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Artigo de periodico
Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles (2019)
Balfour, Michael N; Schpector, Júlio Zukerman; Rodriguez, Maria Jose Davila; Reis, Joel Savi dos; Esteves, Carlos Henrique Alves; Stefani, Hélio Alexandre
Fonte: Synthetic Communications. Unidade: FCF
Assuntos: COMPOSTOS HETEROCÍCLICOS, SÍNTESE QUÍMICA
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ABNT
BALFOUR, Michael N et al. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles. Synthetic Communications, v. 49, n. 3, p. 351-358, 2019Tradução . . Disponível em: https://doi.org/10.1080/00397911.2018.1545032. Acesso em: 23 abr. 2024.
APA
Balfour, M. N., Schpector, J. Z., Rodriguez, M. J. D., Reis, J. S. dos, Esteves, C. H. A., & Stefani, H. A. (2019). Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles. Synthetic Communications, 49( 3), 351-358. doi:10.1080/00397911.2018.1545032
NLM
Balfour MN, Schpector JZ, Rodriguez MJD, Reis JS dos, Esteves CHA, Stefani HA. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles [Internet]. Synthetic Communications. 2019 ; 49( 3): 351-358.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1080/00397911.2018.1545032
Vancouver
Balfour MN, Schpector JZ, Rodriguez MJD, Reis JS dos, Esteves CHA, Stefani HA. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles [Internet]. Synthetic Communications. 2019 ; 49( 3): 351-358.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1080/00397911.2018.1545032
Artigo de periodico
Sonogashira cross-coupling in iodo-containing 2-aryloxazolines (2019)
Reis, Joel Savi dos; Caracelli, Ignez ; Schpector, Júlio Zukerman ; Stefani, Hélio Alexandre
Fonte: Synthetic Communications. Unidade: FCF
Assuntos: PALÁDIO, COMPOSTOS HETEROCÍCLICOS
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ABNT
REIS, Joel Savi dos et al. Sonogashira cross-coupling in iodo-containing 2-aryloxazolines. Synthetic Communications, v. 49, n. 10, p. 1252-1261, 2019Tradução . . Disponível em: https://doi.org/10.1080/00397911.2019.1595657. Acesso em: 23 abr. 2024.
APA
Reis, J. S. dos, Caracelli, I., Schpector, J. Z., & Stefani, H. A. (2019). Sonogashira cross-coupling in iodo-containing 2-aryloxazolines. Synthetic Communications, 49( 10), 1252-1261. doi:10.1080/00397911.2019.1595657
NLM
Reis JS dos, Caracelli I, Schpector JZ, Stefani HA. Sonogashira cross-coupling in iodo-containing 2-aryloxazolines [Internet]. Synthetic Communications. 2019 ; 49( 10): 1252-1261.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1080/00397911.2019.1595657
Vancouver
Reis JS dos, Caracelli I, Schpector JZ, Stefani HA. Sonogashira cross-coupling in iodo-containing 2-aryloxazolines [Internet]. Synthetic Communications. 2019 ; 49( 10): 1252-1261.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1080/00397911.2019.1595657
Artigo de periodico
Ultrasound-promoted environmentally friendly synthesis of 5-(3,3,3-trifluoro-2-oxopropylidene)pyrrolidin-2-ones (2015)
Franco, Maria Silvana Freire; Casagrande, Gleison Antônio; Raminelli, Cristiano; Moura, Sidnei; Rossatto, Marcelo; Quina, Frank Herbert ; Pereira, Claudio Martim Pereira de; Flores, Alex Fabiani Claro; Pizzuti, Lucas
Fonte: Synthetic Communications. Unidade: IQ
Assuntos: ULTRASSOM, SÍNTESE QUÍMICA
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ABNT
FRANCO, Maria Silvana Freire et al. Ultrasound-promoted environmentally friendly synthesis of 5-(3,3,3-trifluoro-2-oxopropylidene)pyrrolidin-2-ones. Synthetic Communications, v. 45, n. 6, p. 692-701, 2015Tradução . . Disponível em: https://doi.org/10.1080/00397911.2014.978504. Acesso em: 23 abr. 2024.
APA
Franco, M. S. F., Casagrande, G. A., Raminelli, C., Moura, S., Rossatto, M., Quina, F. H., et al. (2015). Ultrasound-promoted environmentally friendly synthesis of 5-(3,3,3-trifluoro-2-oxopropylidene)pyrrolidin-2-ones. Synthetic Communications, 45( 6), 692-701. doi:10.1080/00397911.2014.978504
NLM
Franco MSF, Casagrande GA, Raminelli C, Moura S, Rossatto M, Quina FH, Pereira CMP de, Flores AFC, Pizzuti L. Ultrasound-promoted environmentally friendly synthesis of 5-(3,3,3-trifluoro-2-oxopropylidene)pyrrolidin-2-ones [Internet]. Synthetic Communications. 2015 ; 45( 6): 692-701.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1080/00397911.2014.978504
Vancouver
Franco MSF, Casagrande GA, Raminelli C, Moura S, Rossatto M, Quina FH, Pereira CMP de, Flores AFC, Pizzuti L. Ultrasound-promoted environmentally friendly synthesis of 5-(3,3,3-trifluoro-2-oxopropylidene)pyrrolidin-2-ones [Internet]. Synthetic Communications. 2015 ; 45( 6): 692-701.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1080/00397911.2014.978504
Artigo de periodico
New approach to the synthesis of the natural product aripuanin (2015)
Lazaro, Aline S; Ribeiro, Pedro H. Zana; Sairre, Mirela I; Donate, Paulo Marcos
Fonte: Synthetic Communications. Unidade: FFCLRP
Assuntos: PRODUTOS NATURAIS (SÍNTESE QUÍMICA), SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
LAZARO, Aline S et al. New approach to the synthesis of the natural product aripuanin. Synthetic Communications, v. 45, n. 11, p. 1374-1378, 2015Tradução . . Disponível em: https://doi.org/10.1080/00397911.2015.1021426. Acesso em: 23 abr. 2024.
APA
Lazaro, A. S., Ribeiro, P. H. Z., Sairre, M. I., & Donate, P. M. (2015). New approach to the synthesis of the natural product aripuanin. Synthetic Communications, 45( 11), 1374-1378. doi:10.1080/00397911.2015.1021426
NLM
Lazaro AS, Ribeiro PHZ, Sairre MI, Donate PM. New approach to the synthesis of the natural product aripuanin [Internet]. Synthetic Communications. 2015 ; 45( 11): 1374-1378.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1080/00397911.2015.1021426
Vancouver
Lazaro AS, Ribeiro PHZ, Sairre MI, Donate PM. New approach to the synthesis of the natural product aripuanin [Internet]. Synthetic Communications. 2015 ; 45( 11): 1374-1378.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1080/00397911.2015.1021426
Artigo de periodico
Synthesis of some functionalized peptomers via UGI four-component reaction (2015)
Silva, Eduardo H. B; Emery, Flavio da Silva; Del Ponte, Gino; Donate, Paulo Marcos
Fonte: Synthetic Communications. Unidades: FCFRP, FFCLRP
Assuntos: PEPTÍDEOS, SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
SILVA, Eduardo H. B et al. Synthesis of some functionalized peptomers via UGI four-component reaction. Synthetic Communications, v. 45, n. 15, p. 1761-1767, 2015Tradução . . Disponível em: https://doi.org/10.1080/00397911.2015.1042591. Acesso em: 23 abr. 2024.
APA
Silva, E. H. B., Emery, F. da S., Del Ponte, G., & Donate, P. M. (2015). Synthesis of some functionalized peptomers via UGI four-component reaction. Synthetic Communications, 45( 15), 1761-1767. doi:10.1080/00397911.2015.1042591
NLM
Silva EHB, Emery F da S, Del Ponte G, Donate PM. Synthesis of some functionalized peptomers via UGI four-component reaction [Internet]. Synthetic Communications. 2015 ; 45( 15): 1761-1767.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1080/00397911.2015.1042591
Vancouver
Silva EHB, Emery F da S, Del Ponte G, Donate PM. Synthesis of some functionalized peptomers via UGI four-component reaction [Internet]. Synthetic Communications. 2015 ; 45( 15): 1761-1767.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1080/00397911.2015.1042591
Artigo de periodico
Stereoselective synthesis of novel Diels-Alder adducts of 'rô'-substituted cyclopentadiene (2012)
Camilo, Fernanda Ferraz; Gruber, Jonas
Fonte: Synthetic Communications. Unidade: IQ
Assuntos: REAÇÕES ORGÂNICAS, QUÍMICA ORGÂNICA
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ABNT
CAMILO, Fernanda Ferraz e GRUBER, Jonas. Stereoselective synthesis of novel Diels-Alder adducts of 'rô'-substituted cyclopentadiene. Synthetic Communications, v. 42, n. 3, p. 394-401, 2012Tradução . . Disponível em: https://doi.org/10.1080/00397911.2010.524962. Acesso em: 23 abr. 2024.
APA
Camilo, F. F., & Gruber, J. (2012). Stereoselective synthesis of novel Diels-Alder adducts of 'rô'-substituted cyclopentadiene. Synthetic Communications, 42( 3), 394-401. doi:10.1080/00397911.2010.524962
NLM
Camilo FF, Gruber J. Stereoselective synthesis of novel Diels-Alder adducts of 'rô'-substituted cyclopentadiene [Internet]. Synthetic Communications. 2012 ; 42( 3): 394-401.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1080/00397911.2010.524962
Vancouver
Camilo FF, Gruber J. Stereoselective synthesis of novel Diels-Alder adducts of 'rô'-substituted cyclopentadiene [Internet]. Synthetic Communications. 2012 ; 42( 3): 394-401.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1080/00397911.2010.524962
Artigo de periodico
Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis (2010)
Donnici, Claudio Luis; Pereira, Elaine Henriques Teixeira; Lopes, Júlio Cesar Dias; Marzorati, Liliana ; Wladislaw, Blanka
Fonte: Synthetic Communications. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
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ABNT
DONNICI, Claudio Luis et al. Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis. Synthetic Communications, v. 40, n. 3, p. 342-350, 2010Tradução . . Acesso em: 23 abr. 2024.
APA
Donnici, C. L., Pereira, E. H. T., Lopes, J. C. D., Marzorati, L., & Wladislaw, B. (2010). Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis. Synthetic Communications, 40( 3), 342-350.
NLM
Donnici CL, Pereira EHT, Lopes JCD, Marzorati L, Wladislaw B. Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis. Synthetic Communications. 2010 ; 40( 3): 342-350.[citado 2024 abr. 23 ]
Vancouver
Donnici CL, Pereira EHT, Lopes JCD, Marzorati L, Wladislaw B. Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis. Synthetic Communications. 2010 ; 40( 3): 342-350.[citado 2024 abr. 23 ]
Artigo de periodico
Hydroalumination of thioacetylenes: a versatile generation and reactions of 'alfa'-aluminate sulfides intermediates (2008)
Guerrero Júnior, P. G.; Dabdoub, Miguel Joaquim; Marques, F. A.; Wosch, C. L.; Baroni, A. C. M.; Ferreira, A. G.
Fonte: Synthetic Communications. Unidade: FFCLRP
Assunto: REAÇÕES QUÍMICAS
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ABNT
GUERRERO JÚNIOR, P. G. et al. Hydroalumination of thioacetylenes: a versatile generation and reactions of 'alfa'-aluminate sulfides intermediates. Synthetic Communications, v. 38, p. 4379-4394, 2008Tradução . . Acesso em: 23 abr. 2024.
APA
Guerrero Júnior, P. G., Dabdoub, M. J., Marques, F. A., Wosch, C. L., Baroni, A. C. M., & Ferreira, A. G. (2008). Hydroalumination of thioacetylenes: a versatile generation and reactions of 'alfa'-aluminate sulfides intermediates. Synthetic Communications, 38, 4379-4394.
NLM
Guerrero Júnior PG, Dabdoub MJ, Marques FA, Wosch CL, Baroni ACM, Ferreira AG. Hydroalumination of thioacetylenes: a versatile generation and reactions of 'alfa'-aluminate sulfides intermediates. Synthetic Communications. 2008 ; 38 4379-4394.[citado 2024 abr. 23 ]
Vancouver
Guerrero Júnior PG, Dabdoub MJ, Marques FA, Wosch CL, Baroni ACM, Ferreira AG. Hydroalumination of thioacetylenes: a versatile generation and reactions of 'alfa'-aluminate sulfides intermediates. Synthetic Communications. 2008 ; 38 4379-4394.[citado 2024 abr. 23 ]
Artigo de periodico
In-situ generation of n-butanethiol and its reaction with electron-deficient olefins (2008)
Gariani, Rogério Aparecido; Dos Santos, Alcindo Aparecido; Comasseto, João Valdir
Fonte: Synthetic Communications. Unidade: IQ
Assuntos: LÍQUIDOS IÔNICOS, CATÁLISE, TELÚRIO
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ABNT
GARIANI, Rogério Aparecido e DOS SANTOS, Alcindo Aparecido e COMASSETO, João Valdir. In-situ generation of n-butanethiol and its reaction with electron-deficient olefins. Synthetic Communications, v. 38, n. 5, p. 789-795, 2008Tradução . . Acesso em: 23 abr. 2024.
APA
Gariani, R. A., Dos Santos, A. A., & Comasseto, J. V. (2008). In-situ generation of n-butanethiol and its reaction with electron-deficient olefins. Synthetic Communications, 38( 5), 789-795.
NLM
Gariani RA, Dos Santos AA, Comasseto JV. In-situ generation of n-butanethiol and its reaction with electron-deficient olefins. Synthetic Communications. 2008 ; 38( 5): 789-795.[citado 2024 abr. 23 ]
Vancouver
Gariani RA, Dos Santos AA, Comasseto JV. In-situ generation of n-butanethiol and its reaction with electron-deficient olefins. Synthetic Communications. 2008 ; 38( 5): 789-795.[citado 2024 abr. 23 ]
Artigo de periodico
Opening of epoxide rings catalyzed by niobium pentachloride (2007)
Constantino, Maurício Gomes; Lacerda Júnior, Valdemar; Invernize, Paulo Roberto; Silva Filho, Luiz Carlos da; Silva, Gil Valdo José da
Fonte: Synthetic Communications. Unidade: FFCLRP
Assunto: SÍNTESE ORGÂNICA
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ABNT
CONSTANTINO, Maurício Gomes et al. Opening of epoxide rings catalyzed by niobium pentachloride. Synthetic Communications, v. 37, p. 3529-3539, 2007Tradução . . Acesso em: 23 abr. 2024.
APA
Constantino, M. G., Lacerda Júnior, V., Invernize, P. R., Silva Filho, L. C. da, & Silva, G. V. J. da. (2007). Opening of epoxide rings catalyzed by niobium pentachloride. Synthetic Communications, 37, 3529-3539.
NLM
Constantino MG, Lacerda Júnior V, Invernize PR, Silva Filho LC da, Silva GVJ da. Opening of epoxide rings catalyzed by niobium pentachloride. Synthetic Communications. 2007 ; 37 3529-3539.[citado 2024 abr. 23 ]
Vancouver
Constantino MG, Lacerda Júnior V, Invernize PR, Silva Filho LC da, Silva GVJ da. Opening of epoxide rings catalyzed by niobium pentachloride. Synthetic Communications. 2007 ; 37 3529-3539.[citado 2024 abr. 23 ]
Artigo de periodico
Synthesis of mesoionic 4-(para-substituted phenyl-5-2,4-dichlorophenyl)-1,3-4-thiadiazolium-2-aminides by direct cyclization via acylation of thiosemicarbazides (2006)
Britto, Marcelo Moreira; Almeida, Tânia Mara Grigolli; Leitão, Andrei ; Donnici, Claudio Luis; Lopes, Míriam Tereza Paz; Montanari, Carlos Alberto
Fonte: Synthetic Communications. Unidade: IQSC
Assuntos: QUÍMICA MÉDICA, SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA, REAÇÕES QUÍMICAS
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ABNT
BRITTO, Marcelo Moreira et al. Synthesis of mesoionic 4-(para-substituted phenyl-5-2,4-dichlorophenyl)-1,3-4-thiadiazolium-2-aminides by direct cyclization via acylation of thiosemicarbazides. Synthetic Communications, v. 36, n. 22, p. 3359-3369, 2006Tradução . . Disponível em: http://www.journalsonline.tandf.co.uk/openurl.asp?genre=article&id=doi:10.1080/00397910600941398. Acesso em: 23 abr. 2024.
APA
Britto, M. M., Almeida, T. M. G., Leitão, A., Donnici, C. L., Lopes, M. T. P., & Montanari, C. A. (2006). Synthesis of mesoionic 4-(para-substituted phenyl-5-2,4-dichlorophenyl)-1,3-4-thiadiazolium-2-aminides by direct cyclization via acylation of thiosemicarbazides. Synthetic Communications, 36( 22), 3359-3369. Recuperado de http://www.journalsonline.tandf.co.uk/openurl.asp?genre=article&id=doi:10.1080/00397910600941398
NLM
Britto MM, Almeida TMG, Leitão A, Donnici CL, Lopes MTP, Montanari CA. Synthesis of mesoionic 4-(para-substituted phenyl-5-2,4-dichlorophenyl)-1,3-4-thiadiazolium-2-aminides by direct cyclization via acylation of thiosemicarbazides [Internet]. Synthetic Communications. 2006 ; 36( 22): 3359-3369.[citado 2024 abr. 23 ] Available from: http://www.journalsonline.tandf.co.uk/openurl.asp?genre=article&id=doi:10.1080/00397910600941398
Vancouver
Britto MM, Almeida TMG, Leitão A, Donnici CL, Lopes MTP, Montanari CA. Synthesis of mesoionic 4-(para-substituted phenyl-5-2,4-dichlorophenyl)-1,3-4-thiadiazolium-2-aminides by direct cyclization via acylation of thiosemicarbazides [Internet]. Synthetic Communications. 2006 ; 36( 22): 3359-3369.[citado 2024 abr. 23 ] Available from: http://www.journalsonline.tandf.co.uk/openurl.asp?genre=article&id=doi:10.1080/00397910600941398
Artigo de periodico
Microwave-assisted protection of phenols as tert-butyldimethylsilyl (TBDMS) ethers under solvent-free conditions (2005)
Bastos, Erick Leite ; Ciscato, Luiz Francisco Monteiro Leite; Baader, Wilhelm Josef
Fonte: Synthetic Communications. Unidade: IQ
Assuntos: QUÍMICA ORGÂNICA, REAÇÕES QUÍMICAS
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ABNT
BASTOS, Erick Leite e CISCATO, Luiz Francisco Monteiro Leite e BAADER, Wilhelm Josef. Microwave-assisted protection of phenols as tert-butyldimethylsilyl (TBDMS) ethers under solvent-free conditions. Synthetic Communications, v. 35, n. 11, p. 1501-1509, 2005Tradução . . Acesso em: 23 abr. 2024.
APA
Bastos, E. L., Ciscato, L. F. M. L., & Baader, W. J. (2005). Microwave-assisted protection of phenols as tert-butyldimethylsilyl (TBDMS) ethers under solvent-free conditions. Synthetic Communications, 35( 11), 1501-1509.
NLM
Bastos EL, Ciscato LFML, Baader WJ. Microwave-assisted protection of phenols as tert-butyldimethylsilyl (TBDMS) ethers under solvent-free conditions. Synthetic Communications. 2005 ; 35( 11): 1501-1509.[citado 2024 abr. 23 ]
Vancouver
Bastos EL, Ciscato LFML, Baader WJ. Microwave-assisted protection of phenols as tert-butyldimethylsilyl (TBDMS) ethers under solvent-free conditions. Synthetic Communications. 2005 ; 35( 11): 1501-1509.[citado 2024 abr. 23 ]
Artigo de periodico
Efficient sonochemical synthesis of 3- and 4-electron withdrawing ring substituted N-alkyl-1,8-naphthalimides from the related anhydrides (2004)
Triboni, Eduardo Rezende; Berci Filho, Pedro; Berlinck, Roberto Gomes de Souza ; Politi, Mário José
Fonte: Synthetic Communications. Unidades: IQSC, IQ
Assunto: QUÍMICA ORGÂNICA
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ABNT
TRIBONI, Eduardo Rezende et al. Efficient sonochemical synthesis of 3- and 4-electron withdrawing ring substituted N-alkyl-1,8-naphthalimides from the related anhydrides. Synthetic Communications, v. 34, n. 11, p. 1989-1999, 2004Tradução . . Acesso em: 23 abr. 2024.
APA
Triboni, E. R., Berci Filho, P., Berlinck, R. G. de S., & Politi, M. J. (2004). Efficient sonochemical synthesis of 3- and 4-electron withdrawing ring substituted N-alkyl-1,8-naphthalimides from the related anhydrides. Synthetic Communications, 34( 11), 1989-1999.
NLM
Triboni ER, Berci Filho P, Berlinck RG de S, Politi MJ. Efficient sonochemical synthesis of 3- and 4-electron withdrawing ring substituted N-alkyl-1,8-naphthalimides from the related anhydrides. Synthetic Communications. 2004 ; 34( 11): 1989-1999.[citado 2024 abr. 23 ]
Vancouver
Triboni ER, Berci Filho P, Berlinck RG de S, Politi MJ. Efficient sonochemical synthesis of 3- and 4-electron withdrawing ring substituted N-alkyl-1,8-naphthalimides from the related anhydrides. Synthetic Communications. 2004 ; 34( 11): 1989-1999.[citado 2024 abr. 23 ]
Artigo de periodico
Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone (2004)
Clososki, Giuliano Cesar; Costa, Carlos E.; Missio, Lauri João; Cass, Quezia Bezerra; Comasseto, João Valdir
Fonte: Synthetic Communications. Unidade: IQ
Assuntos: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
CLOSOSKI, Giuliano Cesar et al. Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone. Synthetic Communications, v. 34, n. 5, p. 817-828, 2004Tradução . . Acesso em: 23 abr. 2024.
APA
Clososki, G. C., Costa, C. E., Missio, L. J., Cass, Q. B., & Comasseto, J. V. (2004). Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone. Synthetic Communications, 34( 5), 817-828.
NLM
Clososki GC, Costa CE, Missio LJ, Cass QB, Comasseto JV. Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone. Synthetic Communications. 2004 ; 34( 5): 817-828.[citado 2024 abr. 23 ]
Vancouver
Clososki GC, Costa CE, Missio LJ, Cass QB, Comasseto JV. Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone. Synthetic Communications. 2004 ; 34( 5): 817-828.[citado 2024 abr. 23 ]
Artigo de periodico
A Short enantioselective synthesis of (R)-(+)-gamma-Jasmolactone (2004)
Clososki, Giuliano Cesar; Missio, Lauri João; Comasseto, João Valdir
Fonte: Synthetic Communications. Unidade: IQ
Assuntos: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
CLOSOSKI, Giuliano Cesar e MISSIO, Lauri João e COMASSETO, João Valdir. A Short enantioselective synthesis of (R)-(+)-gamma-Jasmolactone. Synthetic Communications, v. 34, n. 13, p. 2371-2377, 2004Tradução . . Acesso em: 23 abr. 2024.
APA
Clososki, G. C., Missio, L. J., & Comasseto, J. V. (2004). A Short enantioselective synthesis of (R)-(+)-gamma-Jasmolactone. Synthetic Communications, 34( 13), 2371-2377.
NLM
Clososki GC, Missio LJ, Comasseto JV. A Short enantioselective synthesis of (R)-(+)-gamma-Jasmolactone. Synthetic Communications. 2004 ; 34( 13): 2371-2377.[citado 2024 abr. 23 ]
Vancouver
Clososki GC, Missio LJ, Comasseto JV. A Short enantioselective synthesis of (R)-(+)-gamma-Jasmolactone. Synthetic Communications. 2004 ; 34( 13): 2371-2377.[citado 2024 abr. 23 ]
Artigo de periodico
PTC sulfanylation of arylacetates (2003)
Marzorati, Liliana ; Silva, Marco Antonio da; Wladislaw, Blanka; Di Vitta, Cláudio
Fonte: Synthetic Communications. Unidade: IQ
Assunto: REAÇÕES ORGÂNICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARZORATI, Liliana et al. PTC sulfanylation of arylacetates. Synthetic Communications, v. 33, n. 20, p. 3491-3495, 2003Tradução . . Acesso em: 23 abr. 2024.
APA
Marzorati, L., Silva, M. A. da, Wladislaw, B., & Di Vitta, C. (2003). PTC sulfanylation of arylacetates. Synthetic Communications, 33( 20), 3491-3495.
NLM
Marzorati L, Silva MA da, Wladislaw B, Di Vitta C. PTC sulfanylation of arylacetates. Synthetic Communications. 2003 ; 33( 20): 3491-3495.[citado 2024 abr. 23 ]
Vancouver
Marzorati L, Silva MA da, Wladislaw B, Di Vitta C. PTC sulfanylation of arylacetates. Synthetic Communications. 2003 ; 33( 20): 3491-3495.[citado 2024 abr. 23 ]
Artigo de periodico
Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides (2003)
Stefani, Hélio Alexandre ; Petragnani, Nicola; Ascenso, Maria Fernanda Campanudo; Zeni, Gilson
Fonte: Synthetic Communications. Unidades: FCF, IQ
Assuntos: SÍNTESE ORGÂNICA, QUÍMICA FARMACÊUTICA, FARMACOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides. Synthetic Communications, v. 33, n. 12, p. 2161-2166, 2003Tradução . . Acesso em: 23 abr. 2024.
APA
Stefani, H. A., Petragnani, N., Ascenso, M. F. C., & Zeni, G. (2003). Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides. Synthetic Communications, 33( 12), 2161-2166.
NLM
Stefani HA, Petragnani N, Ascenso MFC, Zeni G. Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides. Synthetic Communications. 2003 ; 33( 12): 2161-2166.[citado 2024 abr. 23 ]
Vancouver
Stefani HA, Petragnani N, Ascenso MFC, Zeni G. Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides. Synthetic Communications. 2003 ; 33( 12): 2161-2166.[citado 2024 abr. 23 ]
Artigo de periodico
Conjugate addition of thiols and malonates to thiocinnamates under PTC conditions (2002)
Marzorati, Liliana ; Mattos, Marcos Carlos de; Wladislaw, Blanka; Di Vitta, Cláudio
Fonte: Synthetic Communications. Unidade: IQ
Assuntos: CATÁLISE, QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARZORATI, Liliana et al. Conjugate addition of thiols and malonates to thiocinnamates under PTC conditions. Synthetic Communications, v. 32, n. 9, p. 1427-1435, 2002Tradução . . Acesso em: 23 abr. 2024.
APA
Marzorati, L., Mattos, M. C. de, Wladislaw, B., & Di Vitta, C. (2002). Conjugate addition of thiols and malonates to thiocinnamates under PTC conditions. Synthetic Communications, 32( 9), 1427-1435.
NLM
Marzorati L, Mattos MC de, Wladislaw B, Di Vitta C. Conjugate addition of thiols and malonates to thiocinnamates under PTC conditions. Synthetic Communications. 2002 ; 32( 9): 1427-1435.[citado 2024 abr. 23 ]
Vancouver
Marzorati L, Mattos MC de, Wladislaw B, Di Vitta C. Conjugate addition of thiols and malonates to thiocinnamates under PTC conditions. Synthetic Communications. 2002 ; 32( 9): 1427-1435.[citado 2024 abr. 23 ]
Artigo de periodico
Synthesis of 4,5-dihydropyrroles by cyclofunctionalization from 'beta'-enamino esters (2002)
Stefani, Hélio Alexandre ; Avila, Elisabete de
Fonte: Synthetic Communications. Unidade: FCF
Assuntos: FARMACOLOGIA, COMPOSTOS HETEROCÍCLICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre e AVILA, Elisabete de. Synthesis of 4,5-dihydropyrroles by cyclofunctionalization from 'beta'-enamino esters. Synthetic Communications, v. 32, n. 13, p. 2041-2047, 2002Tradução . . Acesso em: 23 abr. 2024.
APA
Stefani, H. A., & Avila, E. de. (2002). Synthesis of 4,5-dihydropyrroles by cyclofunctionalization from 'beta'-enamino esters. Synthetic Communications, 32( 13), 2041-2047.
NLM
Stefani HA, Avila E de. Synthesis of 4,5-dihydropyrroles by cyclofunctionalization from 'beta'-enamino esters. Synthetic Communications. 2002 ; 32( 13): 2041-2047.[citado 2024 abr. 23 ]
Vancouver
Stefani HA, Avila E de. Synthesis of 4,5-dihydropyrroles by cyclofunctionalization from 'beta'-enamino esters. Synthetic Communications. 2002 ; 32( 13): 2041-2047.[citado 2024 abr. 23 ]
Artigo de periodico
Phase transfer catalysis in solid-liquid system as a selective method of mono-alkylation of alpha-sulfonyl thioesters (2002)
Wladislaw, Blanka; Marzorati, Liliana ; Neves, Reginas M. A.; Di Vitta, Cláudio
Fonte: Synthetic Communications. Unidade: IQ
Assuntos: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, FÍSICO-QUÍMICA, CATÁLISE, ALQUILAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WLADISLAW, Blanka et al. Phase transfer catalysis in solid-liquid system as a selective method of mono-alkylation of alpha-sulfonyl thioesters. Synthetic Communications, v. 32, n. 10, p. 1483-1487, 2002Tradução . . Acesso em: 23 abr. 2024.
APA
Wladislaw, B., Marzorati, L., Neves, R. M. A., & Di Vitta, C. (2002). Phase transfer catalysis in solid-liquid system as a selective method of mono-alkylation of alpha-sulfonyl thioesters. Synthetic Communications, 32( 10), 1483-1487.
NLM
Wladislaw B, Marzorati L, Neves RMA, Di Vitta C. Phase transfer catalysis in solid-liquid system as a selective method of mono-alkylation of alpha-sulfonyl thioesters. Synthetic Communications. 2002 ; 32( 10): 1483-1487.[citado 2024 abr. 23 ]
Vancouver
Wladislaw B, Marzorati L, Neves RMA, Di Vitta C. Phase transfer catalysis in solid-liquid system as a selective method of mono-alkylation of alpha-sulfonyl thioesters. Synthetic Communications. 2002 ; 32( 10): 1483-1487.[citado 2024 abr. 23 ]

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