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  • Artigo de periodico

    Synthesis of a hydrophilic and non-ionic anthracene derivative, the N,N '-di-(2,3-dihydroxypropyl)-9,10-anthracenedipropanamide as a chemical trap for singlet molecular oxygen detection in biological systems (2006)

    Martinez, Glaucia Regina; Garcia, Flávia; Catalani, Luiz Henrique ; Cadet, Jean; Oliveira, Maurício C. B. de; Ronsein, Graziella Eliza ; Miyamoto, Sayuri ; Medeiros, Marisa Helena Gennari de ; Di Mascio, Paolo

    Source: Tetrahedron. Unidade: IQ

    Subjects: BIOQUÍMICA, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA (MÉTODOS)

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    • ABNT

      MARTINEZ, Glaucia Regina et al. Synthesis of a hydrophilic and non-ionic anthracene derivative, the N,N '-di-(2,3-dihydroxypropyl)-9,10-anthracenedipropanamide as a chemical trap for singlet molecular oxygen detection in biological systems. Tetrahedron, v. 62, n. 46, p. 10762-10770, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2006.08.094. Acesso em: 18 set. 2024.

    • APA

      Martinez, G. R., Garcia, F., Catalani, L. H., Cadet, J., Oliveira, M. C. B. de, Ronsein, G. E., et al. (2006). Synthesis of a hydrophilic and non-ionic anthracene derivative, the N,N '-di-(2,3-dihydroxypropyl)-9,10-anthracenedipropanamide as a chemical trap for singlet molecular oxygen detection in biological systems. Tetrahedron, 62( 46), 10762-10770. doi:10.1016/j.tet.2006.08.094

    • NLM

      Martinez GR, Garcia F, Catalani LH, Cadet J, Oliveira MCB de, Ronsein GE, Miyamoto S, Medeiros MHG de, Di Mascio P. Synthesis of a hydrophilic and non-ionic anthracene derivative, the N,N '-di-(2,3-dihydroxypropyl)-9,10-anthracenedipropanamide as a chemical trap for singlet molecular oxygen detection in biological systems [Internet]. Tetrahedron. 2006 ; 62( 46): 10762-10770.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2006.08.094

    • Vancouver

      Martinez GR, Garcia F, Catalani LH, Cadet J, Oliveira MCB de, Ronsein GE, Miyamoto S, Medeiros MHG de, Di Mascio P. Synthesis of a hydrophilic and non-ionic anthracene derivative, the N,N '-di-(2,3-dihydroxypropyl)-9,10-anthracenedipropanamide as a chemical trap for singlet molecular oxygen detection in biological systems [Internet]. Tetrahedron. 2006 ; 62( 46): 10762-10770.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2006.08.094

  • Artigo de periodico

    'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity (2006)

    Melo, Eduardo Borges de; Gomes, Adriane da Silveira; Carvalho, Ivone

    Source: Tetrahedron. Unidade: FCFRP

    Subjects: ENZIMAS GLICOLÍTICAS, INIBIDORES DE ENZIMAS

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    • ABNT

      MELO, Eduardo Borges de e GOMES, Adriane da Silveira e CARVALHO, Ivone. 'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron, v. 62, n. 44, p. 10277-10302, 2006Tradução . . Acesso em: 18 set. 2024.

    • APA

      Melo, E. B. de, Gomes, A. da S., & Carvalho, I. (2006). 'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron, 62( 44), 10277-10302.

    • NLM

      Melo EB de, Gomes A da S, Carvalho I. 'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron. 2006 ; 62( 44): 10277-10302.[citado 2024 set. 18 ]

    • Vancouver

      Melo EB de, Gomes A da S, Carvalho I. 'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron. 2006 ; 62( 44): 10277-10302.[citado 2024 set. 18 ]

  • Artigo de periodico

    Singlet oxygen oxidation of 2 '-deoxyguanosine. Formation and mechanistic insights (2006)

    Ravanat, Jean-Luc; Martinez, Glaucia Regina; Medeiros, Marisa Helena Gennari de ; Di Mascio, Paolo ; Cadet, Jean

    Source: Tetrahedron. Unidade: IQ

    Subjects: OXIDAÇÃO, BIOQUÍMICA

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    • ABNT

      RAVANAT, Jean-Luc et al. Singlet oxygen oxidation of 2 '-deoxyguanosine. Formation and mechanistic insights. Tetrahedron, v. 62, n. 46, p. 10709-10715, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2006.08.097. Acesso em: 18 set. 2024.

    • APA

      Ravanat, J. -L., Martinez, G. R., Medeiros, M. H. G. de, Di Mascio, P., & Cadet, J. (2006). Singlet oxygen oxidation of 2 '-deoxyguanosine. Formation and mechanistic insights. Tetrahedron, 62( 46), 10709-10715. doi:10.1016/j.tet.2006.08.097

    • NLM

      Ravanat J-L, Martinez GR, Medeiros MHG de, Di Mascio P, Cadet J. Singlet oxygen oxidation of 2 '-deoxyguanosine. Formation and mechanistic insights [Internet]. Tetrahedron. 2006 ; 62( 46): 10709-10715.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2006.08.097

    • Vancouver

      Ravanat J-L, Martinez GR, Medeiros MHG de, Di Mascio P, Cadet J. Singlet oxygen oxidation of 2 '-deoxyguanosine. Formation and mechanistic insights [Internet]. Tetrahedron. 2006 ; 62( 46): 10709-10715.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2006.08.097

  • Artigo de periodico

    An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins (2006)

    Nihei, Ken-ichi; Kato, Massuo Jorge ; Yamane, Tetsuo; Konno, Katsuhiro

    Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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    • ABNT

      NIHEI, Ken-ichi et al. An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins. Tetrahedron, v. 62, n. 35, p. 8335-8350, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2006.06.051. Acesso em: 18 set. 2024.

    • APA

      Nihei, K. -ichi, Kato, M. J., Yamane, T., & Konno, K. (2006). An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins. Tetrahedron, 62( 35), 8335-8350. doi:10.1016/j.tet.2006.06.051

    • NLM

      Nihei K-ichi, Kato MJ, Yamane T, Konno K. An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins [Internet]. Tetrahedron. 2006 ; 62( 35): 8335-8350.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2006.06.051

    • Vancouver

      Nihei K-ichi, Kato MJ, Yamane T, Konno K. An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins [Internet]. Tetrahedron. 2006 ; 62( 35): 8335-8350.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2006.06.051

  • Artigo de periodico

    Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts (2006)

    Cella, Rodrigo; Stefani, Hélio Alexandre

    Source: Tetrahedron. Unidade: FCF

    Subjects: ULTRASSONOGRAFIA, TELÚRIO, POTÁSSIO

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    • ABNT

      CELLA, Rodrigo e STEFANI, Hélio Alexandre. Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts. Tetrahedron, v. 62, n. 24, p. 5656-5662, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2006.03.090. Acesso em: 18 set. 2024.

    • APA

      Cella, R., & Stefani, H. A. (2006). Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts. Tetrahedron, 62( 24), 5656-5662. doi:10.1016/j.tet.2006.03.090

    • NLM

      Cella R, Stefani HA. Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts [Internet]. Tetrahedron. 2006 ; 62( 24): 5656-5662.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2006.03.090

    • Vancouver

      Cella R, Stefani HA. Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts [Internet]. Tetrahedron. 2006 ; 62( 24): 5656-5662.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2006.03.090

  • Artigo de periodico

    Calculated NMR as a tool for structural elucidation of jungianol and mutisianthol (2005)

    Silva, Gil Valdo José da; Cunha Neto, Álvaro

    Source: Tetrahedron. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      SILVA, Gil Valdo José da e CUNHA NETO, Álvaro. Calculated NMR as a tool for structural elucidation of jungianol and mutisianthol. Tetrahedron, v. 61, p. 7763-7767, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2005.05.101. Acesso em: 18 set. 2024.

    • APA

      Silva, G. V. J. da, & Cunha Neto, Á. (2005). Calculated NMR as a tool for structural elucidation of jungianol and mutisianthol. Tetrahedron, 61, 7763-7767. doi:10.1016/j.tet.2005.05.101

    • NLM

      Silva GVJ da, Cunha Neto Á. Calculated NMR as a tool for structural elucidation of jungianol and mutisianthol [Internet]. Tetrahedron. 2005 ; 61 7763-7767.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2005.05.101

    • Vancouver

      Silva GVJ da, Cunha Neto Á. Calculated NMR as a tool for structural elucidation of jungianol and mutisianthol [Internet]. Tetrahedron. 2005 ; 61 7763-7767.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2005.05.101

  • Artigo de periodico

    Regio- and stereoselective synthesis of Z-vinylic tellurides from propargylic alcohols: a route to chiral Z-enynes (2005)

    Raminelli, Cristiano; Silva, Nathalia C. da; Dos Santos, Alcindo Aparecido; Porto, Andre Luiz Meleiro ; Andrade, Leandro Helgueira ; Comasseto, João Valdir

    Source: Tetrahedron. Unidade: IQ

    Subjects: REAGENTES ORGÂNICOS, QUÍMICA ORGÂNICA

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    • ABNT

      RAMINELLI, Cristiano et al. Regio- and stereoselective synthesis of Z-vinylic tellurides from propargylic alcohols: a route to chiral Z-enynes. Tetrahedron, v. 61, n. 2, p. 409-415, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2004.10.087. Acesso em: 18 set. 2024.

    • APA

      Raminelli, C., Silva, N. C. da, Dos Santos, A. A., Porto, A. L. M., Andrade, L. H., & Comasseto, J. V. (2005). Regio- and stereoselective synthesis of Z-vinylic tellurides from propargylic alcohols: a route to chiral Z-enynes. Tetrahedron, 61( 2), 409-415. doi:10.1016/j.tet.2004.10.087

    • NLM

      Raminelli C, Silva NC da, Dos Santos AA, Porto ALM, Andrade LH, Comasseto JV. Regio- and stereoselective synthesis of Z-vinylic tellurides from propargylic alcohols: a route to chiral Z-enynes [Internet]. Tetrahedron. 2005 ; 61( 2): 409-415.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2004.10.087

    • Vancouver

      Raminelli C, Silva NC da, Dos Santos AA, Porto ALM, Andrade LH, Comasseto JV. Regio- and stereoselective synthesis of Z-vinylic tellurides from propargylic alcohols: a route to chiral Z-enynes [Internet]. Tetrahedron. 2005 ; 61( 2): 409-415.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2004.10.087

  • Artigo de periodico

    Advances in organic tellurium chemistry (2005)

    Petragnani, Nicola; Stefani, Hélio Alexandre

    Source: Tetrahedron. Unidades: IQ, FCF

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA

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    • ABNT

      PETRAGNANI, Nicola e STEFANI, Hélio Alexandre. Advances in organic tellurium chemistry. Tetrahedron, v. 61, n. 7, p. 1613-1679, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2004.11.076. Acesso em: 18 set. 2024.

    • APA

      Petragnani, N., & Stefani, H. A. (2005). Advances in organic tellurium chemistry. Tetrahedron, 61( 7), 1613-1679. doi:10.1016/j.tet.2004.11.076

    • NLM

      Petragnani N, Stefani HA. Advances in organic tellurium chemistry [Internet]. Tetrahedron. 2005 ; 61( 7): 1613-1679.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2004.11.076

    • Vancouver

      Petragnani N, Stefani HA. Advances in organic tellurium chemistry [Internet]. Tetrahedron. 2005 ; 61( 7): 1613-1679.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2004.11.076

  • Artigo de periodico

    Diastereoselective synthesis of 'alpha','beta'-unsaturated systems (2005)

    Castelani, Priscila; Comasseto, João Valdir

    Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, TELÚRIO, REAGENTES ORGÂNICOS

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    • ABNT

      CASTELANI, Priscila e COMASSETO, João Valdir. Diastereoselective synthesis of 'alpha','beta'-unsaturated systems. Tetrahedron, v. 61, n. 9, p. 2319-2326, 2005Tradução . . Acesso em: 18 set. 2024.

    • APA

      Castelani, P., & Comasseto, J. V. (2005). Diastereoselective synthesis of 'alpha','beta'-unsaturated systems. Tetrahedron, 61( 9), 2319-2326.

    • NLM

      Castelani P, Comasseto JV. Diastereoselective synthesis of 'alpha','beta'-unsaturated systems. Tetrahedron. 2005 ; 61( 9): 2319-2326.[citado 2024 set. 18 ]

    • Vancouver

      Castelani P, Comasseto JV. Diastereoselective synthesis of 'alpha','beta'-unsaturated systems. Tetrahedron. 2005 ; 61( 9): 2319-2326.[citado 2024 set. 18 ]

  • Artigo de periodico

    Chemoselective reduction of beta-butyltellanyl 'alpha','beta'-unsaturated carbonyl compounds to allylic alcohols (2005)

    Dos Santos, Alcindo Aparecido; Castelani, Priscila; Bassora, Bruno Karaski; Fogo Junior, José Carlos; Costa, Carlos Eduardo da; Comasseto, João Valdir

    Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, REAGENTES ORGÂNICOS

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    • ABNT

      DOS SANTOS, Alcindo Aparecido et al. Chemoselective reduction of beta-butyltellanyl 'alpha','beta'-unsaturated carbonyl compounds to allylic alcohols. Tetrahedron, v. 61, n. 38, p. 9173-9179, 2005Tradução . . Acesso em: 18 set. 2024.

    • APA

      Dos Santos, A. A., Castelani, P., Bassora, B. K., Fogo Junior, J. C., Costa, C. E. da, & Comasseto, J. V. (2005). Chemoselective reduction of beta-butyltellanyl 'alpha','beta'-unsaturated carbonyl compounds to allylic alcohols. Tetrahedron, 61( 38), 9173-9179.

    • NLM

      Dos Santos AA, Castelani P, Bassora BK, Fogo Junior JC, Costa CE da, Comasseto JV. Chemoselective reduction of beta-butyltellanyl 'alpha','beta'-unsaturated carbonyl compounds to allylic alcohols. Tetrahedron. 2005 ; 61( 38): 9173-9179.[citado 2024 set. 18 ]

    • Vancouver

      Dos Santos AA, Castelani P, Bassora BK, Fogo Junior JC, Costa CE da, Comasseto JV. Chemoselective reduction of beta-butyltellanyl 'alpha','beta'-unsaturated carbonyl compounds to allylic alcohols. Tetrahedron. 2005 ; 61( 38): 9173-9179.[citado 2024 set. 18 ]

  • Artigo de periodico

    Photophysical and electrochemical properties of 'pi'-extended molecular 2,1,3-benzothiadiazoles (2005)

    DaSilveira Neto, Brenno; Lopes, Aline Sant'Ana; Ebeling, Gunter; Gonçalves, Reinaldo S.; Costa, Valentim Emilio Uberti; Quina, Frank Herbert ; Dupont, Jairton

    Source: Tetrahedron. Unidade: IQ

    Subjects: REAÇÕES QUÍMICAS, FOTOQUÍMICA ORGÂNICA (PROPRIEDADES), FOTOLUMINESCÊNCIA (PROPRIEDADES), ELETROQUÍMICA (PROPRIEDADES)

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    • ABNT

      DASILVEIRA NETO, Brenno et al. Photophysical and electrochemical properties of 'pi'-extended molecular 2,1,3-benzothiadiazoles. Tetrahedron, v. 61, n. 46, p. 10975-10982, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2005.08.093. Acesso em: 18 set. 2024.

    • APA

      DaSilveira Neto, B., Lopes, A. S. 'A., Ebeling, G., Gonçalves, R. S., Costa, V. E. U., Quina, F. H., & Dupont, J. (2005). Photophysical and electrochemical properties of 'pi'-extended molecular 2,1,3-benzothiadiazoles. Tetrahedron, 61( 46), 10975-10982. doi:10.1016/j.tet.2005.08.093

    • NLM

      DaSilveira Neto B, Lopes AS'A, Ebeling G, Gonçalves RS, Costa VEU, Quina FH, Dupont J. Photophysical and electrochemical properties of 'pi'-extended molecular 2,1,3-benzothiadiazoles [Internet]. Tetrahedron. 2005 ; 61( 46): 10975-10982.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2005.08.093

    • Vancouver

      DaSilveira Neto B, Lopes AS'A, Ebeling G, Gonçalves RS, Costa VEU, Quina FH, Dupont J. Photophysical and electrochemical properties of 'pi'-extended molecular 2,1,3-benzothiadiazoles [Internet]. Tetrahedron. 2005 ; 61( 46): 10975-10982.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2005.08.093

  • Artigo de periodico

    NMR structure determination of (11E)- trinervita-1(14),2,11-triene, a new diterpene from sexual glands of termite (2005)

    Budesinsky, Miklos; Valterová, Irena; Sémon, Etienne; Cancello, Eliana Marques; Bordereau, Christian

    Source: Tetrahedron. Unidade: MZ

    Assunto: ISOPTERA

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    • ABNT

      BUDESINSKY, Miklos et al. NMR structure determination of (11E)- trinervita-1(14),2,11-triene, a new diterpene from sexual glands of termite. Tetrahedron, v. 61, n. 45, p. 10699-10704, 2005Tradução . . Acesso em: 18 set. 2024.

    • APA

      Budesinsky, M., Valterová, I., Sémon, E., Cancello, E. M., & Bordereau, C. (2005). NMR structure determination of (11E)- trinervita-1(14),2,11-triene, a new diterpene from sexual glands of termite. Tetrahedron, 61( 45), 10699-10704.

    • NLM

      Budesinsky M, Valterová I, Sémon E, Cancello EM, Bordereau C. NMR structure determination of (11E)- trinervita-1(14),2,11-triene, a new diterpene from sexual glands of termite. Tetrahedron. 2005 ; 61( 45): 10699-10704.[citado 2024 set. 18 ]

    • Vancouver

      Budesinsky M, Valterová I, Sémon E, Cancello EM, Bordereau C. NMR structure determination of (11E)- trinervita-1(14),2,11-triene, a new diterpene from sexual glands of termite. Tetrahedron. 2005 ; 61( 45): 10699-10704.[citado 2024 set. 18 ]

  • Artigo de periodico

    Racemization in stepwise solid-phase peptide synthesis at elevated temperatures (2004)

    Souza, Marcos P.; Tavares, Marina Franco Maggi ; Miranda, Maria Terêsa Machini de

    Source: Tetrahedron. Unidade: IQ

    Subjects: AMINOÁCIDOS, ESPECTROMETRIA DE MASSAS, PEPTÍDEOS (SÍNTESE), QUÍMICA ANALÍTICA, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, ELETROFORESE CAPILAR DE ZONA

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    • ABNT

      SOUZA, Marcos P. e TAVARES, Marina Franco Maggi e MIRANDA, Maria Terêsa Machini de. Racemization in stepwise solid-phase peptide synthesis at elevated temperatures. Tetrahedron, v. 60, n. 21, p. 4671-4681, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2004.03.070. Acesso em: 18 set. 2024.

    • APA

      Souza, M. P., Tavares, M. F. M., & Miranda, M. T. M. de. (2004). Racemization in stepwise solid-phase peptide synthesis at elevated temperatures. Tetrahedron, 60( 21), 4671-4681. doi:10.1016/j.tet.2004.03.070

    • NLM

      Souza MP, Tavares MFM, Miranda MTM de. Racemization in stepwise solid-phase peptide synthesis at elevated temperatures [Internet]. Tetrahedron. 2004 ; 60( 21): 4671-4681.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2004.03.070

    • Vancouver

      Souza MP, Tavares MFM, Miranda MTM de. Racemization in stepwise solid-phase peptide synthesis at elevated temperatures [Internet]. Tetrahedron. 2004 ; 60( 21): 4671-4681.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tet.2004.03.070

  • Artigo de periodico

    Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides (2003)

    Donate, Paulo Marcos; Frederico, Daniel; Silva, Rosangela da; Constantino, Maurício Gomes; Del Ponte, Gino; Bonatto, Pierina Sueli

    Source: Tetrahedron. Unidades: FFCLRP, FCFRP

    Assunto: FÁRMACOS (QUÍMICA)

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    • ABNT

      DONATE, Paulo Marcos et al. Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides. Tetrahedron, v. 14, p. 3253-3256, 2003Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2003.08.031. Acesso em: 18 set. 2024.

    • APA

      Donate, P. M., Frederico, D., Silva, R. da, Constantino, M. G., Del Ponte, G., & Bonatto, P. S. (2003). Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides. Tetrahedron, 14, 3253-3256. doi:10.1016/j.tetasy.2003.08.031

    • NLM

      Donate PM, Frederico D, Silva R da, Constantino MG, Del Ponte G, Bonatto PS. Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides [Internet]. Tetrahedron. 2003 ; 14 3253-3256.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tetasy.2003.08.031

    • Vancouver

      Donate PM, Frederico D, Silva R da, Constantino MG, Del Ponte G, Bonatto PS. Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides [Internet]. Tetrahedron. 2003 ; 14 3253-3256.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tetasy.2003.08.031

  • Artigo de periodico

    A diastereoselective total synthesis of the sesquiterpene (+or-)-mutisianthol (2003)

    Ferraz, Helena Maria Carvalho; Aguilar, Andrea Maria; Silva Jr., Luiz Fernando da

    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: 18 set. 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 set. 18 ] 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 set. 18 ] Available from: https://doi.org/10.1016/s0040-4020(03)00974-8

  • Artigo de periodico

    Clean and efficient microwave-solvent-free synthesis of 1-(2',4'-dichlorophenacyl) azoles (2003)

    Pérez, Eduardo R.; Loupy, André; Liagre, Marion; Plepis, Ana Maria de Guzzi ; Cordeiro, Paulo Jorge Marques

    Source: Tetrahedron. Unidade: IQSC

    Subjects: QUÍMICA, FUNGICIDAS

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    • ABNT

      PÉREZ, Eduardo R. et al. Clean and efficient microwave-solvent-free synthesis of 1-(2',4'-dichlorophenacyl) azoles. Tetrahedron, v. 59, p. 865-870, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(02)01622-8. Acesso em: 18 set. 2024.

    • APA

      Pérez, E. R., Loupy, A., Liagre, M., Plepis, A. M. de G., & Cordeiro, P. J. M. (2003). Clean and efficient microwave-solvent-free synthesis of 1-(2',4'-dichlorophenacyl) azoles. Tetrahedron, 59, 865-870. doi:10.1016/s0040-4020(02)01622-8

    • NLM

      Pérez ER, Loupy A, Liagre M, Plepis AM de G, Cordeiro PJM. Clean and efficient microwave-solvent-free synthesis of 1-(2',4'-dichlorophenacyl) azoles [Internet]. Tetrahedron. 2003 ; 59 865-870.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/s0040-4020(02)01622-8

    • Vancouver

      Pérez ER, Loupy A, Liagre M, Plepis AM de G, Cordeiro PJM. Clean and efficient microwave-solvent-free synthesis of 1-(2',4'-dichlorophenacyl) azoles [Internet]. Tetrahedron. 2003 ; 59 865-870.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/s0040-4020(02)01622-8

  • Artigo de periodico

    Construction of cyclopentyl units by ring contraction reactions (2002)

    Silva Jr., Luiz Fernando da

    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: 18 set. 2024.

    • APA

      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 set. 18 ] 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 set. 18 ] Available from: https://doi.org/10.1016/s0040-4020(02)00990-0

  • Artigo de periodico

    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 (2002)

    Alves, C. N.; Silva, Alberico Borges Ferreira da ; Martí, S.; Moliner, V.; Oliva, M.; Andrés, J.; Domingo, L. R.

    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: 18 set. 2024.

    • APA

      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 set. 18 ] 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 set. 18 ] Available from: https://doi.org/10.1016/s0040-4020(02)00072-8

  • Artigo de periodico

    A general method of synthesis of functionalized Z-vinylic tellurides starting from beta-dicarbonyl compounds (2002)

    Barrientos-Astigarraga, Rafael Eliseo; Castelani, Priscila; Sumida, Celso Y.; Zukerman-Schpector, Júlio; Comasseto, João Valdir

    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: 18 set. 2024.

    • APA

      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 set. 18 ] 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 set. 18 ] Available from: https://doi.org/10.1016/s0040-4020(01)01204-2

  • Artigo de periodico

    Thallium trinitrate-mediated ring contaction of 1,2-dihydronaphthalenes: an approach to the synthesis of indans (2001)

    Ferraz, Helena Maria Carvalho; Silva Junior, Luiz Fernando da; Vieira, Tiago O.

    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: 18 set. 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 set. 18 ] 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 set. 18 ] Available from: https://doi.org/10.1016/s0040-4020(00)01174-1

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