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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
Source: Synthetic Communications. Unidade: FFCLRP
Subjects: 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: 05 dez. 2025.
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 2025 dez. 05 ] 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 2025 dez. 05 ] 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
Source: Synthetic Communications. Unidades: FCFRP, FFCLRP
Subjects: 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: 05 dez. 2025.
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 2025 dez. 05 ] 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 2025 dez. 05 ] 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
Source: Synthetic Communications. Unidade: IQ
Subjects: 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: 05 dez. 2025.
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 2025 dez. 05 ] 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 2025 dez. 05 ] 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
Source: 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: 05 dez. 2025.
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 2025 dez. 05 ]
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 2025 dez. 05 ]
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
Source: Synthetic Communications. Unidade: IQSC
Subjects: 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: 05 dez. 2025.
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 2025 dez. 05 ] 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 2025 dez. 05 ] 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
Source: Synthetic Communications. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, REAÇÕES QUÍMICAS
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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: 05 dez. 2025.
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 2025 dez. 05 ]
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 2025 dez. 05 ]
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
Source: 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: 05 dez. 2025.
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 2025 dez. 05 ]
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 2025 dez. 05 ]
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
Source: Synthetic Communications. Unidade: IQ
Subjects: 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: 05 dez. 2025.
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 2025 dez. 05 ]
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 2025 dez. 05 ]
Artigo de periodico
A Short enantioselective synthesis of (R)-(+)-gamma-Jasmolactone (2004)
Clososki, Giuliano Cesar; Missio, Lauri João; Comasseto, João Valdir
Source: Synthetic Communications. Unidade: IQ
Subjects: 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: 05 dez. 2025.
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 2025 dez. 05 ]
Vancouver
Clososki GC, Missio LJ, Comasseto JV. A Short enantioselective synthesis of (R)-(+)-gamma-Jasmolactone. Synthetic Communications. 2004 ; 34( 13): 2371-2377.[citado 2025 dez. 05 ]
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
Source: Synthetic Communications. Unidade: IQ
Subjects: CATÁLISE, QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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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: 05 dez. 2025.
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 2025 dez. 05 ]
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 2025 dez. 05 ]
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
Source: Synthetic Communications. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, FÍSICO-QUÍMICA, CATÁLISE, ALQUILAÇÃO
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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: 05 dez. 2025.
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 2025 dez. 05 ]
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 2025 dez. 05 ]
Artigo de periodico
Synthetic studies on the diels-alder adduct from 3,4-dimethoxyfuran and benzoquinone (2001)
Constantino, Maurício Gomes; Beatriz, Adilson; Silva, Gil Valdo José da; Zukerman-Schpector, Júlio
Source: Synthetic Communications. Unidades: FFCLRP, IQ
Assunto: QUÍMICA ORGÂNICA
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ABNT
CONSTANTINO, Maurício Gomes et al. Synthetic studies on the diels-alder adduct from 3,4-dimethoxyfuran and benzoquinone. Synthetic Communications, v. 31, n. 21, p. 3329-3336, 2001Tradução . . Disponível em: http://www.dekker.com/catalog/results.jsp?action=getSearchForm. Acesso em: 05 dez. 2025.
APA
Constantino, M. G., Beatriz, A., Silva, G. V. J. da, & Zukerman-Schpector, J. (2001). Synthetic studies on the diels-alder adduct from 3,4-dimethoxyfuran and benzoquinone. Synthetic Communications, 31( 21), 3329-3336. Recuperado de http://www.dekker.com/catalog/results.jsp?action=getSearchForm
NLM
Constantino MG, Beatriz A, Silva GVJ da, Zukerman-Schpector J. Synthetic studies on the diels-alder adduct from 3,4-dimethoxyfuran and benzoquinone [Internet]. Synthetic Communications. 2001 ; 31( 21): 3329-3336.[citado 2025 dez. 05 ] Available from: http://www.dekker.com/catalog/results.jsp?action=getSearchForm
Vancouver
Constantino MG, Beatriz A, Silva GVJ da, Zukerman-Schpector J. Synthetic studies on the diels-alder adduct from 3,4-dimethoxyfuran and benzoquinone [Internet]. Synthetic Communications. 2001 ; 31( 21): 3329-3336.[citado 2025 dez. 05 ] Available from: http://www.dekker.com/catalog/results.jsp?action=getSearchForm
Artigo de periodico
Reaction of 3-alkenols with thallium trinitrate: an unexpected and useful ring contraction (2000)
Ferraz, Helena Maria Carvalho; Santos, Andréa P; Silva Junior, Luiz Fernando da; Vieira, Thiago de O
Source: Synthetic Communications. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
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ABNT
FERRAZ, Helena Maria Carvalho et al. Reaction of 3-alkenols with thallium trinitrate: an unexpected and useful ring contraction. Synthetic Communications, v. 30, n. 4, p. 751-762, 2000Tradução . . Acesso em: 05 dez. 2025.
APA
Ferraz, H. M. C., Santos, A. P., Silva Junior, L. F. da, & Vieira, T. de O. (2000). Reaction of 3-alkenols with thallium trinitrate: an unexpected and useful ring contraction. Synthetic Communications, 30( 4), 751-762.
NLM
Ferraz HMC, Santos AP, Silva Junior LF da, Vieira T de O. Reaction of 3-alkenols with thallium trinitrate: an unexpected and useful ring contraction. Synthetic Communications. 2000 ; 30( 4): 751-762.[citado 2025 dez. 05 ]
Vancouver
Ferraz HMC, Santos AP, Silva Junior LF da, Vieira T de O. Reaction of 3-alkenols with thallium trinitrate: an unexpected and useful ring contraction. Synthetic Communications. 2000 ; 30( 4): 751-762.[citado 2025 dez. 05 ]
Artigo de periodico
Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution (2000)
Di Vitta, Cláudio ; Wladislaw, Blanka; Marzorati, Liliana
Source: Synthetic Communications. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, ENXOFRE
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ABNT
DI VITTA, Cláudio e WLADISLAW, Blanka e MARZORATI, Liliana. Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution. Synthetic Communications, v. 30, n. 18, p. 3413-3422, 2000Tradução . . Acesso em: 05 dez. 2025.
APA
Di Vitta, C., Wladislaw, B., & Marzorati, L. (2000). Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution. Synthetic Communications, 30( 18), 3413-3422.
NLM
Di Vitta C, Wladislaw B, Marzorati L. Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution. Synthetic Communications. 2000 ; 30( 18): 3413-3422.[citado 2025 dez. 05 ]
Vancouver
Di Vitta C, Wladislaw B, Marzorati L. Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution. Synthetic Communications. 2000 ; 30( 18): 3413-3422.[citado 2025 dez. 05 ]
Artigo de periodico
Synthesis of substituted 'GAMA'- butyrolactones: 'BETA'-hydroxymethyl-, 'BETA'-methylene and cyclopropane derivatives (1999)
Donate, Paulo Marcos; Constantino, Maurício Gomes; Silva, Rosangela da; Pedersoli, Susimaire
Source: Synthetic Communications. Unidade: FFCLRP
Assunto: QUÍMICA ORGÂNICA
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ABNT
DONATE, Paulo Marcos et al. Synthesis of substituted 'GAMA'- butyrolactones: 'BETA'-hydroxymethyl-, 'BETA'-methylene and cyclopropane derivatives. Synthetic Communications, v. 29, n. 17, p. 2923-2936, 1999Tradução . . Acesso em: 05 dez. 2025.
APA
Donate, P. M., Constantino, M. G., Silva, R. da, & Pedersoli, S. (1999). Synthesis of substituted 'GAMA'- butyrolactones: 'BETA'-hydroxymethyl-, 'BETA'-methylene and cyclopropane derivatives. Synthetic Communications, 29( 17), 2923-2936.
NLM
Donate PM, Constantino MG, Silva R da, Pedersoli S. Synthesis of substituted 'GAMA'- butyrolactones: 'BETA'-hydroxymethyl-, 'BETA'-methylene and cyclopropane derivatives. Synthetic Communications. 1999 ; 29( 17): 2923-2936.[citado 2025 dez. 05 ]
Vancouver
Donate PM, Constantino MG, Silva R da, Pedersoli S. Synthesis of substituted 'GAMA'- butyrolactones: 'BETA'-hydroxymethyl-, 'BETA'-methylene and cyclopropane derivatives. Synthetic Communications. 1999 ; 29( 17): 2923-2936.[citado 2025 dez. 05 ]
Artigo de periodico
Reaction of ´beta´,´gama´-unsaturated carboxylic acids with thallium triacetate (TTA): lactonization vs oxidative decarboxylation (1999)
Ferraz, Helena Maria Carvalho; Grazini, Mônica V A; Silva Junior, Luiz Fernando da; Longo Junior, Luiz S
Source: Synthetic Communications. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ, Helena Maria Carvalho et al. Reaction of ´beta´,´gama´-unsaturated carboxylic acids with thallium triacetate (TTA): lactonization vs oxidative decarboxylation. Synthetic Communications, v. 29, n. 11, p. 1953-1964, 1999Tradução . . Acesso em: 05 dez. 2025.
APA
Ferraz, H. M. C., Grazini, M. V. A., Silva Junior, L. F. da, & Longo Junior, L. S. (1999). Reaction of ´beta´,´gama´-unsaturated carboxylic acids with thallium triacetate (TTA): lactonization vs oxidative decarboxylation. Synthetic Communications, 29( 11), 1953-1964.
NLM
Ferraz HMC, Grazini MVA, Silva Junior LF da, Longo Junior LS. Reaction of ´beta´,´gama´-unsaturated carboxylic acids with thallium triacetate (TTA): lactonization vs oxidative decarboxylation. Synthetic Communications. 1999 ; 29( 11): 1953-1964.[citado 2025 dez. 05 ]
Vancouver
Ferraz HMC, Grazini MVA, Silva Junior LF da, Longo Junior LS. Reaction of ´beta´,´gama´-unsaturated carboxylic acids with thallium triacetate (TTA): lactonization vs oxidative decarboxylation. Synthetic Communications. 1999 ; 29( 11): 1953-1964.[citado 2025 dez. 05 ]
Artigo de periodico
A novel and easy de-ethoxycarbonylation of `alfa´-substituted malonic esters (1998)
Melo, Júlio O F; Pereira, Elaine H Teixeira; Donnici, Claudio Luis; Wladislaw, Blanka; Marzorati, Liliana
Source: Synthetic Communications. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, Júlio O F et al. A novel and easy de-ethoxycarbonylation of `alfa´-substituted malonic esters. Synthetic Communications, v. 28, n. 22, p. 4179-4185, 1998Tradução . . Acesso em: 05 dez. 2025.
APA
Melo, J. O. F., Pereira, E. H. T., Donnici, C. L., Wladislaw, B., & Marzorati, L. (1998). A novel and easy de-ethoxycarbonylation of `alfa´-substituted malonic esters. Synthetic Communications, 28( 22), 4179-4185.
NLM
Melo JOF, Pereira EHT, Donnici CL, Wladislaw B, Marzorati L. A novel and easy de-ethoxycarbonylation of `alfa´-substituted malonic esters. Synthetic Communications. 1998 ; 28( 22): 4179-4185.[citado 2025 dez. 05 ]
Vancouver
Melo JOF, Pereira EHT, Donnici CL, Wladislaw B, Marzorati L. A novel and easy de-ethoxycarbonylation of `alfa´-substituted malonic esters. Synthetic Communications. 1998 ; 28( 22): 4179-4185.[citado 2025 dez. 05 ]
Artigo de periodico
Highly functionalized selenocyclopropanes from 1-halo-1-chalcogeno alkenes (1998)
Stefani, Hélio Alexandre ; Petragnani, Nicola; Comasseto, João Valdir; Braga, Antônio L; Menezes, Paulo H
Source: Synthetic Communications. Unidades: FCF, IQ
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Highly functionalized selenocyclopropanes from 1-halo-1-chalcogeno alkenes. Synthetic Communications, v. 28, n. 9, p. 1667-1677, 1998Tradução . . Acesso em: 05 dez. 2025.
APA
Stefani, H. A., Petragnani, N., Comasseto, J. V., Braga, A. L., & Menezes, P. H. (1998). Highly functionalized selenocyclopropanes from 1-halo-1-chalcogeno alkenes. Synthetic Communications, 28( 9), 1667-1677.
NLM
Stefani HA, Petragnani N, Comasseto JV, Braga AL, Menezes PH. Highly functionalized selenocyclopropanes from 1-halo-1-chalcogeno alkenes. Synthetic Communications. 1998 ; 28( 9): 1667-1677.[citado 2025 dez. 05 ]
Vancouver
Stefani HA, Petragnani N, Comasseto JV, Braga AL, Menezes PH. Highly functionalized selenocyclopropanes from 1-halo-1-chalcogeno alkenes. Synthetic Communications. 1998 ; 28( 9): 1667-1677.[citado 2025 dez. 05 ]
Artigo de periodico
Cyclization of olefinic benzyl ethers with aryltellurium trichlorides (1992)
Comasseto, João Valdir; Grazini, M V A
Source: Synthetic Communications. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, REAÇÕES QUÍMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COMASSETO, João Valdir e GRAZINI, M V A. Cyclization of olefinic benzyl ethers with aryltellurium trichlorides. Synthetic Communications, v. 22, n. 6 , p. 949-54, 1992Tradução . . Acesso em: 05 dez. 2025.
APA
Comasseto, J. V., & Grazini, M. V. A. (1992). Cyclization of olefinic benzyl ethers with aryltellurium trichlorides. Synthetic Communications, 22( 6 ), 949-54.
NLM
Comasseto JV, Grazini MVA. Cyclization of olefinic benzyl ethers with aryltellurium trichlorides. Synthetic Communications. 1992 ;22( 6 ): 949-54.[citado 2025 dez. 05 ]
Vancouver
Comasseto JV, Grazini MVA. Cyclization of olefinic benzyl ethers with aryltellurium trichlorides. Synthetic Communications. 1992 ;22( 6 ): 949-54.[citado 2025 dez. 05 ]
Artigo de periodico
Thallium (iii) salts -induced lactonizations of unsaturated carboxilic acids (1992)
Ferraz, Helena Maria Carvalho; Ribeiro, C M R
Source: Synthetic Communications. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, REAGENTES ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ, Helena Maria Carvalho e RIBEIRO, C M R. Thallium (iii) salts -induced lactonizations of unsaturated carboxilic acids. Synthetic Communications, v. 22, n. 3 , p. 399-404, 1992Tradução . . Acesso em: 05 dez. 2025.
APA
Ferraz, H. M. C., & Ribeiro, C. M. R. (1992). Thallium (iii) salts -induced lactonizations of unsaturated carboxilic acids. Synthetic Communications, 22( 3 ), 399-404.
NLM
Ferraz HMC, Ribeiro CMR. Thallium (iii) salts -induced lactonizations of unsaturated carboxilic acids. Synthetic Communications. 1992 ;22( 3 ): 399-404.[citado 2025 dez. 05 ]
Vancouver
Ferraz HMC, Ribeiro CMR. Thallium (iii) salts -induced lactonizations of unsaturated carboxilic acids. Synthetic Communications. 1992 ;22( 3 ): 399-404.[citado 2025 dez. 05 ]

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