular modeling. Journal of Inclusion Phenomena and Macrocyclic Chemistry, 64( 1-2), 23-35. Recuperado de http://www.springerlink.com.w10077.dotlib.com.br/content/ku4h8574977u25g1/fulltext.pdf
    • NLM

      Soares LA, Leal AFVB, Fraceto LF, Maia ER, Resck IS, Kato MJ, Gil E de S, Sousa AR de, Cunha LC da, Rezende KR. Host-guest system of 4-nerolidylcatechol in 2-hydroxypropyl 'beta'-cyclodextrin: preparation, characterization and molecular modeling [Internet]. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2009 ; 64( 1-2): 23-35.[citado 2024 out. 18 ] Available from: http://www.springerlink.com.w10077.dotlib.com.br/content/ku4h8574977u25g1/fulltext.pdf
    • Vancouver

      Soares LA, Leal AFVB, Fraceto LF, Maia ER, Resck IS, Kato MJ, Gil E de S, Sousa AR de, Cunha LC da, Rezende KR. Host-guest system of 4-nerolidylcatechol in 2-hydroxypropyl 'beta'-cyclodextrin: preparation, characterization and molecular modeling [Internet]. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2009 ; 64( 1-2): 23-35.[citado 2024 out. 18 ] Available from: http://www.springerlink.com.w10077.dotlib.com.br/content/ku4h8574977u25g1/fulltext.pdf
  • Source: Synlett. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, PALÁDIO

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      SINGH, Fateh Veer e STEFANI, Hélio Alexandre. Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed homocoupling of aryl n-butyl tellurides. Synlett, n. 20, p. 3221-3225, 2008Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf. Acesso em: 18 out. 2024.
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      Singh, F. V., & Stefani, H. A. (2008). Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed homocoupling of aryl n-butyl tellurides. Synlett, ( 20), 3221-3225. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf
    • NLM

      Singh FV, Stefani HA. Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed homocoupling of aryl n-butyl tellurides [Internet]. Synlett. 2008 ;( 20): 3221-3225.[citado 2024 out. 18 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf
    • Vancouver

      Singh FV, Stefani HA. Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed homocoupling of aryl n-butyl tellurides [Internet]. Synlett. 2008 ;( 20): 3221-3225.[citado 2024 out. 18 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf
  • Source: European Journal of Inorganic Chemistry. Unidades: FCFRP, IQ

    Subjects: VOLTAMETRIA, RUTÊNIO

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      NIKOLAOU, Sofia e TOMA, Henrique Eisi. A convergent approach for the generation of dendrimers containing the ['RU IND. 3'O'('CH IND. 3'COO) IND.6'] electroactive core. European Journal of Inorganic Chemistry, n. 14, p. 2266-2271, 2008Tradução . . Acesso em: 18 out. 2024.
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      Nikolaou, S., & Toma, H. E. (2008). A convergent approach for the generation of dendrimers containing the ['RU IND. 3'O'('CH IND. 3'COO) IND.6'] electroactive core. European Journal of Inorganic Chemistry, (14), 2266-2271.
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      Nikolaou S, Toma HE. A convergent approach for the generation of dendrimers containing the ['RU IND. 3'O'('CH IND. 3'COO) IND.6'] electroactive core. European Journal of Inorganic Chemistry. 2008 ;(14): 2266-2271.[citado 2024 out. 18 ]
    • Vancouver

      Nikolaou S, Toma HE. A convergent approach for the generation of dendrimers containing the ['RU IND. 3'O'('CH IND. 3'COO) IND.6'] electroactive core. European Journal of Inorganic Chemistry. 2008 ;(14): 2266-2271.[citado 2024 out. 18 ]
  • Source: European Journal of Organic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SOLVENTE

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      MARTINS, Clarissa Tavares et al. Thermo-solvatochromism of merocyanine polarity probes: What are the consequences of increasing probe lipophilicity through annelation?. European Journal of Organic Chemistry, n. 7, p. 1165-1180, 2008Tradução . . Acesso em: 18 out. 2024.
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      Martins, C. T., Lima, M. de S., Bastos, E. L., & El Seoud, O. A. (2008). Thermo-solvatochromism of merocyanine polarity probes: What are the consequences of increasing probe lipophilicity through annelation? European Journal of Organic Chemistry, (7), 1165-1180.
    • NLM

      Martins CT, Lima M de S, Bastos EL, El Seoud OA. Thermo-solvatochromism of merocyanine polarity probes: What are the consequences of increasing probe lipophilicity through annelation? European Journal of Organic Chemistry. 2008 ;(7): 1165-1180.[citado 2024 out. 18 ]
    • Vancouver

      Martins CT, Lima M de S, Bastos EL, El Seoud OA. Thermo-solvatochromism of merocyanine polarity probes: What are the consequences of increasing probe lipophilicity through annelation? European Journal of Organic Chemistry. 2008 ;(7): 1165-1180.[citado 2024 out. 18 ]
  • Source: Phosphorus, Sulfur, and Silicon and the Related Elements. Unidade: IQ

    Subjects: TELÚRIO, COMPOSTOS ORGANOMETÁLICOS, SÍNTESE ORGÂNICA

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      COMASSETO, João Valdir e DOS SANTOS, Alcindo Aparecido. Organotellurides as precursors of reactive organometallics. Phosphorus, Sulfur, and Silicon and the Related Elements, v. 183, n. 4, p. 939-947, 2008Tradução . . Acesso em: 18 out. 2024.
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      Comasseto, J. V., & Dos Santos, A. A. (2008). Organotellurides as precursors of reactive organometallics. Phosphorus, Sulfur, and Silicon and the Related Elements, 183( 4), 939-947.
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      Comasseto JV, Dos Santos AA. Organotellurides as precursors of reactive organometallics. Phosphorus, Sulfur, and Silicon and the Related Elements. 2008 ;183( 4): 939-947.[citado 2024 out. 18 ]
    • Vancouver

      Comasseto JV, Dos Santos AA. Organotellurides as precursors of reactive organometallics. Phosphorus, Sulfur, and Silicon and the Related Elements. 2008 ;183( 4): 939-947.[citado 2024 out. 18 ]
  • Source: Synthetic Communications. Unidade: IQ

    Subjects: LÍQUIDOS IÔNICOS, CATÁLISE, TELÚRIO

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      GARIANI, Rogério Aparecido e DOS SANTOS, Alcindo Aparecido e COMASSETO, João Valdir. In-situ generation of n-butanethiol and its reaction with electron-deficient olefins. Synthetic Communications, v. 38, n. 5, p. 789-795, 2008Tradução . . Acesso em: 18 out. 2024.
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      Gariani, R. A., Dos Santos, A. A., & Comasseto, J. V. (2008). In-situ generation of n-butanethiol and its reaction with electron-deficient olefins. Synthetic Communications, 38( 5), 789-795.
    • NLM

      Gariani RA, Dos Santos AA, Comasseto JV. In-situ generation of n-butanethiol and its reaction with electron-deficient olefins. Synthetic Communications. 2008 ; 38( 5): 789-795.[citado 2024 out. 18 ]
    • Vancouver

      Gariani RA, Dos Santos AA, Comasseto JV. In-situ generation of n-butanethiol and its reaction with electron-deficient olefins. Synthetic Communications. 2008 ; 38( 5): 789-795.[citado 2024 out. 18 ]
  • Source: European Journal of Inorganic Chemistry. Unidade: IQ

    Subjects: ESPECTROSCOPIA RAMAN, NANOPARTÍCULAS

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      TOMA, Sérgio Hiroshi et al. Controlled stabilization and flocculation of gold nanoparticles by means of 2-pyrazin-2-yiethanethiol and pentacyanidoferrate(II) complexes. European Journal of Inorganic Chemistry, n. 21, p. 3356-3364, 2007Tradução . . Acesso em: 18 out. 2024.
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      Toma, S. H., Bonacin, J. A., Araki, K., & Toma, H. E. (2007). Controlled stabilization and flocculation of gold nanoparticles by means of 2-pyrazin-2-yiethanethiol and pentacyanidoferrate(II) complexes. European Journal of Inorganic Chemistry, ( 21), 3356-3364.
    • NLM

      Toma SH, Bonacin JA, Araki K, Toma HE. Controlled stabilization and flocculation of gold nanoparticles by means of 2-pyrazin-2-yiethanethiol and pentacyanidoferrate(II) complexes. European Journal of Inorganic Chemistry. 2007 ;( 21): 3356-3364.[citado 2024 out. 18 ]
    • Vancouver

      Toma SH, Bonacin JA, Araki K, Toma HE. Controlled stabilization and flocculation of gold nanoparticles by means of 2-pyrazin-2-yiethanethiol and pentacyanidoferrate(II) complexes. European Journal of Inorganic Chemistry. 2007 ;( 21): 3356-3364.[citado 2024 out. 18 ]
  • Source: Journal of Mass Spectrometry. Unidade: IQ

    Subjects: ESPECTROSCOPIA DE MASSA, FÍSICO-QUÍMICA

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      FILETI, Eudes Eterno et al. Gas-phase electrophilic addition promoted by CH3S+= CH2 ions on aromatic systems. Journal of Mass Spectrometry, v. 42, n. 10, p. 1310-1318, 2007Tradução . . Disponível em: https://doi.org/10.1002/jms.1202. Acesso em: 18 out. 2024.
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      Fileti, E. E., Moraes, P. R. P., Domingues, L., & Riveros, J. M. (2007). Gas-phase electrophilic addition promoted by CH3S+= CH2 ions on aromatic systems. Journal of Mass Spectrometry, 42( 10), 1310-1318. doi:10.1002/jms.1202
    • NLM

      Fileti EE, Moraes PRP, Domingues L, Riveros JM. Gas-phase electrophilic addition promoted by CH3S+= CH2 ions on aromatic systems [Internet]. Journal of Mass Spectrometry. 2007 ;42( 10): 1310-1318.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/jms.1202
    • Vancouver

      Fileti EE, Moraes PRP, Domingues L, Riveros JM. Gas-phase electrophilic addition promoted by CH3S+= CH2 ions on aromatic systems [Internet]. Journal of Mass Spectrometry. 2007 ;42( 10): 1310-1318.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/jms.1202
  • Source: Synthesis. Unidade: IQ

    Subjects: TÁLIO, SÍNTESE ORGÂNICA

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      SILVA JUNIOR, Luiz Fernando da et al. Rearrangement of homoallylic alcohols with thallium(III): diastereoselective synthesis of Indans bearing a 'beta'-hydroxy ketone moiety. Synthesis, n. 3, p. 355-362, 2007Tradução . . Acesso em: 18 out. 2024.
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      Silva Junior, L. F. da, Quintiliano, S. A. P., Craveiro, M. V., Vieira, F. Y. M., & Ferraz, H. M. C. (2007). Rearrangement of homoallylic alcohols with thallium(III): diastereoselective synthesis of Indans bearing a 'beta'-hydroxy ketone moiety. Synthesis, ( 3), 355-362.
    • NLM

      Silva Junior LF da, Quintiliano SAP, Craveiro MV, Vieira FYM, Ferraz HMC. Rearrangement of homoallylic alcohols with thallium(III): diastereoselective synthesis of Indans bearing a 'beta'-hydroxy ketone moiety. Synthesis. 2007 ;( 3): 355-362.[citado 2024 out. 18 ]
    • Vancouver

      Silva Junior LF da, Quintiliano SAP, Craveiro MV, Vieira FYM, Ferraz HMC. Rearrangement of homoallylic alcohols with thallium(III): diastereoselective synthesis of Indans bearing a 'beta'-hydroxy ketone moiety. Synthesis. 2007 ;( 3): 355-362.[citado 2024 out. 18 ]
  • Source: European Journal of Inorganic Chemistry. Unidade: IQ

    Subjects: NIÓBIO, SOLUÇÕES AQUOSAS, MATERIAIS COMPÓSITOS

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      BIZETO, Marcos Augusto e CONSTANTINO, Vera Regina Leopoldo. Niobium oxide mesophases obtained by self-assembly of an aqueous soluble niobium complex precursor and organic templates. European Journal of Inorganic Chemistry, n. 4, p. 579-584, 2007Tradução . . Acesso em: 18 out. 2024.
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      Bizeto, M. A., & Constantino, V. R. L. (2007). Niobium oxide mesophases obtained by self-assembly of an aqueous soluble niobium complex precursor and organic templates. European Journal of Inorganic Chemistry, ( 4), 579-584.
    • NLM

      Bizeto MA, Constantino VRL. Niobium oxide mesophases obtained by self-assembly of an aqueous soluble niobium complex precursor and organic templates. European Journal of Inorganic Chemistry. 2007 ;( 4): 579-584.[citado 2024 out. 18 ]
    • Vancouver

      Bizeto MA, Constantino VRL. Niobium oxide mesophases obtained by self-assembly of an aqueous soluble niobium complex precursor and organic templates. European Journal of Inorganic Chemistry. 2007 ;( 4): 579-584.[citado 2024 out. 18 ]
  • Source: Journal of Inclusion Phenomena and Macrocyclic Chemistry. Unidade: FCF

    Subjects: ANESTÉSICOS LOCAIS, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, TERMODINÂMICA

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      MORAES, Carolina Morales et al. Characterization of lidocaine: hydroxypropyl-beta-cyclodextrin inclusion complex. Journal of Inclusion Phenomena and Macrocyclic Chemistry, v. 57, n. 1-4, p. 313-316, 2007Tradução . . Disponível em: https://doi.org/10.1007/s10847-006-9179-x. Acesso em: 18 out. 2024.
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      Moraes, C. M., Abrami, P., Araujo, D. R., Braga, A. de F. de A., Issa, M. G., Ferraz, H. G., et al. (2007). Characterization of lidocaine: hydroxypropyl-beta-cyclodextrin inclusion complex. Journal of Inclusion Phenomena and Macrocyclic Chemistry, 57( 1-4), 313-316. doi:10.1007/s10847-006-9179-x
    • NLM

      Moraes CM, Abrami P, Araujo DR, Braga A de F de A, Issa MG, Ferraz HG, Paula E de, Fraceto LF. Characterization of lidocaine: hydroxypropyl-beta-cyclodextrin inclusion complex [Internet]. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2007 ; 57( 1-4): 313-316.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/s10847-006-9179-x
    • Vancouver

      Moraes CM, Abrami P, Araujo DR, Braga A de F de A, Issa MG, Ferraz HG, Paula E de, Fraceto LF. Characterization of lidocaine: hydroxypropyl-beta-cyclodextrin inclusion complex [Internet]. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2007 ; 57( 1-4): 313-316.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/s10847-006-9179-x
  • Source: Macromolecular Rapid Communications. Unidade: IQ

    Subjects: ESPECTROSCOPIA RAMAN, NANOPARTÍCULAS

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      RODRIGUES, Fabio e DO NASCIMENTO, G. M. e SANTOS, Paulo Sérgio. Dissolution and doping of polyaniline emeraldine base in imidazolium ionic liquids investigated by spectroscopic techniques. Macromolecular Rapid Communications, v. 28, n. 5, p. 666-669, 2007Tradução . . Acesso em: 18 out. 2024.
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      Rodrigues, F., Do Nascimento, G. M., & Santos, P. S. (2007). Dissolution and doping of polyaniline emeraldine base in imidazolium ionic liquids investigated by spectroscopic techniques. Macromolecular Rapid Communications, 28( 5), 666-669.
    • NLM

      Rodrigues F, Do Nascimento GM, Santos PS. Dissolution and doping of polyaniline emeraldine base in imidazolium ionic liquids investigated by spectroscopic techniques. Macromolecular Rapid Communications. 2007 ; 28( 5): 666-669.[citado 2024 out. 18 ]
    • Vancouver

      Rodrigues F, Do Nascimento GM, Santos PS. Dissolution and doping of polyaniline emeraldine base in imidazolium ionic liquids investigated by spectroscopic techniques. Macromolecular Rapid Communications. 2007 ; 28( 5): 666-669.[citado 2024 out. 18 ]
  • Source: Synthesis. Unidade: IQ

    Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA

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      FERRAZ, Helena Maria Carvalho e BOMBONATO, Fernanda Irene e LONGO JUNIOR, Luiz Sidney. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis, n. 21, p. 3261-3285, 2007Tradução . . Acesso em: 18 out. 2024.
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      Ferraz, H. M. C., Bombonato, F. I., & Longo Junior, L. S. (2007). Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis, ( 21), 3261-3285.
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      Ferraz HMC, Bombonato FI, Longo Junior LS. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis. 2007 ;( 21): 3261-3285.[citado 2024 out. 18 ]
    • Vancouver

      Ferraz HMC, Bombonato FI, Longo Junior LS. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis. 2007 ;( 21): 3261-3285.[citado 2024 out. 18 ]
  • Source: European Journal of Inorganic Chemistry. Unidade: IQ

    Subjects: RUTÊNIO, ALDEÍDOS, ELETROQUÍMICA

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      NUNES, Genebaldo Sales et al. Proton-coupled redox chemistry, oxidative reactivity, and electronic characterization of aqua-, hydroxo-, and oxo-triruthenium clusters. European Journal of Inorganic Chemistry, n. 7, p. 1487-1495, 2006Tradução . . Acesso em: 18 out. 2024.
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      Nunes, G. S., Alexiou, A. D. P., Araki, K., Formiga, A. L. B., Rocha, R. C., & Toma, H. E. (2006). Proton-coupled redox chemistry, oxidative reactivity, and electronic characterization of aqua-, hydroxo-, and oxo-triruthenium clusters. European Journal of Inorganic Chemistry, ( 7), 1487-1495.
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      Nunes GS, Alexiou ADP, Araki K, Formiga ALB, Rocha RC, Toma HE. Proton-coupled redox chemistry, oxidative reactivity, and electronic characterization of aqua-, hydroxo-, and oxo-triruthenium clusters. European Journal of Inorganic Chemistry. 2006 ;( 7): 1487-1495.[citado 2024 out. 18 ]
    • Vancouver

      Nunes GS, Alexiou ADP, Araki K, Formiga ALB, Rocha RC, Toma HE. Proton-coupled redox chemistry, oxidative reactivity, and electronic characterization of aqua-, hydroxo-, and oxo-triruthenium clusters. European Journal of Inorganic Chemistry. 2006 ;( 7): 1487-1495.[citado 2024 out. 18 ]
  • Source: Synthesis. Unidade: IQ

    Subjects: TÁLIO, QUÍMICA ORGÂNICA

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      FERRAZ, Helena Maria Carvalho e VIEIRA, Tiago O. e SILVA JR., Luiz Fernando da. Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis, n. 16, p. 2748-2752, 2006Tradução . . Acesso em: 18 out. 2024.
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      Ferraz, H. M. C., Vieira, T. O., & Silva Jr., L. F. da. (2006). Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis, ( 16), 2748-2752.
    • NLM

      Ferraz HMC, Vieira TO, Silva Jr. LF da. Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis. 2006 ;( 16): 2748-2752.[citado 2024 out. 18 ]
    • Vancouver

      Ferraz HMC, Vieira TO, Silva Jr. LF da. Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis. 2006 ;( 16): 2748-2752.[citado 2024 out. 18 ]
  • Source: Synthesis. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      BASTOS, Erick Leite et al. Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane]. Synthesis, n. 15, p. , 2006Tradução . . Disponível em: https://doi.org/10.1055/s-2006-942357. Acesso em: 18 out. 2024.
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      Bastos, E. L., Ciscato, L. F. M. L., Weiss, D., Beckert, R., & Baader, W. J. (2006). Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane]. Synthesis, ( 15), . doi:10.1055/s-2006-942357
    • NLM

      Bastos EL, Ciscato LFML, Weiss D, Beckert R, Baader WJ. Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane] [Internet]. Synthesis. 2006 ;( 15): .[citado 2024 out. 18 ] Available from: https://doi.org/10.1055/s-2006-942357
    • Vancouver

      Bastos EL, Ciscato LFML, Weiss D, Beckert R, Baader WJ. Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane] [Internet]. Synthesis. 2006 ;( 15): .[citado 2024 out. 18 ] Available from: https://doi.org/10.1055/s-2006-942357
  • Source: European Journal of Organic Chemistry. Unidade: IQ

    Subjects: LUMINESCÊNCIA, FOTOLUMINESCÊNCIA (SÍNTESE), ELETROQUÍMICA

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      MANCILHA, Fabiana Szczesny et al. Are molecular 5,8-pi-extended quinoxaline derivatives good chromophores for photoluminescence applications?. European Journal of Organic Chemistry, n. 21, p. 4924-4933, 2006Tradução . . Acesso em: 18 out. 2024.
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      Mancilha, F. S., DaSilveira Neto, B. A., Lopes, A. S. 'A., Moreira Júnior, P. F., Quina, F. H., Goncalves, R. S., & Dupont, J. (2006). Are molecular 5,8-pi-extended quinoxaline derivatives good chromophores for photoluminescence applications? European Journal of Organic Chemistry, ( 21), 4924-4933.
    • NLM

      Mancilha FS, DaSilveira Neto BA, Lopes AS'A, Moreira Júnior PF, Quina FH, Goncalves RS, Dupont J. Are molecular 5,8-pi-extended quinoxaline derivatives good chromophores for photoluminescence applications? European Journal of Organic Chemistry. 2006 ;( 21): 4924-4933.[citado 2024 out. 18 ]
    • Vancouver

      Mancilha FS, DaSilveira Neto BA, Lopes AS'A, Moreira Júnior PF, Quina FH, Goncalves RS, Dupont J. Are molecular 5,8-pi-extended quinoxaline derivatives good chromophores for photoluminescence applications? European Journal of Organic Chemistry. 2006 ;( 21): 4924-4933.[citado 2024 out. 18 ]
  • Source: Macromolecular Rapid Communications. Unidade: IQ

    Subjects: ESPECTROSCOPIA RAMAN, MATERIAIS NANOESTRUTURADOS

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    • ABNT

      DO NASCIMENTO, G. M. e SILVA, Claudio Hanashiro Barbosa e TEMPERINI, Márcia Laudelina Arruda. Electronic structure and doping behavior of PANI-NSA nanofibers investigated by resonance Raman spectroscopy. Macromolecular Rapid Communications, v. 27, n. 4, p. 255-259, 2006Tradução . . Acesso em: 18 out. 2024.
    • APA

      Do Nascimento, G. M., Silva, C. H. B., & Temperini, M. L. A. (2006). Electronic structure and doping behavior of PANI-NSA nanofibers investigated by resonance Raman spectroscopy. Macromolecular Rapid Communications, 27( 4), 255-259.
    • NLM

      Do Nascimento GM, Silva CHB, Temperini MLA. Electronic structure and doping behavior of PANI-NSA nanofibers investigated by resonance Raman spectroscopy. Macromolecular Rapid Communications. 2006 ; 27( 4): 255-259.[citado 2024 out. 18 ]
    • Vancouver

      Do Nascimento GM, Silva CHB, Temperini MLA. Electronic structure and doping behavior of PANI-NSA nanofibers investigated by resonance Raman spectroscopy. Macromolecular Rapid Communications. 2006 ; 27( 4): 255-259.[citado 2024 out. 18 ]
  • Source: European Journal of Inorganic Chemistry. Unidade: IQ

    Subjects: ELETROQUÍMICA, MANGANÊS, QUÍMICA SUPRAMOLECULAR

    How to cite
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    • ABNT

      MAYER, Ildemar et al. Steric and catalytic effects in tetraruthenated manganese porphyrins. European Journal of Inorganic Chemistry, n. 4, p. 850-856, 2006Tradução . . Acesso em: 18 out. 2024.
    • APA

      Mayer, I., Nunes, G. S., Toma, H. E., & Araki, K. (2006). Steric and catalytic effects in tetraruthenated manganese porphyrins. European Journal of Inorganic Chemistry, ( 4), 850-856.
    • NLM

      Mayer I, Nunes GS, Toma HE, Araki K. Steric and catalytic effects in tetraruthenated manganese porphyrins. European Journal of Inorganic Chemistry. 2006 ;( 4): 850-856.[citado 2024 out. 18 ]
    • Vancouver

      Mayer I, Nunes GS, Toma HE, Araki K. Steric and catalytic effects in tetraruthenated manganese porphyrins. European Journal of Inorganic Chemistry. 2006 ;( 4): 850-856.[citado 2024 out. 18 ]

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