Filtros : "QUÍMICA FARMACÊUTICA" "Inglaterra" Removido: "IQSC" Limpar

Filtros



Refine with date range


  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, TELÚRIO, REAÇÕES ORGÂNICAS

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      GUADAGNIN, Rafael Carlos et al. Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts. Tetrahedron Letters, v. 49, n. 32, p. 4713-4716, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.05.129. Acesso em: 18 nov. 2024.
    • APA

      Guadagnin, R. C., Suganuma, C. A., Singh, F. V., Vieira, A. S., Cella, R., & Stefani, H. A. (2008). Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts. Tetrahedron Letters, 49( 32), 4713-4716. doi:10.1016/j.tetlet.2008.05.129
    • NLM

      Guadagnin RC, Suganuma CA, Singh FV, Vieira AS, Cella R, Stefani HA. Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts [Internet]. Tetrahedron Letters. 2008 ; 49( 32): 4713-4716.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.129
    • Vancouver

      Guadagnin RC, Suganuma CA, Singh FV, Vieira AS, Cella R, Stefani HA. Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts [Internet]. Tetrahedron Letters. 2008 ; 49( 32): 4713-4716.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.129
  • Source: Tetrahedron. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, POTÁSSIO, SÍNTESE ORGÂNICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      VIEIRA, Adriano Siqueira et al. Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles. Tetrahedron, v. 64, n. 15, p. 3306-3314, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.02.006. Acesso em: 18 nov. 2024.
    • APA

      Vieira, A. S., Ferreira, F. da P., Fiorante, P. de F., Guadagnin, R. C., & Stefani, H. A. (2008). Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles. Tetrahedron, 64( 15), 3306-3314. doi:10.1016/j.tet.2008.02.006
    • NLM

      Vieira AS, Ferreira F da P, Fiorante P de F, Guadagnin RC, Stefani HA. Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles [Internet]. Tetrahedron. 2008 ;64( 15): 3306-3314.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tet.2008.02.006
    • Vancouver

      Vieira AS, Ferreira F da P, Fiorante P de F, Guadagnin RC, Stefani HA. Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles [Internet]. Tetrahedron. 2008 ;64( 15): 3306-3314.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tet.2008.02.006
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, POTÁSSIO, COBRE, SÍNTESE ORGÂNICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      PAIXÃO, Márcio Weber et al. Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes. Tetrahedron Letters, v. 49, n. 15, p. 2366-2370, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.02.083. Acesso em: 18 nov. 2024.
    • APA

      Paixão, M. W., Weber, M., Braga, A. L., Azeredo, J. B. de, Deobald, A. M., & Stefani, H. A. (2008). Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes. Tetrahedron Letters, 49( 15), 2366-2370. doi:10.1016/j.tetlet.2008.02.083
    • NLM

      Paixão MW, Weber M, Braga AL, Azeredo JB de, Deobald AM, Stefani HA. Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2366-2370.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.083
    • Vancouver

      Paixão MW, Weber M, Braga AL, Azeredo JB de, Deobald AM, Stefani HA. Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2366-2370.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.083
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: ULTRASSONOGRAFIA, QUÍMICA FARMACÊUTICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      GUZEN, Karla Pierdoná e CELLA, Rodrigo e STEFANI, Hélio Alexandre. Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings. Tetrahedron Letters, v. 47, n. 46, p. 8133-8136, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.09.043. Acesso em: 18 nov. 2024.
    • APA

      Guzen, K. P., Cella, R., & Stefani, H. A. (2006). Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings. Tetrahedron Letters, 47( 46), 8133-8136. doi:10.1016/j.tetlet.2006.09.043
    • NLM

      Guzen KP, Cella R, Stefani HA. Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings [Internet]. Tetrahedron Letters. 2006 ; 47( 46): 8133-8136.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2006.09.043
    • Vancouver

      Guzen KP, Cella R, Stefani HA. Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings [Internet]. Tetrahedron Letters. 2006 ; 47( 46): 8133-8136.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2006.09.043
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: POTÁSSIO, TELÚRIO, QUÍMICA FARMACÊUTICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      STEFANI, Hélio Alexandre et al. Synthesis of 1,3-enynes via Suzuki-type reaction of vinylic tellurides and potassium alkynyltrifluoroborate salts. Tetrahedron Letters, v. 46, n. 4, p. 563-567, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2004.11.160. Acesso em: 18 nov. 2024.
    • APA

      Stefani, H. A., Cella, R., Dörr, F. A., Pereira, C. M. P. de, Zeni, G., & Gomes Junior, M. (2005). Synthesis of 1,3-enynes via Suzuki-type reaction of vinylic tellurides and potassium alkynyltrifluoroborate salts. Tetrahedron Letters, 46( 4), 563-567. doi:10.1016/j.tetlet.2004.11.160
    • NLM

      Stefani HA, Cella R, Dörr FA, Pereira CMP de, Zeni G, Gomes Junior M. Synthesis of 1,3-enynes via Suzuki-type reaction of vinylic tellurides and potassium alkynyltrifluoroborate salts [Internet]. Tetrahedron Letters. 2005 ; 46( 4): 563-567.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2004.11.160
    • Vancouver

      Stefani HA, Cella R, Dörr FA, Pereira CMP de, Zeni G, Gomes Junior M. Synthesis of 1,3-enynes via Suzuki-type reaction of vinylic tellurides and potassium alkynyltrifluoroborate salts [Internet]. Tetrahedron Letters. 2005 ; 46( 4): 563-567.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2004.11.160
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, HALOGENAÇÃO, COMPOSTOS HETEROCÍCLICOS

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      STEFANI, Hélio Alexandre et al. A mild and efficient method for halogenation of 3,5-dimethyl pyrazoles by ultrasound irradiation using N-halosuccinimides. Tetrahedron Letters, v. 46, n. 40, p. 6833-6837, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2005.08.027. Acesso em: 18 nov. 2024.
    • APA

      Stefani, H. A., Pereira, C. M. P. de, Almeida, R. B. de, Braga, R. de C., Guzen, K. P., & Cella, R. (2005). A mild and efficient method for halogenation of 3,5-dimethyl pyrazoles by ultrasound irradiation using N-halosuccinimides. Tetrahedron Letters, 46( 40), 6833-6837. doi:10.1016/j.tetlet.2005.08.027
    • NLM

      Stefani HA, Pereira CMP de, Almeida RB de, Braga R de C, Guzen KP, Cella R. A mild and efficient method for halogenation of 3,5-dimethyl pyrazoles by ultrasound irradiation using N-halosuccinimides [Internet]. Tetrahedron Letters. 2005 ; 46( 40): 6833-6837.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2005.08.027
    • Vancouver

      Stefani HA, Pereira CMP de, Almeida RB de, Braga R de C, Guzen KP, Cella R. A mild and efficient method for halogenation of 3,5-dimethyl pyrazoles by ultrasound irradiation using N-halosuccinimides [Internet]. Tetrahedron Letters. 2005 ; 46( 40): 6833-6837.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2005.08.027
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: ALDEÍDOS, ULTRASSONOGRAFIA, QUÍMICA FARMACÊUTICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      STEFANI, Hélio Alexandre et al. Ultrasound-assisted synthesis of functionalized arylacetylenes. Tetrahedron Letters, v. 46, n. 12, p. 2001-2003, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2005.01.161. Acesso em: 18 nov. 2024.
    • APA

      Stefani, H. A., Cella, R., Dörr, F. A., Pereira, C. M. P. de, Gomes, F. P., & Zeni, G. (2005). Ultrasound-assisted synthesis of functionalized arylacetylenes. Tetrahedron Letters, 46( 12), 2001-2003. doi:10.1016/j.tetlet.2005.01.161
    • NLM

      Stefani HA, Cella R, Dörr FA, Pereira CMP de, Gomes FP, Zeni G. Ultrasound-assisted synthesis of functionalized arylacetylenes [Internet]. Tetrahedron Letters. 2005 ; 46( 12): 2001-2003.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2005.01.161
    • Vancouver

      Stefani HA, Cella R, Dörr FA, Pereira CMP de, Gomes FP, Zeni G. Ultrasound-assisted synthesis of functionalized arylacetylenes [Internet]. Tetrahedron Letters. 2005 ; 46( 12): 2001-2003.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2005.01.161
  • Source: Organic & Biomolecular Chemistry. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, PALÁDIO, TELÚRIO

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      ZENI, Gilson et al. Stereoselective preparation of conjugated E-enynes from E-vinylic tellurides and terminal alkynes via Sonogashira cross-coupling. Organic & Biomolecular Chemistry, v. 2, n. 6, p. 803-805, 2004Tradução . . Acesso em: 18 nov. 2024.
    • APA

      Zeni, G., Alves, D., Pena, J. M., Braga, A. L., Stefani, H. A., & Nogueira, C. W. (2004). Stereoselective preparation of conjugated E-enynes from E-vinylic tellurides and terminal alkynes via Sonogashira cross-coupling. Organic & Biomolecular Chemistry, 2( 6), 803-805.
    • NLM

      Zeni G, Alves D, Pena JM, Braga AL, Stefani HA, Nogueira CW. Stereoselective preparation of conjugated E-enynes from E-vinylic tellurides and terminal alkynes via Sonogashira cross-coupling. Organic & Biomolecular Chemistry. 2004 ; 2( 6): 803-805.[citado 2024 nov. 18 ]
    • Vancouver

      Zeni G, Alves D, Pena JM, Braga AL, Stefani HA, Nogueira CW. Stereoselective preparation of conjugated E-enynes from E-vinylic tellurides and terminal alkynes via Sonogashira cross-coupling. Organic & Biomolecular Chemistry. 2004 ; 2( 6): 803-805.[citado 2024 nov. 18 ]
  • Source: Bioorganic and Medicinal Chemistry Letters. Unidade: IQ

    Subjects: QUÍMICA FARMACÊUTICA, SEROTONINA, BIOQUÍMICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      RAHMAN, Ashraf A. et al. Conformationally-restricted analogues and partition coefficients of the '5-HT IND. 3' serotonin receptor ligands Meta-chlorophenylbiguanide (mCPBG) and Meta-chlorophenylguanidine (mCPG). Bioorganic and Medicinal Chemistry Letters, v. 13, n. 6, p. 1119-1123, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0960-894x(03)00044-1. Acesso em: 18 nov. 2024.
    • APA

      Rahman, A. A., Daoud, M. K., Dukat, M., Herrick-Davis, K., Purohit, A., Teitler, M., et al. (2003). Conformationally-restricted analogues and partition coefficients of the '5-HT IND. 3' serotonin receptor ligands Meta-chlorophenylbiguanide (mCPBG) and Meta-chlorophenylguanidine (mCPG). Bioorganic and Medicinal Chemistry Letters, 13( 6), 1119-1123. doi:10.1016/s0960-894x(03)00044-1
    • NLM

      Rahman AA, Daoud MK, Dukat M, Herrick-Davis K, Purohit A, Teitler M, Amaral AT do, Malvezzi A, Glennon RA. Conformationally-restricted analogues and partition coefficients of the '5-HT IND. 3' serotonin receptor ligands Meta-chlorophenylbiguanide (mCPBG) and Meta-chlorophenylguanidine (mCPG) [Internet]. Bioorganic and Medicinal Chemistry Letters. 2003 ; 13( 6): 1119-1123.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/s0960-894x(03)00044-1
    • Vancouver

      Rahman AA, Daoud MK, Dukat M, Herrick-Davis K, Purohit A, Teitler M, Amaral AT do, Malvezzi A, Glennon RA. Conformationally-restricted analogues and partition coefficients of the '5-HT IND. 3' serotonin receptor ligands Meta-chlorophenylbiguanide (mCPBG) and Meta-chlorophenylguanidine (mCPG) [Internet]. Bioorganic and Medicinal Chemistry Letters. 2003 ; 13( 6): 1119-1123.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/s0960-894x(03)00044-1
  • Source: Bioorganic and Medicinal Chemistry. Unidades: IQ, FCF

    Subjects: QUÍMICA FARMACÊUTICA, FARMÁCIA, ANTIBIÓTICOS, INFECÇÕES BACTERIANAS

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      RANDO, Daniela Gonçales et al. Potential tuberculostatic agents. Topliss application on benzoic acid [(5-nitro-thiophen-2-yl)-methylene]-hydrazide series. Bioorganic and Medicinal Chemistry, v. 10, n. 3, p. 557-560, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0968-0896(01)00313-3. Acesso em: 18 nov. 2024.
    • APA

      Rando, D. G., Sato, D. N., Siqueira, L., Malvezzi, A., Leite, C. Q. F., Amaral, A. T. do, et al. (2002). Potential tuberculostatic agents. Topliss application on benzoic acid [(5-nitro-thiophen-2-yl)-methylene]-hydrazide series. Bioorganic and Medicinal Chemistry, 10( 3), 557-560. doi:10.1016/s0968-0896(01)00313-3
    • NLM

      Rando DG, Sato DN, Siqueira L, Malvezzi A, Leite CQF, Amaral AT do, Ferreira EI, Tavares LC. Potential tuberculostatic agents. Topliss application on benzoic acid [(5-nitro-thiophen-2-yl)-methylene]-hydrazide series [Internet]. Bioorganic and Medicinal Chemistry. 2002 ; 10( 3): 557-560.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/s0968-0896(01)00313-3
    • Vancouver

      Rando DG, Sato DN, Siqueira L, Malvezzi A, Leite CQF, Amaral AT do, Ferreira EI, Tavares LC. Potential tuberculostatic agents. Topliss application on benzoic acid [(5-nitro-thiophen-2-yl)-methylene]-hydrazide series [Internet]. Bioorganic and Medicinal Chemistry. 2002 ; 10( 3): 557-560.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/s0968-0896(01)00313-3

Digital Library of Intellectual Production of Universidade de São Paulo     2012 - 2024