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  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA

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      SASS, Daiane Cristina et al. Tandem reduction + cyclization of ortho-substituted cinnamic esters. Tetrahedron Letters, v. 52, n. 41, p. 5371-5374, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.08.039. Acesso em: 26 jun. 2024.
    • APA

      Sass, D. C., Lucca Júnior, E. C. de, Barbosa, J. da S., Oliveira, K. T. de, & Constantino, M. G. (2011). Tandem reduction + cyclization of ortho-substituted cinnamic esters. Tetrahedron Letters, 52( 41), 5371-5374. doi:10.1016/j.tetlet.2011.08.039
    • NLM

      Sass DC, Lucca Júnior EC de, Barbosa J da S, Oliveira KT de, Constantino MG. Tandem reduction + cyclization of ortho-substituted cinnamic esters [Internet]. Tetrahedron Letters. 2011 ; 52( 41): 5371-5374.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tetlet.2011.08.039
    • Vancouver

      Sass DC, Lucca Júnior EC de, Barbosa J da S, Oliveira KT de, Constantino MG. Tandem reduction + cyclization of ortho-substituted cinnamic esters [Internet]. Tetrahedron Letters. 2011 ; 52( 41): 5371-5374.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tetlet.2011.08.039
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA

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      NAZARIO, Carlos E. D. et al. Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator. Tetrahedron Letters, v. 52, n. 32, p. 4177-4181, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.06.004. Acesso em: 26 jun. 2024.
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      Nazario, C. E. D., Santana, A. S., Kawasoko, C. Y., Carollo, C. A., Hurtado, G. R., Viana, L. H., et al. (2011). Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator. Tetrahedron Letters, 52( 32), 4177-4181. doi:10.1016/j.tetlet.2011.06.004
    • NLM

      Nazario CED, Santana AS, Kawasoko CY, Carollo CA, Hurtado GR, Viana LH, Barbosa SL, Guerrero Junior PG, Marques FA, Dabdoub VB, Dabdoub MJ, Baroni ACM. Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator [Internet]. Tetrahedron Letters. 2011 ; 52( 32): 4177-4181.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tetlet.2011.06.004
    • Vancouver

      Nazario CED, Santana AS, Kawasoko CY, Carollo CA, Hurtado GR, Viana LH, Barbosa SL, Guerrero Junior PG, Marques FA, Dabdoub VB, Dabdoub MJ, Baroni ACM. Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator [Internet]. Tetrahedron Letters. 2011 ; 52( 32): 4177-4181.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tetlet.2011.06.004
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Subjects: FARMÁCIA, BIOQUÍMICA, QUÍMICA

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      DABDOUB, Miguel Joaquim et al. Synthesis of naturally occurring diene and trienes by Te/Li exchange on (1Z,3Z)-butyltelluro-4-methoxy-1,3-butadiene. Tetrahedron Letters, v. 51, n. 13, p. 1666-1670, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2010.01.066. Acesso em: 26 jun. 2024.
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      Dabdoub, M. J., Dabdoub, V. B., Baroni, A. C. de M., Hurtado, G. R., & Barbosa, S. L. (2010). Synthesis of naturally occurring diene and trienes by Te/Li exchange on (1Z,3Z)-butyltelluro-4-methoxy-1,3-butadiene. Tetrahedron Letters, 51( 13), 1666-1670. doi:10.1016/j.tetlet.2010.01.066
    • NLM

      Dabdoub MJ, Dabdoub VB, Baroni AC de M, Hurtado GR, Barbosa SL. Synthesis of naturally occurring diene and trienes by Te/Li exchange on (1Z,3Z)-butyltelluro-4-methoxy-1,3-butadiene [Internet]. Tetrahedron Letters. 2010 ; 51( 13): 1666-1670.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tetlet.2010.01.066
    • Vancouver

      Dabdoub MJ, Dabdoub VB, Baroni AC de M, Hurtado GR, Barbosa SL. Synthesis of naturally occurring diene and trienes by Te/Li exchange on (1Z,3Z)-butyltelluro-4-methoxy-1,3-butadiene [Internet]. Tetrahedron Letters. 2010 ; 51( 13): 1666-1670.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tetlet.2010.01.066
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Subjects: SÍNTESE ORGÂNICA, SILÊNCIO

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      DABDOUB, Miguel Joaquim et al. Total synthesis of ('+ OU -')-dihydroactinidiolide using selenium-stabilized carbenium ion. Tetrahedron Letters, v. 50, n. 40, p. 5569-5571, 2009Tradução . . Acesso em: 26 jun. 2024.
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      Dabdoub, M. J., Silveira, C. C., Lenardão, É. J., Guerrero Jr., P. G., Viana, L. H., Kawasoko, C. Y., & Baroni, A. C. M. (2009). Total synthesis of ('+ OU -')-dihydroactinidiolide using selenium-stabilized carbenium ion. Tetrahedron Letters, 50( 40), 5569-5571.
    • NLM

      Dabdoub MJ, Silveira CC, Lenardão ÉJ, Guerrero Jr. PG, Viana LH, Kawasoko CY, Baroni ACM. Total synthesis of ('+ OU -')-dihydroactinidiolide using selenium-stabilized carbenium ion. Tetrahedron Letters. 2009 ; 50( 40): 5569-5571.[citado 2024 jun. 26 ]
    • Vancouver

      Dabdoub MJ, Silveira CC, Lenardão ÉJ, Guerrero Jr. PG, Viana LH, Kawasoko CY, Baroni ACM. Total synthesis of ('+ OU -')-dihydroactinidiolide using selenium-stabilized carbenium ion. Tetrahedron Letters. 2009 ; 50( 40): 5569-5571.[citado 2024 jun. 26 ]
  • Source: Tetrahedron Letters. Unidades: FCFRP, FFCLRP

    Subjects: FÍSICO-QUÍMICA, PRODUTOS NATURAIS

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      SASS, Daiane Cristina et al. One-step biomimetic conversion of a furanoheliangolide into an eremantholide using Stryker's reagent. Tetrahedron Letters, v. 49, n. 24, p. 3877-3880, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.04.071. Acesso em: 26 jun. 2024.
    • APA

      Sass, D. C., Heleno, V. C. G., Lopes, J. L. C., & Constantino, M. G. (2008). One-step biomimetic conversion of a furanoheliangolide into an eremantholide using Stryker's reagent. Tetrahedron Letters, 49( 24), 3877-3880. doi:10.1016/j.tetlet.2008.04.071
    • NLM

      Sass DC, Heleno VCG, Lopes JLC, Constantino MG. One-step biomimetic conversion of a furanoheliangolide into an eremantholide using Stryker's reagent [Internet]. Tetrahedron Letters. 2008 ; 49( 24): 3877-3880.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tetlet.2008.04.071
    • Vancouver

      Sass DC, Heleno VCG, Lopes JLC, Constantino MG. One-step biomimetic conversion of a furanoheliangolide into an eremantholide using Stryker's reagent [Internet]. Tetrahedron Letters. 2008 ; 49( 24): 3877-3880.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tetlet.2008.04.071
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: REAÇÕES QUÍMICAS

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      GUERRERO JÚNIOR, Palimécio G. e DABDOUB, Miguel Joaquim e BARONI, Adriano C. M. Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals. Tetrahedron Letters, v. 49, n. 24, p. 3872-3876, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.04.072. Acesso em: 26 jun. 2024.
    • APA

      Guerrero Júnior, P. G., Dabdoub, M. J., & Baroni, A. C. M. (2008). Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals. Tetrahedron Letters, 49( 24), 3872-3876. doi:10.1016/j.tetlet.2008.04.072
    • NLM

      Guerrero Júnior PG, Dabdoub MJ, Baroni ACM. Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals [Internet]. Tetrahedron Letters. 2008 ; 49( 24): 3872-3876.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tetlet.2008.04.072
    • Vancouver

      Guerrero Júnior PG, Dabdoub MJ, Baroni ACM. Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals [Internet]. Tetrahedron Letters. 2008 ; 49( 24): 3872-3876.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tetlet.2008.04.072
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Subjects: PRODUTOS NATURAIS, SÍNTESE QUÍMICA

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    • ABNT

      SASS, Daiane Cristina e OLIVEIRA, Kleber Thiago de e CONSTANTINO, Maurício Gomes. Synthesis of homoallylic oxygenated "alfa"-methylene-"gama"-butyrolactones: a model for preparing biologically active natural lactones. Tetrahedron Letters, v. 49, n. 40, p. 5770-5772, 2008Tradução . . Acesso em: 26 jun. 2024.
    • APA

      Sass, D. C., Oliveira, K. T. de, & Constantino, M. G. (2008). Synthesis of homoallylic oxygenated "alfa"-methylene-"gama"-butyrolactones: a model for preparing biologically active natural lactones. Tetrahedron Letters, 49( 40), 5770-5772.
    • NLM

      Sass DC, Oliveira KT de, Constantino MG. Synthesis of homoallylic oxygenated "alfa"-methylene-"gama"-butyrolactones: a model for preparing biologically active natural lactones. Tetrahedron Letters. 2008 ; 49( 40): 5770-5772.[citado 2024 jun. 26 ]
    • Vancouver

      Sass DC, Oliveira KT de, Constantino MG. Synthesis of homoallylic oxygenated "alfa"-methylene-"gama"-butyrolactones: a model for preparing biologically active natural lactones. Tetrahedron Letters. 2008 ; 49( 40): 5770-5772.[citado 2024 jun. 26 ]
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA

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      RIBEIRO, Anderson O. et al. First phthalocyanine-'beta'-cyclodextrin dyads. Tetrahedron Letters, v. 47, p. 6129-6132, 2006Tradução . . Acesso em: 26 jun. 2024.
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      Ribeiro, A. O., Tomé, J. P. C., Neves, M. G. P. M. S., Tomé, A. C., Cavaleiro, J. A. S., Serra, O. A., & Torres, T. (2006). First phthalocyanine-'beta'-cyclodextrin dyads. Tetrahedron Letters, 47, 6129-6132.
    • NLM

      Ribeiro AO, Tomé JPC, Neves MGPMS, Tomé AC, Cavaleiro JAS, Serra OA, Torres T. First phthalocyanine-'beta'-cyclodextrin dyads. Tetrahedron Letters. 2006 ; 47 6129-6132.[citado 2024 jun. 26 ]
    • Vancouver

      Ribeiro AO, Tomé JPC, Neves MGPMS, Tomé AC, Cavaleiro JAS, Serra OA, Torres T. First phthalocyanine-'beta'-cyclodextrin dyads. Tetrahedron Letters. 2006 ; 47 6129-6132.[citado 2024 jun. 26 ]
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: SÍNTESE ORGÂNICA

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      SAIRRE, Mirela Inês e UHLE-BRONZE, Érika Soares e DONATE, Paulo Marcos. Niobium(V) oxide: a new and efficient catalyst for the transesterification of 'beta-keto' esters. Tetrahedron Letters, v. 46, p. 2705-2708, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2005.01.158. Acesso em: 26 jun. 2024.
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      Sairre, M. I., Uhle-Bronze, É. S., & Donate, P. M. (2005). Niobium(V) oxide: a new and efficient catalyst for the transesterification of 'beta-keto' esters. Tetrahedron Letters, 46, 2705-2708. doi:10.1016/j.tetlet.2005.01.158
    • NLM

      Sairre MI, Uhle-Bronze ÉS, Donate PM. Niobium(V) oxide: a new and efficient catalyst for the transesterification of 'beta-keto' esters [Internet]. Tetrahedron Letters. 2005 ; 46 2705-2708.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tetlet.2005.01.158
    • Vancouver

      Sairre MI, Uhle-Bronze ÉS, Donate PM. Niobium(V) oxide: a new and efficient catalyst for the transesterification of 'beta-keto' esters [Internet]. Tetrahedron Letters. 2005 ; 46 2705-2708.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tetlet.2005.01.158
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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      CONSTANTINO, Maurício Gomes et al. A synthetic approach to bicyclo[6.2.1] undecane ring systems. Tetrahedron Letters, v. 44, p. 2641-2643, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0040-4039(03)00377-0. Acesso em: 26 jun. 2024.
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      Constantino, M. G., Oliveira, K. T. de, Beatriz, A., & Silva, G. V. J. da. (2003). A synthetic approach to bicyclo[6.2.1] undecane ring systems. Tetrahedron Letters, 44, 2641-2643. doi:10.1016/s0040-4039(03)00377-0
    • NLM

      Constantino MG, Oliveira KT de, Beatriz A, Silva GVJ da. A synthetic approach to bicyclo[6.2.1] undecane ring systems [Internet]. Tetrahedron Letters. 2003 ; 44 2641-2643.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/s0040-4039(03)00377-0
    • Vancouver

      Constantino MG, Oliveira KT de, Beatriz A, Silva GVJ da. A synthetic approach to bicyclo[6.2.1] undecane ring systems [Internet]. Tetrahedron Letters. 2003 ; 44 2641-2643.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/s0040-4039(03)00377-0
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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      DABDOUB, Miguel Joaquim e DABDOUB, Vânia B. e LENARDÃO, Éder João. Synthesis of 1-methyl-4-alkyl-1,3-diacetylenes. Prototropic rearrangement in 1-alkyl-1,3-diacetylenes. Tetrahedron Letters, v. 42, p. 1807-1809, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0040-4039(01)00046-6. Acesso em: 26 jun. 2024.
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      Dabdoub, M. J., Dabdoub, V. B., & Lenardão, É. J. (2001). Synthesis of 1-methyl-4-alkyl-1,3-diacetylenes. Prototropic rearrangement in 1-alkyl-1,3-diacetylenes. Tetrahedron Letters, 42, 1807-1809. doi:10.1016/s0040-4039(01)00046-6
    • NLM

      Dabdoub MJ, Dabdoub VB, Lenardão ÉJ. Synthesis of 1-methyl-4-alkyl-1,3-diacetylenes. Prototropic rearrangement in 1-alkyl-1,3-diacetylenes [Internet]. Tetrahedron Letters. 2001 ; 42 1807-1809.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/s0040-4039(01)00046-6
    • Vancouver

      Dabdoub MJ, Dabdoub VB, Lenardão ÉJ. Synthesis of 1-methyl-4-alkyl-1,3-diacetylenes. Prototropic rearrangement in 1-alkyl-1,3-diacetylenes [Internet]. Tetrahedron Letters. 2001 ; 42 1807-1809.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/s0040-4039(01)00046-6
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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      DABDOUB, Miguel Joaquim e DABDOUB, Vânia B. e PEREIRA, Marco Antonio. Hydrochalcogenation of phenylthioacetylenes. Synthesis of mixed (Z)-trisubstituted 1,2-bis(organylchalcogeno)-1-alkenes. Tetrahedron Letters, v. 42, p. 1595-1597, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0040-4039(00)02291-7. Acesso em: 26 jun. 2024.
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      Dabdoub, M. J., Dabdoub, V. B., & Pereira, M. A. (2001). Hydrochalcogenation of phenylthioacetylenes. Synthesis of mixed (Z)-trisubstituted 1,2-bis(organylchalcogeno)-1-alkenes. Tetrahedron Letters, 42, 1595-1597. doi:10.1016/s0040-4039(00)02291-7
    • NLM

      Dabdoub MJ, Dabdoub VB, Pereira MA. Hydrochalcogenation of phenylthioacetylenes. Synthesis of mixed (Z)-trisubstituted 1,2-bis(organylchalcogeno)-1-alkenes [Internet]. Tetrahedron Letters. 2001 ; 42 1595-1597.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/s0040-4039(00)02291-7
    • Vancouver

      Dabdoub MJ, Dabdoub VB, Pereira MA. Hydrochalcogenation of phenylthioacetylenes. Synthesis of mixed (Z)-trisubstituted 1,2-bis(organylchalcogeno)-1-alkenes [Internet]. Tetrahedron Letters. 2001 ; 42 1595-1597.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/s0040-4039(00)02291-7
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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      DABDOUB, Miguel Joaquim e GUERRERO JÚNIOR, Palimécio Gimenes. Hydroalumination of phenylthioacetylenes. Synthesis and reaction of (Z)-and (E)-1-butyltelluro-1-phenylthio-1-alkenes. Tetrahedron Letters, v. 42, p. 7167-7172, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0040-4039(01)01511-8. Acesso em: 26 jun. 2024.
    • APA

      Dabdoub, M. J., & Guerrero Júnior, P. G. (2001). Hydroalumination of phenylthioacetylenes. Synthesis and reaction of (Z)-and (E)-1-butyltelluro-1-phenylthio-1-alkenes. Tetrahedron Letters, 42, 7167-7172. doi:10.1016/s0040-4039(01)01511-8
    • NLM

      Dabdoub MJ, Guerrero Júnior PG. Hydroalumination of phenylthioacetylenes. Synthesis and reaction of (Z)-and (E)-1-butyltelluro-1-phenylthio-1-alkenes [Internet]. Tetrahedron Letters. 2001 ; 42 7167-7172.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/s0040-4039(01)01511-8
    • Vancouver

      Dabdoub MJ, Guerrero Júnior PG. Hydroalumination of phenylthioacetylenes. Synthesis and reaction of (Z)-and (E)-1-butyltelluro-1-phenylthio-1-alkenes [Internet]. Tetrahedron Letters. 2001 ; 42 7167-7172.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/s0040-4039(01)01511-8
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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      CONSTANTINO, Maurício Gomes e BEATRIZ, Adilson e SILVA, Gil Valdo José da. A model synthesis of the bicyclic core structure of the furanoheliangolide sesquiterpenes. Tetrahedron Letters, v. 41, p. 7001-7004, 2000Tradução . . Disponível em: https://doi.org/10.1016/s0040-4039(00)01198-9. Acesso em: 26 jun. 2024.
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      Constantino, M. G., Beatriz, A., & Silva, G. V. J. da. (2000). A model synthesis of the bicyclic core structure of the furanoheliangolide sesquiterpenes. Tetrahedron Letters, 41, 7001-7004. doi:10.1016/s0040-4039(00)01198-9
    • NLM

      Constantino MG, Beatriz A, Silva GVJ da. A model synthesis of the bicyclic core structure of the furanoheliangolide sesquiterpenes [Internet]. Tetrahedron Letters. 2000 ; 41 7001-7004.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/s0040-4039(00)01198-9
    • Vancouver

      Constantino MG, Beatriz A, Silva GVJ da. A model synthesis of the bicyclic core structure of the furanoheliangolide sesquiterpenes [Internet]. Tetrahedron Letters. 2000 ; 41 7001-7004.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/s0040-4039(00)01198-9
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA

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      DABDOUB, Miguel Joaquim et al. Selectivity on the reaction of vinylic tellurides with butyllithium in the presence of carbonyl compounds. Tetrahedron Letters, v. 40, n. 40, p. 7159-7163, 1999Tradução . . Disponível em: https://doi.org/10.1016/s0040-4039(99)01567-1. Acesso em: 26 jun. 2024.
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      Dabdoub, M. J., Jacob, R. G., Ferreira, J. T. B., Dabdoub, V. B., & Marques, F. de A. (1999). Selectivity on the reaction of vinylic tellurides with butyllithium in the presence of carbonyl compounds. Tetrahedron Letters, 40( 40), 7159-7163. doi:10.1016/s0040-4039(99)01567-1
    • NLM

      Dabdoub MJ, Jacob RG, Ferreira JTB, Dabdoub VB, Marques F de A. Selectivity on the reaction of vinylic tellurides with butyllithium in the presence of carbonyl compounds [Internet]. Tetrahedron Letters. 1999 ; 40( 40): 7159-7163.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/s0040-4039(99)01567-1
    • Vancouver

      Dabdoub MJ, Jacob RG, Ferreira JTB, Dabdoub VB, Marques F de A. Selectivity on the reaction of vinylic tellurides with butyllithium in the presence of carbonyl compounds [Internet]. Tetrahedron Letters. 1999 ; 40( 40): 7159-7163.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/s0040-4039(99)01567-1

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