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  • Source: Tetrahedron. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, SESQUITERPENOS

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    • ABNT

      FERRAZ, Helena Maria Carvalho e AGUILAR, Andrea Maria e SILVA JR., Luiz Fernando da. A diastereoselective total synthesis of the sesquiterpene (+or-)-mutisianthol. Tetrahedron, v. 59, n. 31, p. 5817-5821, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(03)00974-8. Acesso em: 06 jul. 2024.
    • APA

      Ferraz, H. M. C., Aguilar, A. M., & Silva Jr., L. F. da. (2003). A diastereoselective total synthesis of the sesquiterpene (+or-)-mutisianthol. Tetrahedron, 59( 31), 5817-5821. doi:10.1016/s0040-4020(03)00974-8
    • NLM

      Ferraz HMC, Aguilar AM, Silva Jr. LF da. A diastereoselective total synthesis of the sesquiterpene (+or-)-mutisianthol [Internet]. Tetrahedron. 2003 ; 59( 31): 5817-5821.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(03)00974-8
    • Vancouver

      Ferraz HMC, Aguilar AM, Silva Jr. LF da. A diastereoselective total synthesis of the sesquiterpene (+or-)-mutisianthol [Internet]. Tetrahedron. 2003 ; 59( 31): 5817-5821.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(03)00974-8
  • Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, REAÇÕES ORGÂNICAS

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    • ABNT

      SILVA JR., Luiz Fernando da. Construction of cyclopentyl units by ring contraction reactions. Tetrahedron, v. 58, n. 45, p. 9137-9161, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(02)00990-0. Acesso em: 06 jul. 2024.
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      Silva Jr., L. F. da. (2002). Construction of cyclopentyl units by ring contraction reactions. Tetrahedron, 58( 45), 9137-9161. doi:10.1016/s0040-4020(02)00990-0
    • NLM

      Silva Jr. LF da. Construction of cyclopentyl units by ring contraction reactions [Internet]. Tetrahedron. 2002 ; 58( 45): 9137-9161.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(02)00990-0
    • Vancouver

      Silva Jr. LF da. Construction of cyclopentyl units by ring contraction reactions [Internet]. Tetrahedron. 2002 ; 58( 45): 9137-9161.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(02)00990-0
  • Source: Tetrahedron. Unidade: IQSC

    Assunto: QUÍMICA TEÓRICA

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    • ABNT

      ALVES, C. N. et al. An AM1 theoretical study on the effect of 'Zn POT.2+' Lewis acid catalysis on the mechanism of the cycloaddition between 3-phenyl-1-(2-pyridyl)-2-propen-1-one and cyclopentadiene. Tetrahedron, v. 58, n. 13, p. 2695-2700, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(02)00072-8. Acesso em: 06 jul. 2024.
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      Alves, C. N., Silva, A. B. F. da, Martí, S., Moliner, V., Oliva, M., Andrés, J., & Domingo, L. R. (2002). An AM1 theoretical study on the effect of 'Zn POT.2+' Lewis acid catalysis on the mechanism of the cycloaddition between 3-phenyl-1-(2-pyridyl)-2-propen-1-one and cyclopentadiene. Tetrahedron, 58( 13), 2695-2700. doi:10.1016/s0040-4020(02)00072-8
    • NLM

      Alves CN, Silva ABF da, Martí S, Moliner V, Oliva M, Andrés J, Domingo LR. An AM1 theoretical study on the effect of 'Zn POT.2+' Lewis acid catalysis on the mechanism of the cycloaddition between 3-phenyl-1-(2-pyridyl)-2-propen-1-one and cyclopentadiene [Internet]. Tetrahedron. 2002 ; 58( 13): 2695-2700.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(02)00072-8
    • Vancouver

      Alves CN, Silva ABF da, Martí S, Moliner V, Oliva M, Andrés J, Domingo LR. An AM1 theoretical study on the effect of 'Zn POT.2+' Lewis acid catalysis on the mechanism of the cycloaddition between 3-phenyl-1-(2-pyridyl)-2-propen-1-one and cyclopentadiene [Internet]. Tetrahedron. 2002 ; 58( 13): 2695-2700.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(02)00072-8
  • Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, QUÍMICA INORGÂNICA, TELÚRIO, COMPOSTOS ORGANOMETÁLICOS, REAÇÕES ORGÂNICAS, ESTEREOQUÍMICA

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    • ABNT

      BARRIENTOS-ASTIGARRAGA, Rafael Eliseo et al. A general method of synthesis of functionalized Z-vinylic tellurides starting from beta-dicarbonyl compounds. Tetrahedron, v. 58, n. 6, p. 1051-1059, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(01)01204-2. Acesso em: 06 jul. 2024.
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      Barrientos-Astigarraga, R. E., Castelani, P., Sumida, C. Y., Zukerman-Schpector, J., & Comasseto, J. V. (2002). A general method of synthesis of functionalized Z-vinylic tellurides starting from beta-dicarbonyl compounds. Tetrahedron, 58( 6), 1051-1059. doi:10.1016/s0040-4020(01)01204-2
    • NLM

      Barrientos-Astigarraga RE, Castelani P, Sumida CY, Zukerman-Schpector J, Comasseto JV. A general method of synthesis of functionalized Z-vinylic tellurides starting from beta-dicarbonyl compounds [Internet]. Tetrahedron. 2002 ; 58( 6): 1051-1059.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(01)01204-2
    • Vancouver

      Barrientos-Astigarraga RE, Castelani P, Sumida CY, Zukerman-Schpector J, Comasseto JV. A general method of synthesis of functionalized Z-vinylic tellurides starting from beta-dicarbonyl compounds [Internet]. Tetrahedron. 2002 ; 58( 6): 1051-1059.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(01)01204-2
  • Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, OXIDAÇÃO, TÁLIO

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    • ABNT

      FERRAZ, Helena Maria Carvalho e SILVA JUNIOR, Luiz Fernando da e VIEIRA, Tiago O. Thallium trinitrate-mediated ring contaction of 1,2-dihydronaphthalenes: an approach to the synthesis of indans. Tetrahedron, v. 57, n. 9, p. 1709-1713, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(00)01174-1. Acesso em: 06 jul. 2024.
    • APA

      Ferraz, H. M. C., Silva Junior, L. F. da, & Vieira, T. O. (2001). Thallium trinitrate-mediated ring contaction of 1,2-dihydronaphthalenes: an approach to the synthesis of indans. Tetrahedron, 57( 9), 1709-1713. doi:10.1016/s0040-4020(00)01174-1
    • NLM

      Ferraz HMC, Silva Junior LF da, Vieira TO. Thallium trinitrate-mediated ring contaction of 1,2-dihydronaphthalenes: an approach to the synthesis of indans [Internet]. Tetrahedron. 2001 ; 57( 9): 1709-1713.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(00)01174-1
    • Vancouver

      Ferraz HMC, Silva Junior LF da, Vieira TO. Thallium trinitrate-mediated ring contaction of 1,2-dihydronaphthalenes: an approach to the synthesis of indans [Internet]. Tetrahedron. 2001 ; 57( 9): 1709-1713.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(00)01174-1
  • Source: 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: 06 jul. 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 jul. 06 ] 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 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(01)00337-4
  • Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, REAÇÕES ORGÂNICAS, SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS, COMPOSTOS ORGANOMETÁLICOS, TÁLIO

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    • ABNT

      FERRAZ, Helena Maria Carvalho e SILVA JR., Luiz Fernando da. Construction of functionalized indans by thallium(III) promoted ring contraction of 3-alkenols. Tetrahedron, v. 57, n. 50, p. 9939-9949, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(01)01021-3. Acesso em: 06 jul. 2024.
    • APA

      Ferraz, H. M. C., & Silva Jr., L. F. da. (2001). Construction of functionalized indans by thallium(III) promoted ring contraction of 3-alkenols. Tetrahedron, 57( 50), 9939-9949. doi:10.1016/s0040-4020(01)01021-3
    • NLM

      Ferraz HMC, Silva Jr. LF da. Construction of functionalized indans by thallium(III) promoted ring contraction of 3-alkenols [Internet]. Tetrahedron. 2001 ; 57( 50): 9939-9949.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(01)01021-3
    • Vancouver

      Ferraz HMC, Silva Jr. LF da. Construction of functionalized indans by thallium(III) promoted ring contraction of 3-alkenols [Internet]. Tetrahedron. 2001 ; 57( 50): 9939-9949.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(01)01021-3
  • Source: Tetrahedron. Unidades: IQ, FCF

    Assunto: FARMACOLOGIA

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      PETRAGNANI, Nicola e STEFANI, Hélio Alexandre e VALDUGA, Claudete Justina. Recent advances in selenocyclofunctionalization reactions. Tetrahedron, v. 57, n. 8, p. 1411-1448, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(00)01033-4. Acesso em: 06 jul. 2024.
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      Petragnani, N., Stefani, H. A., & Valduga, C. J. (2001). Recent advances in selenocyclofunctionalization reactions. Tetrahedron, 57( 8), 1411-1448. doi:10.1016/s0040-4020(00)01033-4
    • NLM

      Petragnani N, Stefani HA, Valduga CJ. Recent advances in selenocyclofunctionalization reactions [Internet]. Tetrahedron. 2001 ; 57( 8): 1411-1448.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(00)01033-4
    • Vancouver

      Petragnani N, Stefani HA, Valduga CJ. Recent advances in selenocyclofunctionalization reactions [Internet]. Tetrahedron. 2001 ; 57( 8): 1411-1448.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(00)01033-4
  • Source: Tetrahedron. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      NERY, Ana Luíza Petillo et al. Studies on the intramolecular electron transfer catalyzed thermolysis of 1, 2- dioxetanes. Tetrahedron, v. 56, n. 30, p. 5317-5327, 2000Tradução . . Disponível em: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v56i0030&article=5317_sotietcto1&form=pdf&file=file.pdf. Acesso em: 06 jul. 2024.
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      Nery, A. L. P., Weib, D., Catalani, L. H., & Baader, W. J. (2000). Studies on the intramolecular electron transfer catalyzed thermolysis of 1, 2- dioxetanes. Tetrahedron, 56( 30), 5317-5327. Recuperado de http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v56i0030&article=5317_sotietcto1&form=pdf&file=file.pdf
    • NLM

      Nery ALP, Weib D, Catalani LH, Baader WJ. Studies on the intramolecular electron transfer catalyzed thermolysis of 1, 2- dioxetanes [Internet]. Tetrahedron. 2000 ; 56( 30): 5317-5327.[citado 2024 jul. 06 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v56i0030&article=5317_sotietcto1&form=pdf&file=file.pdf
    • Vancouver

      Nery ALP, Weib D, Catalani LH, Baader WJ. Studies on the intramolecular electron transfer catalyzed thermolysis of 1, 2- dioxetanes [Internet]. Tetrahedron. 2000 ; 56( 30): 5317-5327.[citado 2024 jul. 06 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v56i0030&article=5317_sotietcto1&form=pdf&file=file.pdf
  • Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, FOSFATOS

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    • ABNT

      MORAES, D. N. et al. Addition of Z-Vinylic higher order cyanocuprates to enones followed by O-functionalization. Tetrahedron, v. 56, n. 21, p. 3327-3337, 2000Tradução . . Acesso em: 06 jul. 2024.
    • APA

      Moraes, D. N., Barrientos-Astigarraga, R. E., Castelani, P., & Comasseto, J. V. (2000). Addition of Z-Vinylic higher order cyanocuprates to enones followed by O-functionalization. Tetrahedron, 56( 21), 3327-3337.
    • NLM

      Moraes DN, Barrientos-Astigarraga RE, Castelani P, Comasseto JV. Addition of Z-Vinylic higher order cyanocuprates to enones followed by O-functionalization. Tetrahedron. 2000 ; 56( 21): 3327-3337.[citado 2024 jul. 06 ]
    • Vancouver

      Moraes DN, Barrientos-Astigarraga RE, Castelani P, Comasseto JV. Addition of Z-Vinylic higher order cyanocuprates to enones followed by O-functionalization. Tetrahedron. 2000 ; 56( 21): 3327-3337.[citado 2024 jul. 06 ]
  • Source: Tetrahedron. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      FERRAZ, Helena Maria Carvalho et al. Synthesis of N-substituted pyrrole and tetrahydroindole derivatives from alkenyl `beta´-dicarbonyl compounds. Tetrahedron, v. 55, n. 36, p. 10915-10924, 1999Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(99)00625-0. Acesso em: 06 jul. 2024.
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      Ferraz, H. M. C., Pereira, F. L. C., Leite, F. S., Nunes, M. R. S., & Payret-Arrúa, M. E. (1999). Synthesis of N-substituted pyrrole and tetrahydroindole derivatives from alkenyl `beta´-dicarbonyl compounds. Tetrahedron, 55( 36), 10915-10924. doi:10.1016/s0040-4020(99)00625-0
    • NLM

      Ferraz HMC, Pereira FLC, Leite FS, Nunes MRS, Payret-Arrúa ME. Synthesis of N-substituted pyrrole and tetrahydroindole derivatives from alkenyl `beta´-dicarbonyl compounds [Internet]. Tetrahedron. 1999 ; 55( 36): 10915-10924.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(99)00625-0
    • Vancouver

      Ferraz HMC, Pereira FLC, Leite FS, Nunes MRS, Payret-Arrúa ME. Synthesis of N-substituted pyrrole and tetrahydroindole derivatives from alkenyl `beta´-dicarbonyl compounds [Internet]. Tetrahedron. 1999 ; 55( 36): 10915-10924.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(99)00625-0
  • Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, QUÍMICA INORGÂNICA

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      WLADISLAW, Blanka et al. Sulfenylation of `beta´-keto sulfoxides. III. Diastereoselectivity induced by a chiral phase transfer catalyst. Tetrahedron, v. 55, n. 41, p. 12023-12030, 1999Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(99)00705-x. Acesso em: 06 jul. 2024.
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      Wladislaw, B., Marzorati, L., Biaggio, F. C., Vargas, R. R., Bjorklund, M. B., & Zukerman-Schpector, J. (1999). Sulfenylation of `beta´-keto sulfoxides. III. Diastereoselectivity induced by a chiral phase transfer catalyst. Tetrahedron, 55( 41), 12023-12030. doi:10.1016/s0040-4020(99)00705-x
    • NLM

      Wladislaw B, Marzorati L, Biaggio FC, Vargas RR, Bjorklund MB, Zukerman-Schpector J. Sulfenylation of `beta´-keto sulfoxides. III. Diastereoselectivity induced by a chiral phase transfer catalyst [Internet]. Tetrahedron. 1999 ; 55( 41): 12023-12030.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(99)00705-x
    • Vancouver

      Wladislaw B, Marzorati L, Biaggio FC, Vargas RR, Bjorklund MB, Zukerman-Schpector J. Sulfenylation of `beta´-keto sulfoxides. III. Diastereoselectivity induced by a chiral phase transfer catalyst [Internet]. Tetrahedron. 1999 ; 55( 41): 12023-12030.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/s0040-4020(99)00705-x

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