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  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      SINGH, Fateh Veer e AMARAL, Mônica F. Z. J. e STEFANI, Hélio Alexandre. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides. Tetrahedron Letters, v. 50, n. 22, p. 2636-2639, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.03.078. Acesso em: 03 nov. 2024.
    • APA

      Singh, F. V., Amaral, M. F. Z. J., & Stefani, H. A. (2009). Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides. Tetrahedron Letters, 50( 22), 2636-2639. doi:10.1016/j.tetlet.2009.03.078
    • NLM

      Singh FV, Amaral MFZJ, Stefani HA. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides [Internet]. Tetrahedron Letters. 2009 ; 50( 22): 2636-2639.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
    • Vancouver

      Singh FV, Amaral MFZJ, Stefani HA. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides [Internet]. Tetrahedron Letters. 2009 ; 50( 22): 2636-2639.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
  • Source: Tetrahedron Letters. Unidades: FCF, IQ

    Subjects: SÍNTESE ORGÂNICA, TELÚRIO, PALÁDIO

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    • ABNT

      STEFANI, Hélio Alexandre et al. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, v. 50, n. 40, p. 5589-5595, 2009Tradução . . Acesso em: 03 nov. 2024.
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      Stefani, H. A., Pena, J. M., Gueogjian, K., Petragnani, N., Vaz, B. G., & Eberlin, M. N. (2009). Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, 50( 40), 5589-5595.
    • NLM

      Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 nov. 03 ]
    • Vancouver

      Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 nov. 03 ]
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, POTÁSSIO, PALÁDIO

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      WEBER, Minéia et al. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes. Tetrahedron Letters, v. 50, n. 30, p. 4324-4327, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.04.127. Acesso em: 03 nov. 2024.
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      Weber, M., Singh, F. V., Vieira, A. S., Stefani, H. A., & Paixão, M. W. (2009). Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes. Tetrahedron Letters, 50( 30), 4324-4327. doi:10.1016/j.tetlet.2009.04.127
    • NLM

      Weber M, Singh FV, Vieira AS, Stefani HA, Paixão MW. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4324-4327.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
    • Vancouver

      Weber M, Singh FV, Vieira AS, Stefani HA, Paixão MW. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4324-4327.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      SILVA, Márcio S. e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters, v. 50, n. 47, p. 6498-6501, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.09.023. Acesso em: 03 nov. 2024.
    • APA

      Silva, M. S., Santos, A. A. dos, & Comasseto, J. V. (2009). The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters, 50( 47), 6498-6501. doi:10.1016/j.tetlet.2009.09.023
    • NLM

      Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.09.023
    • Vancouver

      Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.09.023
  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      SINGH, Fateh Veer et al. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid. Tetrahedron Letters, v. 50, n. 20, p. 2312-2316, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.02.164. Acesso em: 03 nov. 2024.
    • APA

      Singh, F. V., Milagre, H. M. S., Eberlin, M. N., & Stefani, H. A. (2009). Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid. Tetrahedron Letters, 50( 20), 2312-2316. doi:10.1016/j.tetlet.2009.02.164
    • NLM

      Singh FV, Milagre HMS, Eberlin MN, Stefani HA. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid [Internet]. Tetrahedron Letters. 2009 ; 50( 20): 2312-2316.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
    • Vancouver

      Singh FV, Milagre HMS, Eberlin MN, Stefani HA. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid [Internet]. Tetrahedron Letters. 2009 ; 50( 20): 2312-2316.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: LÍTIO, CALCOGÊNIOS, SÍNTESE ORGÂNICA

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      KEPPLER, Artur Franz et al. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds. Tetrahedron Letters, v. 50, n. 19, p. 2181-2184, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.02.158. Acesso em: 03 nov. 2024.
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      Keppler, A. F., Gariani, R. A., Lopes, D. G., & Comasseto, J. V. (2009). Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds. Tetrahedron Letters, 50( 19), 2181-2184. doi:10.1016/j.tetlet.2009.02.158
    • NLM

      Keppler AF, Gariani RA, Lopes DG, Comasseto JV. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds [Internet]. Tetrahedron Letters. 2009 ; 50( 19): 2181-2184.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
    • Vancouver

      Keppler AF, Gariani RA, Lopes DG, Comasseto JV. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds [Internet]. Tetrahedron Letters. 2009 ; 50( 19): 2181-2184.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
  • Source: Tetrahedron. Unidade: FCF

    Subjects: ULTRASSONOGRAFIA, SÍNTESE ORGÂNICA

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      CELLA, Rodrigo e STEFANI, Hélio Alexandre. Ultrasound in heterocycles chemistry. Tetrahedron, v. 65, n. 13, p. 2619-2641, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.12.027. Acesso em: 03 nov. 2024.
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      Cella, R., & Stefani, H. A. (2009). Ultrasound in heterocycles chemistry. Tetrahedron, 65( 13), 2619-2641. doi:10.1016/j.tet.2008.12.027
    • NLM

      Cella R, Stefani HA. Ultrasound in heterocycles chemistry [Internet]. Tetrahedron. 2009 ; 65( 13): 2619-2641.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2008.12.027
    • Vancouver

      Cella R, Stefani HA. Ultrasound in heterocycles chemistry [Internet]. Tetrahedron. 2009 ; 65( 13): 2619-2641.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2008.12.027
  • 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: 03 nov. 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 nov. 03 ] 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 nov. 03 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf
  • Source: Tetrahedron. Unidade: FCF

    Subjects: POTÁSSIO (SÍNTESE), SÍNTESE ORGÂNICA

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      VIEIRA, Adriano Siqueira et al. Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions. Tetrahedron, v. 64, n. 30-31, p. 7234-7241, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.05.085. Acesso em: 03 nov. 2024.
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      Vieira, A. S., Fiorante, P. de F., Zukerman-Schpector, J., Alves, D., Botteselle, G. D. V., & Stefani, H. A. (2008). Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions. Tetrahedron, 64( 30-31), 7234-7241. doi:10.1016/j.tet.2008.05.085
    • NLM

      Vieira AS, Fiorante P de F, Zukerman-Schpector J, Alves D, Botteselle GDV, Stefani HA. Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions [Internet]. Tetrahedron. 2008 ; 64( 30-31): 7234-7241.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2008.05.085
    • Vancouver

      Vieira AS, Fiorante P de F, Zukerman-Schpector J, Alves D, Botteselle GDV, Stefani HA. Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions [Internet]. Tetrahedron. 2008 ; 64( 30-31): 7234-7241.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2008.05.085
  • Source: Tetrahedron. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, POTÁSSIO, SÍNTESE ORGÂNICA

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      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: 03 nov. 2024.
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      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. 03 ] 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. 03 ] Available from: https://doi.org/10.1016/j.tet.2008.02.006
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: ALDEÍDOS, SÍNTESE ORGÂNICA, BORO

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      CELLA, Rodrigo e VENTUROSO, Raphael Costa e STEFANI, Hélio Alexandre. Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes. Tetrahedron Letters, v. 49, n. 1, p. 16-19, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.11.031. Acesso em: 03 nov. 2024.
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      Cella, R., Venturoso, R. C., & Stefani, H. A. (2008). Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes. Tetrahedron Letters, 49( 1), 16-19. doi:10.1016/j.tetlet.2007.11.031
    • NLM

      Cella R, Venturoso RC, Stefani HA. Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes [Internet]. Tetrahedron Letters. 2008 ;49( 1): 16-19.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.031
    • Vancouver

      Cella R, Venturoso RC, Stefani HA. Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes [Internet]. Tetrahedron Letters. 2008 ;49( 1): 16-19.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.031
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, POTÁSSIO, COBRE, SÍNTESE ORGÂNICA

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      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: 03 nov. 2024.
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      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. 03 ] 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. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.083
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS

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      TOLEDO, Fabiano Travanca et al. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives. Tetrahedron Letters, v. 49, n. 5, p. 873-875, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.11.169. Acesso em: 03 nov. 2024.
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      Toledo, F. T., Cunha, R. L. O. R., Raminelli, C., & Comasseto, J. V. (2008). Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives. Tetrahedron Letters, 49( 5), 873-875. doi:10.1016/j.tetlet.2007.11.169
    • NLM

      Toledo FT, Cunha RLOR, Raminelli C, Comasseto JV. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives [Internet]. Tetrahedron Letters. 2008 ;49( 5): 873-875.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.169
    • Vancouver

      Toledo FT, Cunha RLOR, Raminelli C, Comasseto JV. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives [Internet]. Tetrahedron Letters. 2008 ;49( 5): 873-875.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.169
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: CATÁLISE, SÍNTESE ORGÂNICA

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      SCHWAB, Ricardo S. et al. Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide. Tetrahedron Letters, v. 49, n. 34, p. 5094-5097, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.06.031. Acesso em: 03 nov. 2024.
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      Schwab, R. S., Galetto, F. Z., Azeredo, J. B. de, Braga, A. L., Lüdtke, D. S., & Paixão, M. W. (2008). Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide. Tetrahedron Letters, 49( 34), 5094-5097. doi:10.1016/j.tetlet.2008.06.031
    • NLM

      Schwab RS, Galetto FZ, Azeredo JB de, Braga AL, Lüdtke DS, Paixão MW. Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide [Internet]. Tetrahedron Letters. 2008 ; 49( 34): 5094-5097.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2008.06.031
    • Vancouver

      Schwab RS, Galetto FZ, Azeredo JB de, Braga AL, Lüdtke DS, Paixão MW. Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide [Internet]. Tetrahedron Letters. 2008 ; 49( 34): 5094-5097.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2008.06.031
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: TELÚRIO, SÍNTESE ORGÂNICA

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      BASSORA, Bruno Karaski et al. Tellurium in organic synthesis: synthesis of bioactive butenolides. Tetrahedron Letters, v. 48, n. 8, p. 1485-1487, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.12.063. Acesso em: 03 nov. 2024.
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      Bassora, B. K., Da Costa, C. E., Gariani, R. A., Comasseto, J. V., & Dos Santos, A. A. (2007). Tellurium in organic synthesis: synthesis of bioactive butenolides. Tetrahedron Letters, 48( 8), 1485-1487. doi:10.1016/j.tetlet.2006.12.063
    • NLM

      Bassora BK, Da Costa CE, Gariani RA, Comasseto JV, Dos Santos AA. Tellurium in organic synthesis: synthesis of bioactive butenolides [Internet]. Tetrahedron Letters. 2007 ; 48( 8): 1485-1487.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2006.12.063
    • Vancouver

      Bassora BK, Da Costa CE, Gariani RA, Comasseto JV, Dos Santos AA. Tellurium in organic synthesis: synthesis of bioactive butenolides [Internet]. Tetrahedron Letters. 2007 ; 48( 8): 1485-1487.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2006.12.063
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: CANDIDA, SÍNTESE ORGÂNICA, ASPERGILLUS

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      OMORI, Álvaro Takeo et al. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435. Tetrahedron - Asymmetry, v. 18, n. 9, p. 1048-1053, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2007.04.019. Acesso em: 03 nov. 2024.
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      Omori, Á. T., Assis, L. F., Andrade, L. H., Comasseto, J. V., & Porto, A. L. M. (2007). Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435. Tetrahedron - Asymmetry, 18( 9), 1048-1053. doi:10.1016/j.tetasy.2007.04.019
    • NLM

      Omori ÁT, Assis LF, Andrade LH, Comasseto JV, Porto ALM. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1048-1053.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
    • Vancouver

      Omori ÁT, Assis LF, Andrade LH, Comasseto JV, Porto ALM. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1048-1053.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
  • Source: Synthesis. Unidade: IQ

    Subjects: TÁLIO, SÍNTESE ORGÂNICA

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    • ABNT

      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: 03 nov. 2024.
    • APA

      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 nov. 03 ]
    • 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 nov. 03 ]
  • Source: Tetrahedron. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, BORO

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    • ABNT

      STEFANI, Hélio Alexandre e CELLA, Rodrigo e VIEIRA, Adriano Siqueira. Recent advances in organotrifluoroborates chemistry. Tetrahedron, v. 63, n. 18, p. 3623-3658, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2007.01.061. Acesso em: 03 nov. 2024.
    • APA

      Stefani, H. A., Cella, R., & Vieira, A. S. (2007). Recent advances in organotrifluoroborates chemistry. Tetrahedron, 63( 18), 3623-3658. doi:10.1016/j.tet.2007.01.061
    • NLM

      Stefani HA, Cella R, Vieira AS. Recent advances in organotrifluoroborates chemistry [Internet]. Tetrahedron. 2007 ; 63( 18): 3623-3658.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2007.01.061
    • Vancouver

      Stefani HA, Cella R, Vieira AS. Recent advances in organotrifluoroborates chemistry [Internet]. Tetrahedron. 2007 ; 63( 18): 3623-3658.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2007.01.061
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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    • ABNT

      TOLEDO, Fabiano Travanca et al. The diorgano dichalcogenides addition to benzyne under mild conditions. Tetrahedron Letters, v. 48, n. 46, p. 8125-8127, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.09.111. Acesso em: 03 nov. 2024.
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      Toledo, F. T., Marques, H., Comasseto, J. V., & Raminelli, C. (2007). The diorgano dichalcogenides addition to benzyne under mild conditions. Tetrahedron Letters, 48( 46), 8125-8127. doi:10.1016/j.tetlet.2007.09.111
    • NLM

      Toledo FT, Marques H, Comasseto JV, Raminelli C. The diorgano dichalcogenides addition to benzyne under mild conditions [Internet]. Tetrahedron Letters. 2007 ; 48( 46): 8125-8127.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2007.09.111
    • Vancouver

      Toledo FT, Marques H, Comasseto JV, Raminelli C. The diorgano dichalcogenides addition to benzyne under mild conditions [Internet]. Tetrahedron Letters. 2007 ; 48( 46): 8125-8127.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2007.09.111
  • Source: Tetrahedron. Unidade: IQ

    Subjects: TELÚRIO, LÍTIO, SÍNTESE ORGÂNICA

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    • ABNT

      DOS SANTOS, Alcindo Aparecido et al. Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems. Tetrahedron, v. 63, n. 24, p. 5167-5172, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2007.03.178. Acesso em: 03 nov. 2024.
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      Dos Santos, A. A., Princival, J. L., Comasseto, J. V., Barros, S. M. G. de, & Brainer Neto, J. E. (2007). Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems. Tetrahedron, 63( 24), 5167-5172. doi:10.1016/j.tet.2007.03.178
    • NLM

      Dos Santos AA, Princival JL, Comasseto JV, Barros SMG de, Brainer Neto JE. Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems [Internet]. Tetrahedron. 2007 ; 63( 24): 5167-5172.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2007.03.178
    • Vancouver

      Dos Santos AA, Princival JL, Comasseto JV, Barros SMG de, Brainer Neto JE. Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems [Internet]. Tetrahedron. 2007 ; 63( 24): 5167-5172.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2007.03.178

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