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  • Artigo de periodico

    Micellar effects and analytical applications of nitro substitution in 4-Nitro-N-alkyl-1,8-naphthalimide by cysteine derivatives (2020)

    Martins, V. S; Triboni, Eduardo Rezende ; Bonilha, João Baptista Sargi; Gonçalves, L.M; Mortara, L; Carvalho, L. A. C; Manda, B. R; Lacerda, C. D; Meotti, Flavia Carla ; Politi, Mário José ; Chaimovich Guralnik, Hernan ; Cuccovia, Iolanda Midea

    Source: Heliyon. Unidades: EEL, IQ

    Subjects: FLUORESCÊNCIA, QUÍMICA ORGÂNICA, QUÍMICA ANALÍTICA

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      MARTINS, V. S et al. Micellar effects and analytical applications of nitro substitution in 4-Nitro-N-alkyl-1,8-naphthalimide by cysteine derivatives. Heliyon, v. 6, p. 1-14 art. e04938, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.heliyon.2020.e04938. Acesso em: 31 jul. 2024.

    • APA

      Martins, V. S., Triboni, E. R., Bonilha, J. B. S., Gonçalves, L. M., Mortara, L., Carvalho, L. A. C., et al. (2020). Micellar effects and analytical applications of nitro substitution in 4-Nitro-N-alkyl-1,8-naphthalimide by cysteine derivatives. Heliyon, 6, 1-14 art. e04938. doi:10.1016/j.heliyon.2020.e04938

    • NLM

      Martins VS, Triboni ER, Bonilha JBS, Gonçalves LM, Mortara L, Carvalho LAC, Manda BR, Lacerda CD, Meotti FC, Politi MJ, Chaimovich Guralnik H, Cuccovia IM. Micellar effects and analytical applications of nitro substitution in 4-Nitro-N-alkyl-1,8-naphthalimide by cysteine derivatives [Internet]. Heliyon. 2020 ; 6 1-14 art. e04938.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.heliyon.2020.e04938

    • Vancouver

      Martins VS, Triboni ER, Bonilha JBS, Gonçalves LM, Mortara L, Carvalho LAC, Manda BR, Lacerda CD, Meotti FC, Politi MJ, Chaimovich Guralnik H, Cuccovia IM. Micellar effects and analytical applications of nitro substitution in 4-Nitro-N-alkyl-1,8-naphthalimide by cysteine derivatives [Internet]. Heliyon. 2020 ; 6 1-14 art. e04938.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.heliyon.2020.e04938

  • Artigo de periodico

    An efficient approach for the synthesis of new (±)-coixspirolactams (2020)

    Nascimento, Vinicius Rodrigues do; Suenaga, Melissa L. S; Andrade, Leandro Helgueira

    Source: Organic & Biomolecular Chemistry. Unidade: IQ

    Subjects: ALCALOIDES, QUÍMICA ORGÂNICA

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    • ABNT

      NASCIMENTO, Vinicius Rodrigues do e SUENAGA, Melissa L. S e ANDRADE, Leandro Helgueira. An efficient approach for the synthesis of new (±)-coixspirolactams. Organic & Biomolecular Chemistry, v. 18, p. 5458-5465, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0ob01104e. Acesso em: 31 jul. 2024.

    • APA

      Nascimento, V. R. do, Suenaga, M. L. S., & Andrade, L. H. (2020). An efficient approach for the synthesis of new (±)-coixspirolactams. Organic & Biomolecular Chemistry, 18, 5458-5465. doi:10.1039/d0ob01104e

    • NLM

      Nascimento VR do, Suenaga MLS, Andrade LH. An efficient approach for the synthesis of new (±)-coixspirolactams [Internet]. Organic & Biomolecular Chemistry. 2020 ; 18 5458-5465.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1039/d0ob01104e

    • Vancouver

      Nascimento VR do, Suenaga MLS, Andrade LH. An efficient approach for the synthesis of new (±)-coixspirolactams [Internet]. Organic & Biomolecular Chemistry. 2020 ; 18 5458-5465.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1039/d0ob01104e

  • Artigo de periodico

    2-[(4-Chlorophenyl)sulfanyl]-2-methoxy-1-phenyl-ethan-1-one: crystal structure and Hirshfeld surface analysis (2018)

    Caracelli, Ignez; Schpector, Júlio Zukerman; Traesel, Henrique Joel; Olivato, Paulo Roberto ; Jotani , Mukesh M; Tiekink, Edward R. T

    Source: Acta Crystallographica Section E. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, QUÍMICA DE SUPERFÍCIE

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    • ABNT

      CARACELLI, Ignez et al. 2-[(4-Chlorophenyl)sulfanyl]-2-methoxy-1-phenyl-ethan-1-one: crystal structure and Hirshfeld surface analysis. Acta Crystallographica Section E, v. 74 , n. 5, p. 703-708 :+ Supplementary materials (S1-S4), 2018Tradução . . Disponível em: https://doi.org/10.1107/S2056989018006072. Acesso em: 31 jul. 2024.

    • APA

      Caracelli, I., Schpector, J. Z., Traesel, H. J., Olivato, P. R., Jotani , M. M., & Tiekink, E. R. T. (2018). 2-[(4-Chlorophenyl)sulfanyl]-2-methoxy-1-phenyl-ethan-1-one: crystal structure and Hirshfeld surface analysis. Acta Crystallographica Section E, 74 ( 5), 703-708 :+ Supplementary materials (S1-S4). doi:10.1107/S2056989018006072

    • NLM

      Caracelli I, Schpector JZ, Traesel HJ, Olivato PR, Jotani MM, Tiekink ERT. 2-[(4-Chlorophenyl)sulfanyl]-2-methoxy-1-phenyl-ethan-1-one: crystal structure and Hirshfeld surface analysis [Internet]. Acta Crystallographica Section E. 2018 ; 74 ( 5): 703-708 :+ Supplementary materials (S1-S4).[citado 2024 jul. 31 ] Available from: https://doi.org/10.1107/S2056989018006072

    • Vancouver

      Caracelli I, Schpector JZ, Traesel HJ, Olivato PR, Jotani MM, Tiekink ERT. 2-[(4-Chlorophenyl)sulfanyl]-2-methoxy-1-phenyl-ethan-1-one: crystal structure and Hirshfeld surface analysis [Internet]. Acta Crystallographica Section E. 2018 ; 74 ( 5): 703-708 :+ Supplementary materials (S1-S4).[citado 2024 jul. 31 ] Available from: https://doi.org/10.1107/S2056989018006072

  • Trabalho de evento-resumo

    Electrophilic alkynylation using hypervalent iodine reagents (2017)

    Teodoro, Bruno Vinicius Motta; Silva Junior, Luiz Fernando da

    Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ

    Subjects: REAGENTES ORGÂNICOS, QUÍMICA ORGÂNICA

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    • ABNT

      TEODORO, Bruno Vinicius Motta e SILVA JUNIOR, Luiz Fernando da. Electrophilic alkynylation using hypervalent iodine reagents. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 31 jul. 2024.

    • APA

      Teodoro, B. V. M., & Silva Junior, L. F. da. (2017). Electrophilic alkynylation using hypervalent iodine reagents. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/

    • NLM

      Teodoro BVM, Silva Junior LF da. Electrophilic alkynylation using hypervalent iodine reagents [Internet]. Proceedings. 2017 ;[citado 2024 jul. 31 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/

    • Vancouver

      Teodoro BVM, Silva Junior LF da. Electrophilic alkynylation using hypervalent iodine reagents [Internet]. Proceedings. 2017 ;[citado 2024 jul. 31 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/

  • Trabalho de evento-resumo

    Cyclofunctionalizations using iodine/iodine(III) (2017)

    Scarassati Filho, Paulo; Silva Junior, Luiz Fernando da

    Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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    • ABNT

      SCARASSATI FILHO, Paulo e SILVA JUNIOR, Luiz Fernando da. Cyclofunctionalizations using iodine/iodine(III). 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 31 jul. 2024.

    • APA

      Scarassati Filho, P., & Silva Junior, L. F. da. (2017). Cyclofunctionalizations using iodine/iodine(III). In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/

    • NLM

      Scarassati Filho P, Silva Junior LF da. Cyclofunctionalizations using iodine/iodine(III) [Internet]. Proceedings. 2017 ;[citado 2024 jul. 31 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/

    • Vancouver

      Scarassati Filho P, Silva Junior LF da. Cyclofunctionalizations using iodine/iodine(III) [Internet]. Proceedings. 2017 ;[citado 2024 jul. 31 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/

  • Artigo de periodico

    On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds (2016)

    Avila, Thais C; Reginato, Marcelo M; Di Vitta, Cláudio ; Ducati, Lucas Colucci ; Andrade, Leandro Helgueira ; Marzorati, Liliana

    Source: Tetrahedrom Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, COMPOSTOS ORGÂNICOS

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      AVILA, Thais C et al. On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds. Tetrahedrom Letters, v. 57, p. 2152-2157, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.03.109. Acesso em: 31 jul. 2024.

    • APA

      Avila, T. C., Reginato, M. M., Di Vitta, C., Ducati, L. C., Andrade, L. H., & Marzorati, L. (2016). On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds. Tetrahedrom Letters, 57, 2152-2157. doi:10.1016/j.tetlet.2016.03.109

    • NLM

      Avila TC, Reginato MM, Di Vitta C, Ducati LC, Andrade LH, Marzorati L. On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds [Internet]. Tetrahedrom Letters. 2016 ; 57 2152-2157.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2016.03.109

    • Vancouver

      Avila TC, Reginato MM, Di Vitta C, Ducati LC, Andrade LH, Marzorati L. On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds [Internet]. Tetrahedrom Letters. 2016 ; 57 2152-2157.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2016.03.109

  • Artigo de periodico

    Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems (2015)

    khalid, Muhammad; Souza Junior, Sergio Pereira de; Ciscato, Luiz Francisco Monteiro Leite; Bartoloni, Fernando Heering; Baader, Wilhelm Josef

    Source: Photochemical & Photobiological Sciences. Unidade: IQ

    Subjects: BIOLUMINESCÊNCIA, QUÍMICA ORGÂNICA

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      KHALID, Muhammad et al. Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems. Photochemical & Photobiological Sciences, v. 14, n. 7, p. 1296-1305, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5pp00152h. Acesso em: 31 jul. 2024.

    • APA

      khalid, M., Souza Junior, S. P. de, Ciscato, L. F. M. L., Bartoloni, F. H., & Baader, W. J. (2015). Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems. Photochemical & Photobiological Sciences, 14( 7), 1296-1305. doi:10.1039/c5pp00152h

    • NLM

      khalid M, Souza Junior SP de, Ciscato LFML, Bartoloni FH, Baader WJ. Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems [Internet]. Photochemical & Photobiological Sciences. 2015 ; 14( 7): 1296-1305.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1039/c5pp00152h

    • Vancouver

      khalid M, Souza Junior SP de, Ciscato LFML, Bartoloni FH, Baader WJ. Solvent viscosity influence on the chemiexcitation efficiency of inter and intramolecular chemiluminescence systems [Internet]. Photochemical & Photobiological Sciences. 2015 ; 14( 7): 1296-1305.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1039/c5pp00152h

  • Artigo de periodico

    Electrophilic alkynylation of ketones using hypervalent iodine (2014)

    Utaka, Aline; Cavalcanti, Livia N; Silva Junior, Luiz Fernando da

    Source: Chemical Communications. Unidade: IQ

    Subjects: COMPOSTOS ORGÂNICOS, QUÍMICA ORGÂNICA

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      UTAKA, Aline e CAVALCANTI, Livia N e SILVA JUNIOR, Luiz Fernando da. Electrophilic alkynylation of ketones using hypervalent iodine. Chemical Communications, v. 50, n. 29, p. 3810-3813, 2014Tradução . . Disponível em: https://doi.org/10.1039/c4cc00608a. Acesso em: 31 jul. 2024.

    • APA

      Utaka, A., Cavalcanti, L. N., & Silva Junior, L. F. da. (2014). Electrophilic alkynylation of ketones using hypervalent iodine. Chemical Communications, 50( 29), 3810-3813. doi:10.1039/c4cc00608a

    • NLM

      Utaka A, Cavalcanti LN, Silva Junior LF da. Electrophilic alkynylation of ketones using hypervalent iodine [Internet]. Chemical Communications. 2014 ; 50( 29): 3810-3813.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1039/c4cc00608a

    • Vancouver

      Utaka A, Cavalcanti LN, Silva Junior LF da. Electrophilic alkynylation of ketones using hypervalent iodine [Internet]. Chemical Communications. 2014 ; 50( 29): 3810-3813.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1039/c4cc00608a

  • Artigo de periodico

    On the thermal pummerer rearrangement of substituted sulfoxides (2014)

    Marzorati, Liliana ; Yoshikawa, Eduardo Kunio Chinone; Braga, Ataualpa Albert Carmo ; Di Vitta, Cláudio

    Source: Journal of Sulfur Chemistry. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      MARZORATI, Liliana et al. On the thermal pummerer rearrangement of substituted sulfoxides. Journal of Sulfur Chemistry, v. 35, n. 3, p. 248-260, 2014Tradução . . Disponível em: https://doi.org/10.1080/17415993.2013.853066. Acesso em: 31 jul. 2024.

    • APA

      Marzorati, L., Yoshikawa, E. K. C., Braga, A. A. C., & Di Vitta, C. (2014). On the thermal pummerer rearrangement of substituted sulfoxides. Journal of Sulfur Chemistry, 35( 3), 248-260. doi:10.1080/17415993.2013.853066

    • NLM

      Marzorati L, Yoshikawa EKC, Braga AAC, Di Vitta C. On the thermal pummerer rearrangement of substituted sulfoxides [Internet]. Journal of Sulfur Chemistry. 2014 ; 35( 3): 248-260.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1080/17415993.2013.853066

    • Vancouver

      Marzorati L, Yoshikawa EKC, Braga AAC, Di Vitta C. On the thermal pummerer rearrangement of substituted sulfoxides [Internet]. Journal of Sulfur Chemistry. 2014 ; 35( 3): 248-260.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1080/17415993.2013.853066

  • Artigo de periodico

    Kinetics and mechanism of imidazole-catalyzed acylation of cellulose in LiCl/N,N-dimethylacetamide (2013)

    Nawaz, Haq; Pires, Paulo Augusto Rodrigues; El Seoud, Omar A

    Source: Carbohydrate Polymers. Unidade: IQ

    Subjects: CELULOSE, QUÍMICA ORGÂNICA

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    • ABNT

      NAWAZ, Haq e PIRES, Paulo Augusto Rodrigues e EL SEOUD, Omar A. Kinetics and mechanism of imidazole-catalyzed acylation of cellulose in LiCl/N,N-dimethylacetamide. Carbohydrate Polymers, v. 92, n. 2, p. 997-1005, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.carbpol.2012.10.009. Acesso em: 31 jul. 2024.

    • APA

      Nawaz, H., Pires, P. A. R., & El Seoud, O. A. (2013). Kinetics and mechanism of imidazole-catalyzed acylation of cellulose in LiCl/N,N-dimethylacetamide. Carbohydrate Polymers, 92( 2), 997-1005. doi:10.1016/j.carbpol.2012.10.009

    • NLM

      Nawaz H, Pires PAR, El Seoud OA. Kinetics and mechanism of imidazole-catalyzed acylation of cellulose in LiCl/N,N-dimethylacetamide [Internet]. Carbohydrate Polymers. 2013 ; 92( 2): 997-1005.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.carbpol.2012.10.009

    • Vancouver

      Nawaz H, Pires PAR, El Seoud OA. Kinetics and mechanism of imidazole-catalyzed acylation of cellulose in LiCl/N,N-dimethylacetamide [Internet]. Carbohydrate Polymers. 2013 ; 92( 2): 997-1005.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.carbpol.2012.10.009

  • Artigo de periodico

    Solvatochromism of 2-(N,N-dimethylamino)-7-nitrofluorene and the natural dye 'beta'-carotene: application for the determination of solvent dipolarity and polarizability (2013)

    Pires, Paulo A. R.; Imran, Muhammad; Loffredo, Carina; Donate, Paulo Marcos; Previdi, Daniel; El Seoud, Omar A

    Source: Journal of Physical Organic Chemistry. Unidades: FFCLRP, IQ

    Subjects: SOLVENTE, QUÍMICA ORGÂNICA, FÍSICA

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    • ABNT

      PIRES, Paulo A. R. et al. Solvatochromism of 2-(N,N-dimethylamino)-7-nitrofluorene and the natural dye 'beta'-carotene: application for the determination of solvent dipolarity and polarizability. Journal of Physical Organic Chemistry, v. 26, n. 3, p. 280-285, 2013Tradução . . Disponível em: https://doi.org/10.1002/poc.3083. Acesso em: 31 jul. 2024.

    • APA

      Pires, P. A. R., Imran, M., Loffredo, C., Donate, P. M., Previdi, D., & El Seoud, O. A. (2013). Solvatochromism of 2-(N,N-dimethylamino)-7-nitrofluorene and the natural dye 'beta'-carotene: application for the determination of solvent dipolarity and polarizability. Journal of Physical Organic Chemistry, 26( 3), 280-285. doi:10.1002/poc.3083

    • NLM

      Pires PAR, Imran M, Loffredo C, Donate PM, Previdi D, El Seoud OA. Solvatochromism of 2-(N,N-dimethylamino)-7-nitrofluorene and the natural dye 'beta'-carotene: application for the determination of solvent dipolarity and polarizability [Internet]. Journal of Physical Organic Chemistry. 2013 ; 26( 3): 280-285.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1002/poc.3083

    • Vancouver

      Pires PAR, Imran M, Loffredo C, Donate PM, Previdi D, El Seoud OA. Solvatochromism of 2-(N,N-dimethylamino)-7-nitrofluorene and the natural dye 'beta'-carotene: application for the determination of solvent dipolarity and polarizability [Internet]. Journal of Physical Organic Chemistry. 2013 ; 26( 3): 280-285.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1002/poc.3083

  • Artigo de periodico

    VCD to determine absolute configuration of natural product molecules: secolignans from Peperomia blanda (2012)

    Felippe, Lidiane Gaspareto; Batista Junior, João Marcos; Baldoqui, Debora Cristina; Nascimento, Isabele R; Kato, Massuo Jorge ; He, Yanan; Nafie, Laurence A; Furlan, Maysa

    Source: Organic & Biomolecular Chemistry. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      FELIPPE, Lidiane Gaspareto et al. VCD to determine absolute configuration of natural product molecules: secolignans from Peperomia blanda. Organic & Biomolecular Chemistry, v. 10, n. 21, p. 4208-4214, 2012Tradução . . Disponível em: https://doi.org/10.1039/c2ob25109d. Acesso em: 31 jul. 2024.

    • APA

      Felippe, L. G., Batista Junior, J. M., Baldoqui, D. C., Nascimento, I. R., Kato, M. J., He, Y., et al. (2012). VCD to determine absolute configuration of natural product molecules: secolignans from Peperomia blanda. Organic & Biomolecular Chemistry, 10( 21), 4208-4214. doi:10.1039/c2ob25109d

    • NLM

      Felippe LG, Batista Junior JM, Baldoqui DC, Nascimento IR, Kato MJ, He Y, Nafie LA, Furlan M. VCD to determine absolute configuration of natural product molecules: secolignans from Peperomia blanda [Internet]. Organic & Biomolecular Chemistry. 2012 ; 10( 21): 4208-4214.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1039/c2ob25109d

    • Vancouver

      Felippe LG, Batista Junior JM, Baldoqui DC, Nascimento IR, Kato MJ, He Y, Nafie LA, Furlan M. VCD to determine absolute configuration of natural product molecules: secolignans from Peperomia blanda [Internet]. Organic & Biomolecular Chemistry. 2012 ; 10( 21): 4208-4214.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1039/c2ob25109d

  • Artigo de periodico

    Tellurium in organic synthesis: a general approach to buteno- and butanolides (2012)

    Ferrarini, Renan dos Santos; Santos, Alcindo Aparecido dos ; Comasseto, João Valdir

    Source: Tetrahedron. Unidade: IQ

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA

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      FERRARINI, Renan dos Santos e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. Tellurium in organic synthesis: a general approach to buteno- and butanolides. Tetrahedron, v. 68, n. 40, p. 10601-10610, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2012.09.074. Acesso em: 31 jul. 2024.

    • APA

      Ferrarini, R. dos S., Santos, A. A. dos, & Comasseto, J. V. (2012). Tellurium in organic synthesis: a general approach to buteno- and butanolides. Tetrahedron, 68( 40), 10601-10610. doi:10.1016/j.tet.2012.09.074

    • NLM

      Ferrarini R dos S, Santos AA dos, Comasseto JV. Tellurium in organic synthesis: a general approach to buteno- and butanolides [Internet]. Tetrahedron. 2012 ; 68( 40): 10601-10610.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.tet.2012.09.074

    • Vancouver

      Ferrarini R dos S, Santos AA dos, Comasseto JV. Tellurium in organic synthesis: a general approach to buteno- and butanolides [Internet]. Tetrahedron. 2012 ; 68( 40): 10601-10610.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.tet.2012.09.074

  • Artigo de periodico

    Kinetic resolution of α-bromophenylacetamides using quinine or Cinchona alkaloid salts (2012)

    Marzorati, Liliana ; Fejfar, José Luiz; Tormena, Cláudio Francisco; Di Vitta, Cláudio

    Source: Tetrahedron: Asymmetry. Unidade: IQ

    Subjects: ALCALOIDES, QUÍMICA ORGÂNICA

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    • ABNT

      MARZORATI, Liliana et al. Kinetic resolution of α-bromophenylacetamides using quinine or Cinchona alkaloid salts. Tetrahedron: Asymmetry, v. 23, n. 10, p. 748-753, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2012.05.009. Acesso em: 31 jul. 2024.

    • APA

      Marzorati, L., Fejfar, J. L., Tormena, C. F., & Di Vitta, C. (2012). Kinetic resolution of α-bromophenylacetamides using quinine or Cinchona alkaloid salts. Tetrahedron: Asymmetry, 23( 10), 748-753. doi:10.1016/j.tetasy.2012.05.009

    • NLM

      Marzorati L, Fejfar JL, Tormena CF, Di Vitta C. Kinetic resolution of α-bromophenylacetamides using quinine or Cinchona alkaloid salts [Internet]. Tetrahedron: Asymmetry. 2012 ; 23( 10): 748-753.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.tetasy.2012.05.009

    • Vancouver

      Marzorati L, Fejfar JL, Tormena CF, Di Vitta C. Kinetic resolution of α-bromophenylacetamides using quinine or Cinchona alkaloid salts [Internet]. Tetrahedron: Asymmetry. 2012 ; 23( 10): 748-753.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.tetasy.2012.05.009

  • Artigo de periodico

    Hypervalent iodine reagents in the total synthesis of natural products (2011)

    Silva Junior, Luiz Fernando da; Olofsson, Berit

    Source: Natural Product Reports. Unidade: IQ

    Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA

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    • ABNT

      SILVA JUNIOR, Luiz Fernando da e OLOFSSON, Berit. Hypervalent iodine reagents in the total synthesis of natural products. Natural Product Reports, v. 28, n. 10, p. 1722-1754, 2011Tradução . . Disponível em: https://doi.org/10.1039/c1np00028d. Acesso em: 31 jul. 2024.

    • APA

      Silva Junior, L. F. da, & Olofsson, B. (2011). Hypervalent iodine reagents in the total synthesis of natural products. Natural Product Reports, 28( 10), 1722-1754. doi:10.1039/c1np00028d

    • NLM

      Silva Junior LF da, Olofsson B. Hypervalent iodine reagents in the total synthesis of natural products [Internet]. Natural Product Reports. 2011 ; 28( 10): 1722-1754.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1039/c1np00028d

    • Vancouver

      Silva Junior LF da, Olofsson B. Hypervalent iodine reagents in the total synthesis of natural products [Internet]. Natural Product Reports. 2011 ; 28( 10): 1722-1754.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1039/c1np00028d

  • Artigo de periodico

    Hypervalent organochalcogenanes as inhibitors of protein tyrosine phosphatases (2011)

    Piovan, Leandro; Wu, Li; Zhang, Zhong Yin; Andrade, Leandro Helgueira

    Source: Organic & Biomolecular Chemistry. Unidade: IQ

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA

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    • ABNT

      PIOVAN, Leandro et al. Hypervalent organochalcogenanes as inhibitors of protein tyrosine phosphatases. Organic & Biomolecular Chemistry, v. 9, n. 5, p. 1347-1351, 2011Tradução . . Disponível em: https://doi.org/10.1039/c0ob01050b. Acesso em: 31 jul. 2024.

    • APA

      Piovan, L., Wu, L., Zhang, Z. Y., & Andrade, L. H. (2011). Hypervalent organochalcogenanes as inhibitors of protein tyrosine phosphatases. Organic & Biomolecular Chemistry, 9( 5), 1347-1351. doi:10.1039/c0ob01050b

    • NLM

      Piovan L, Wu L, Zhang ZY, Andrade LH. Hypervalent organochalcogenanes as inhibitors of protein tyrosine phosphatases [Internet]. Organic & Biomolecular Chemistry. 2011 ; 9( 5): 1347-1351.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1039/c0ob01050b

    • Vancouver

      Piovan L, Wu L, Zhang ZY, Andrade LH. Hypervalent organochalcogenanes as inhibitors of protein tyrosine phosphatases [Internet]. Organic & Biomolecular Chemistry. 2011 ; 9( 5): 1347-1351.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1039/c0ob01050b

  • Artigo de periodico

    Absolute configuration reassignment of two chromanes from Peperomia obtusifolia (Piperaceae) using VCD and DFT calculations (2010)

    Batista Junior, João Marcos; Batista, Andrea N. L; Rinaldo, Daniel; Vilegas, Wagner; Cass, Quezia Bezerra; Bolzani, Vanderlan da Silva; Kato, Massuo Jorge ; López, Silvia Noelí; Furlan, Maysa; Nafie, Laurence A

    Source: Tetrahedron: Asymmetry. Unidade: IQ

    Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA

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    • ABNT

      BATISTA JUNIOR, João Marcos et al. Absolute configuration reassignment of two chromanes from Peperomia obtusifolia (Piperaceae) using VCD and DFT calculations. Tetrahedron: Asymmetry, v. 21, n. 19, p. 2402-2407, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2010.09.004. Acesso em: 31 jul. 2024.

    • APA

      Batista Junior, J. M., Batista, A. N. L., Rinaldo, D., Vilegas, W., Cass, Q. B., Bolzani, V. da S., et al. (2010). Absolute configuration reassignment of two chromanes from Peperomia obtusifolia (Piperaceae) using VCD and DFT calculations. Tetrahedron: Asymmetry, 21( 19), 2402-2407. doi:10.1016/j.tetasy.2010.09.004

    • NLM

      Batista Junior JM, Batista ANL, Rinaldo D, Vilegas W, Cass QB, Bolzani V da S, Kato MJ, López SN, Furlan M, Nafie LA. Absolute configuration reassignment of two chromanes from Peperomia obtusifolia (Piperaceae) using VCD and DFT calculations [Internet]. Tetrahedron: Asymmetry. 2010 ; 21( 19): 2402-2407.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.tetasy.2010.09.004

    • Vancouver

      Batista Junior JM, Batista ANL, Rinaldo D, Vilegas W, Cass QB, Bolzani V da S, Kato MJ, López SN, Furlan M, Nafie LA. Absolute configuration reassignment of two chromanes from Peperomia obtusifolia (Piperaceae) using VCD and DFT calculations [Internet]. Tetrahedron: Asymmetry. 2010 ; 21( 19): 2402-2407.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.tetasy.2010.09.004

  • Artigo de periodico

    Electrical and optical properties of poly(2-dodecanoylsulfanyl-p-phenylenevnylene) and its application in electroluminescent devices (2010)

    Nodari, Fernanda Maria; Patyk, Rodolfo Luiz; Roman, Lucimara Stolz; Benvenho, Adriano Reinaldo Viçoto; Hümmelgen, Ivo Alexandre; Yoshikawa, Eduardo Kunio Chinone; Gruber, Jonas

    Source: Journal of Materials Science: Materials in Electronics. Unidade: IQ

    Subjects: POLÍMEROS (QUÍMICA ORGÂNICA), QUÍMICA ORGÂNICA

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    • ABNT

      NODARI, Fernanda Maria et al. Electrical and optical properties of poly(2-dodecanoylsulfanyl-p-phenylenevnylene) and its application in electroluminescent devices. Journal of Materials Science: Materials in Electronics, v. 21, n. 12, p. 1235-1239, 2010Tradução . . Disponível em: https://doi.org/10.1007/s10854-009-0052-8. Acesso em: 31 jul. 2024.

    • APA

      Nodari, F. M., Patyk, R. L., Roman, L. S., Benvenho, A. R. V., Hümmelgen, I. A., Yoshikawa, E. K. C., & Gruber, J. (2010). Electrical and optical properties of poly(2-dodecanoylsulfanyl-p-phenylenevnylene) and its application in electroluminescent devices. Journal of Materials Science: Materials in Electronics, 21( 12), 1235-1239. doi:10.1007/s10854-009-0052-8

    • NLM

      Nodari FM, Patyk RL, Roman LS, Benvenho ARV, Hümmelgen IA, Yoshikawa EKC, Gruber J. Electrical and optical properties of poly(2-dodecanoylsulfanyl-p-phenylenevnylene) and its application in electroluminescent devices [Internet]. Journal of Materials Science: Materials in Electronics. 2010 ; 21( 12): 1235-1239.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1007/s10854-009-0052-8

    • Vancouver

      Nodari FM, Patyk RL, Roman LS, Benvenho ARV, Hümmelgen IA, Yoshikawa EKC, Gruber J. Electrical and optical properties of poly(2-dodecanoylsulfanyl-p-phenylenevnylene) and its application in electroluminescent devices [Internet]. Journal of Materials Science: Materials in Electronics. 2010 ; 21( 12): 1235-1239.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1007/s10854-009-0052-8

  • Artigo de periodico

    The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction (2009)

    Silva, Márcio S.; Santos, Alcindo Aparecido dos ; Comasseto, João Valdir

    Source: Tetrahedron Letters. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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    • ABNT

      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: 31 jul. 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 jul. 31 ] 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 jul. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2009.09.023

  • Artigo de periodico

    Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent (2009)

    Andrade, Leandro Helgueira ; Piovan, Leandro; Pasquini, Mônica D`Arcadia

    Source: Tetrahedron Asymmetry. Unidade: IQ

    Subjects: ASPERGILLUS, QUÍMICA ORGÂNICA

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    • ABNT

      ANDRADE, Leandro Helgueira e PIOVAN, Leandro e PASQUINI, Mônica D`Arcadia. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, v. 20, n. 13, p. 1521-1525, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.05.033. Acesso em: 31 jul. 2024.

    • APA

      Andrade, L. H., Piovan, L., & Pasquini, M. D. `A. (2009). Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, 20( 13), 1521-1525. doi:10.1016/j.tetasy.2009.05.033

    • NLM

      Andrade LH, Piovan L, Pasquini MD`A. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent [Internet]. Tetrahedron Asymmetry. 2009 ; 20( 13): 1521-1525.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033

    • Vancouver

      Andrade LH, Piovan L, Pasquini MD`A. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent [Internet]. Tetrahedron Asymmetry. 2009 ; 20( 13): 1521-1525.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033

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