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Artigo de periodico
Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes (2009)
Ferraz, Helena Maria Carvalho; Carneiro, Vânia Maria Teixeira; Silva Junior, Luiz Fernando da
Source: Synthesis. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, TÁLIO, NITRATOS, CARBONO
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ABNT
FERRAZ, Helena Maria Carvalho e CARNEIRO, Vânia Maria Teixeira e SILVA JUNIOR, Luiz Fernando da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes. Synthesis, n. 3, p. 385-388, 2009Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf. Acesso em: 13 nov. 2024.
APA
Ferraz, H. M. C., Carneiro, V. M. T., & Silva Junior, L. F. da. (2009). Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes. Synthesis, ( 3), 385-388. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
NLM
Ferraz HMC, Carneiro VMT, Silva Junior LF da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes [Internet]. Synthesis. 2009 ;( 3): 385-388.[citado 2024 nov. 13 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
Vancouver
Ferraz HMC, Carneiro VMT, Silva Junior LF da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes [Internet]. Synthesis. 2009 ;( 3): 385-388.[citado 2024 nov. 13 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
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: 13 nov. 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 nov. 13 ] 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 nov. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
Artigo de periodico
An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization (2009)
Silva Jr., Luiz Fernando da; Quintiliano, Samir Augusto Pino
Source: Tetrahedron Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
SILVA JR., Luiz Fernando da e QUINTILIANO, Samir Augusto Pino. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters, v. 50, n. 19, p. 2256-2260, 2009Tradução . . Acesso em: 13 nov. 2024.
APA
Silva Jr., L. F. da, & Quintiliano, S. A. P. (2009). An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters, 50( 19), 2256-2260.
NLM
Silva Jr. LF da, Quintiliano SAP. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters. 2009 ; 50( 19): 2256-2260.[citado 2024 nov. 13 ]
Vancouver
Silva Jr. LF da, Quintiliano SAP. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters. 2009 ; 50( 19): 2256-2260.[citado 2024 nov. 13 ]
Artigo de periodico
Uncovering false positives on a virtual screening search for cruzain inhibitors (2008)
Malvezzi, Alberto; Rezende, Leandro de; Izidoro, Mario Augusto; Cezari, Maria Helena Sedenho; Juliano, Luiz; Amaral, Antonia Tavares do
Source: Bioorganic & Medicinal Chemistry Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, PEROXIDASE
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ABNT
MALVEZZI, Alberto et al. Uncovering false positives on a virtual screening search for cruzain inhibitors. Bioorganic & Medicinal Chemistry Letters, v. 18, n. 1, p. 350-354, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2007.10.068. Acesso em: 13 nov. 2024.
APA
Malvezzi, A., Rezende, L. de, Izidoro, M. A., Cezari, M. H. S., Juliano, L., & Amaral, A. T. do. (2008). Uncovering false positives on a virtual screening search for cruzain inhibitors. Bioorganic & Medicinal Chemistry Letters, 18( 1), 350-354. doi:10.1016/j.bmcl.2007.10.068
NLM
Malvezzi A, Rezende L de, Izidoro MA, Cezari MHS, Juliano L, Amaral AT do. Uncovering false positives on a virtual screening search for cruzain inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2008 ; 18( 1): 350-354.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.bmcl.2007.10.068
Vancouver
Malvezzi A, Rezende L de, Izidoro MA, Cezari MHS, Juliano L, Amaral AT do. Uncovering false positives on a virtual screening search for cruzain inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2008 ; 18( 1): 350-354.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.bmcl.2007.10.068
Artigo de periodico
Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides (2008)
Comasseto, João Valdir; Gariani, Rogério Aparecido; Princival, Jefferson Luiz; Dos Santos, Alcindo Aparecido; Zinn, Fabiano Kauer
Source: Journal of Organometallic Chemistry. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
COMASSETO, João Valdir et al. Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides. Journal of Organometallic Chemistry, v. 693, n. 17, p. 2929-2936, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2008.06.014. Acesso em: 13 nov. 2024.
APA
Comasseto, J. V., Gariani, R. A., Princival, J. L., Dos Santos, A. A., & Zinn, F. K. (2008). Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides. Journal of Organometallic Chemistry, 693( 17), 2929-2936. doi:10.1016/j.jorganchem.2008.06.014
NLM
Comasseto JV, Gariani RA, Princival JL, Dos Santos AA, Zinn FK. Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides [Internet]. Journal of Organometallic Chemistry. 2008 ; 693( 17): 2929-2936.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.06.014
Vancouver
Comasseto JV, Gariani RA, Princival JL, Dos Santos AA, Zinn FK. Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides [Internet]. Journal of Organometallic Chemistry. 2008 ; 693( 17): 2929-2936.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.06.014
Artigo de periodico
Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435) (2007)
Raminelli, Cristiano; Kagohara, Edna; Pellizari, Vivian Helena; Comasseto, João Valdir; Andrade, Leandro Helgueira ; Porto, Andre Luiz Meleiro
Source: Enzyme and Microbial Technology. Unidades: ICB, IQ, IQSC
Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA
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ABNT
RAMINELLI, Cristiano et al. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435). Enzyme and Microbial Technology, v. 40, n. 2, p. 362-369, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.enzmictec.2006.06.002. Acesso em: 13 nov. 2024.
APA
Raminelli, C., Kagohara, E., Pellizari, V. H., Comasseto, J. V., Andrade, L. H., & Porto, A. L. M. (2007). Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435). Enzyme and Microbial Technology, 40( 2), 362-369. doi:10.1016/j.enzmictec.2006.06.002
NLM
Raminelli C, Kagohara E, Pellizari VH, Comasseto JV, Andrade LH, Porto ALM. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435) [Internet]. Enzyme and Microbial Technology. 2007 ; 40( 2): 362-369.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
Vancouver
Raminelli C, Kagohara E, Pellizari VH, Comasseto JV, Andrade LH, Porto ALM. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435) [Internet]. Enzyme and Microbial Technology. 2007 ; 40( 2): 362-369.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
Artigo de periodico
Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide (2007)
Valadares, Marize Campos; Rezende, Kênnia Rocha; Pereira, Enir Raquel Tavares; Sousa, Mariana Côrtes de; Gonçalves Santiago, Bruno; Assis, Juliana Cipriano de; Kato, Massuo Jorge
Source: Food and Chemical Toxicology. Unidade: IQ
Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA
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ABNT
VALADARES, Marize Campos et al. Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide. Food and Chemical Toxicology, v. 45, n. 10, p. 1975-1978, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2007.04.016. Acesso em: 13 nov. 2024.
APA
Valadares, M. C., Rezende, K. R., Pereira, E. R. T., Sousa, M. C. de, Gonçalves Santiago, B., Assis, J. C. de, & Kato, M. J. (2007). Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide. Food and Chemical Toxicology, 45( 10), 1975-1978. doi:10.1016/j.fct.2007.04.016
NLM
Valadares MC, Rezende KR, Pereira ERT, Sousa MC de, Gonçalves Santiago B, Assis JC de, Kato MJ. Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide [Internet]. Food and Chemical Toxicology. 2007 ; 45( 10): 1975-1978.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.fct.2007.04.016
Vancouver
Valadares MC, Rezende KR, Pereira ERT, Sousa MC de, Gonçalves Santiago B, Assis JC de, Kato MJ. Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide [Internet]. Food and Chemical Toxicology. 2007 ; 45( 10): 1975-1978.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.fct.2007.04.016
Artigo de periodico
The diorgano dichalcogenides addition to benzyne under mild conditions (2007)
Toledo, Fabiano Travanca; Marques, Henrique; Comasseto, João Valdir; Raminelli, Cristiano
Source: Tetrahedron Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
TOLEDO, Fabiano Travanca et al. The diorgano dichalcogenides addition to benzyne under mild conditions. Tetrahedron Letters, v. 48, n. 46, p. 8125-8127, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.09.111. Acesso em: 13 nov. 2024.
APA
Toledo, F. T., Marques, H., Comasseto, J. V., & Raminelli, C. (2007). The diorgano dichalcogenides addition to benzyne under mild conditions. Tetrahedron Letters, 48( 46), 8125-8127. doi:10.1016/j.tetlet.2007.09.111
NLM
Toledo FT, Marques H, Comasseto JV, Raminelli C. The diorgano dichalcogenides addition to benzyne under mild conditions [Internet]. Tetrahedron Letters. 2007 ; 48( 46): 8125-8127.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2007.09.111
Vancouver
Toledo FT, Marques H, Comasseto JV, Raminelli C. The diorgano dichalcogenides addition to benzyne under mild conditions [Internet]. Tetrahedron Letters. 2007 ; 48( 46): 8125-8127.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2007.09.111
Artigo de periodico
Synthetic approaches to naturally occurring ten-membered-ring lactones (2007)
Ferraz, Helena Maria Carvalho; Bombonato, Fernanda Irene; Longo Junior, Luiz Sidney
Source: Synthesis. Unidade: IQ
Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA
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ABNT
FERRAZ, Helena Maria Carvalho e BOMBONATO, Fernanda Irene e LONGO JUNIOR, Luiz Sidney. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis, n. 21, p. 3261-3285, 2007Tradução . . Acesso em: 13 nov. 2024.
APA
Ferraz, H. M. C., Bombonato, F. I., & Longo Junior, L. S. (2007). Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis, ( 21), 3261-3285.
NLM
Ferraz HMC, Bombonato FI, Longo Junior LS. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis. 2007 ;( 21): 3261-3285.[citado 2024 nov. 13 ]
Vancouver
Ferraz HMC, Bombonato FI, Longo Junior LS. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis. 2007 ;( 21): 3261-3285.[citado 2024 nov. 13 ]
Artigo de periodico
New methodology for the preparation of N-tosyl aziridine-2-carboxylates (2007)
Marzorati, Liliana ; Barazzone, Giovana Cappio; Bueno Filho, Marco Antonio; Wladislaw, Blanka; Di Vitta, Cláudio
Source: Tetrahedron Letters. Unidade: IQ
Subjects: COMPOSTOS ORGÂNICOS, QUÍMICA ORGÂNICA
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ABNT
MARZORATI, Liliana et al. New methodology for the preparation of N-tosyl aziridine-2-carboxylates. Tetrahedron Letters, v. 48, n. 37, p. 6509-6513, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.07.054. Acesso em: 13 nov. 2024.
APA
Marzorati, L., Barazzone, G. C., Bueno Filho, M. A., Wladislaw, B., & Di Vitta, C. (2007). New methodology for the preparation of N-tosyl aziridine-2-carboxylates. Tetrahedron Letters, 48( 37), 6509-6513. doi:10.1016/j.tetlet.2007.07.054
NLM
Marzorati L, Barazzone GC, Bueno Filho MA, Wladislaw B, Di Vitta C. New methodology for the preparation of N-tosyl aziridine-2-carboxylates [Internet]. Tetrahedron Letters. 2007 ; 48( 37): 6509-6513.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2007.07.054
Vancouver
Marzorati L, Barazzone GC, Bueno Filho MA, Wladislaw B, Di Vitta C. New methodology for the preparation of N-tosyl aziridine-2-carboxylates [Internet]. Tetrahedron Letters. 2007 ; 48( 37): 6509-6513.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2007.07.054
Artigo de periodico
Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol (2006)
Cunha, Rodrigo Luiz Oliveira Rodrigues; Zukerman-Schpector, Júlio; Caracelli, Ignez; Comasseto, João Valdir
Source: Journal of Organometallic Chemistry. Unidade: IQ
Subjects: TELÚRIO, QUÍMICA ORGÂNICA
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ABNT
CUNHA, Rodrigo Luiz Oliveira Rodrigues et al. Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol. Journal of Organometallic Chemistry, v. 691, n. 23, p. 4807-4815, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2006.05.055. Acesso em: 13 nov. 2024.
APA
Cunha, R. L. O. R., Zukerman-Schpector, J., Caracelli, I., & Comasseto, J. V. (2006). Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol. Journal of Organometallic Chemistry, 691( 23), 4807-4815. doi:10.1016/j.jorganchem.2006.05.055
NLM
Cunha RLOR, Zukerman-Schpector J, Caracelli I, Comasseto JV. Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol [Internet]. Journal of Organometallic Chemistry. 2006 ; 691( 23): 4807-4815.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.jorganchem.2006.05.055
Vancouver
Cunha RLOR, Zukerman-Schpector J, Caracelli I, Comasseto JV. Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol [Internet]. Journal of Organometallic Chemistry. 2006 ; 691( 23): 4807-4815.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.jorganchem.2006.05.055
Artigo de periodico
Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin (2006)
Dos Santos, Alcindo Aparecido; Ferrarini, Renan dos Santos; Princival, Jefferson Luiz; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, TELÚRIO, LÍTIO
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ABNT
DOS SANTOS, Alcindo Aparecido et al. Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin. Tetrahedron Letters, v. 47, n. 50, p. 8933-8935, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.10.039. Acesso em: 13 nov. 2024.
APA
Dos Santos, A. A., Ferrarini, R. dos S., Princival, J. L., & Comasseto, J. V. (2006). Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin. Tetrahedron Letters, 47( 50), 8933-8935. doi:10.1016/j.tetlet.2006.10.039
NLM
Dos Santos AA, Ferrarini R dos S, Princival JL, Comasseto JV. Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin [Internet]. Tetrahedron Letters. 2006 ; 47( 50): 8933-8935.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039
Vancouver
Dos Santos AA, Ferrarini R dos S, Princival JL, Comasseto JV. Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin [Internet]. Tetrahedron Letters. 2006 ; 47( 50): 8933-8935.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039
Artigo de periodico
Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S (2006)
Zukerman-Schpector, Júlio; Silva, Rafael Oliveira da; Olivato, Paulo Roberto ; Vinhato, Elisângela; Rodrigues, Alessandro; Cerqueira Júnior, Carlos Rogério
Source: Zeitschrift für Kristallographie - New Crystal Structures. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
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ABNT
ZUKERMAN-SCHPECTOR, Júlio et al. Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S. Zeitschrift für Kristallographie - New Crystal Structures, v. 221, n. 3, p. 311-312, 2006Tradução . . Acesso em: 13 nov. 2024.
APA
Zukerman-Schpector, J., Silva, R. O. da, Olivato, P. R., Vinhato, E., Rodrigues, A., & Cerqueira Júnior, C. R. (2006). Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S. Zeitschrift für Kristallographie - New Crystal Structures, 221( 3), 311-312.
NLM
Zukerman-Schpector J, Silva RO da, Olivato PR, Vinhato E, Rodrigues A, Cerqueira Júnior CR. Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S. Zeitschrift für Kristallographie - New Crystal Structures. 2006 ; 221( 3): 311-312.[citado 2024 nov. 13 ]
Vancouver
Zukerman-Schpector J, Silva RO da, Olivato PR, Vinhato E, Rodrigues A, Cerqueira Júnior CR. Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S. Zeitschrift für Kristallographie - New Crystal Structures. 2006 ; 221( 3): 311-312.[citado 2024 nov. 13 ]
Artigo de periodico
Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides (2006)
Dos Santos, Alcindo Aparecido; Da Costa, Carlos E.; Princival, Jefferson Luiz; Comasseto, João Valdir
Source: Tetrahedron - Asymmetry. Unidade: IQ
Subjects: LIPASE, QUÍMICA ORGÂNICA
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ABNT
DOS SANTOS, Alcindo Aparecido et al. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides. Tetrahedron - Asymmetry, v. 17, n. 15, p. 2252-2259, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2006.07.024. Acesso em: 13 nov. 2024.
APA
Dos Santos, A. A., Da Costa, C. E., Princival, J. L., & Comasseto, J. V. (2006). Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides. Tetrahedron - Asymmetry, 17( 15), 2252-2259. doi:10.1016/j.tetasy.2006.07.024
NLM
Dos Santos AA, Da Costa CE, Princival JL, Comasseto JV. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 15): 2252-2259.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.024
Vancouver
Dos Santos AA, Da Costa CE, Princival JL, Comasseto JV. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 15): 2252-2259.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.024
Artigo de periodico
Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton (2006)
Ferraz, Helena Maria Carvalho; Vieira, Tiago O.; Silva Jr., Luiz Fernando da
Source: Synthesis. Unidade: IQ
Subjects: TÁLIO, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ, Helena Maria Carvalho e VIEIRA, Tiago O. e SILVA JR., Luiz Fernando da. Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis, n. 16, p. 2748-2752, 2006Tradução . . Acesso em: 13 nov. 2024.
APA
Ferraz, H. M. C., Vieira, T. O., & Silva Jr., L. F. da. (2006). Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis, ( 16), 2748-2752.
NLM
Ferraz HMC, Vieira TO, Silva Jr. LF da. Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis. 2006 ;( 16): 2748-2752.[citado 2024 nov. 13 ]
Vancouver
Ferraz HMC, Vieira TO, Silva Jr. LF da. Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis. 2006 ;( 16): 2748-2752.[citado 2024 nov. 13 ]
Artigo de periodico
Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane] (2006)
Bastos, Erick Leite ; Ciscato, Luiz Francisco Monteiro Leite; Weiss, Dieter; Beckert, Rainer; Baader, Wilhelm Josef
Source: Synthesis. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BASTOS, Erick Leite et al. Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane]. Synthesis, n. 15, p. , 2006Tradução . . Disponível em: https://doi.org/10.1055/s-2006-942357. Acesso em: 13 nov. 2024.
APA
Bastos, E. L., Ciscato, L. F. M. L., Weiss, D., Beckert, R., & Baader, W. J. (2006). Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane]. Synthesis, ( 15), . doi:10.1055/s-2006-942357
NLM
Bastos EL, Ciscato LFML, Weiss D, Beckert R, Baader WJ. Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane] [Internet]. Synthesis. 2006 ;( 15): .[citado 2024 nov. 13 ] Available from: https://doi.org/10.1055/s-2006-942357
Vancouver
Bastos EL, Ciscato LFML, Weiss D, Beckert R, Baader WJ. Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane] [Internet]. Synthesis. 2006 ;( 15): .[citado 2024 nov. 13 ] Available from: https://doi.org/10.1055/s-2006-942357
Artigo de periodico
Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435) (2006)
Vieira, Tiago de Oliveira; Ferraz, Helena Maria Carvalho; Andrade, Leandro Helgueira ; Porto, Andre Luiz Meleiro
Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC
Subjects: CANDIDA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIEIRA, Tiago de Oliveira et al. Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, v. 17, n. 13, p. 1990-1994, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2006.07.014. Acesso em: 13 nov. 2024.
APA
Vieira, T. de O., Ferraz, H. M. C., Andrade, L. H., & Porto, A. L. M. (2006). Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, 17( 13), 1990-1994. doi:10.1016/j.tetasy.2006.07.014
NLM
Vieira T de O, Ferraz HMC, Andrade LH, Porto ALM. Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 13): 1990-1994.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.014
Vancouver
Vieira T de O, Ferraz HMC, Andrade LH, Porto ALM. Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 13): 1990-1994.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.014
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 13 nov. 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 nov. 13 ] 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 nov. 13 ] Available from: https://doi.org/10.1016/j.tet.2006.06.051
Artigo de periodico
Crystal structure of cis-4-tert-butyl-2-(4-nitrophenylsulfonyl)cyclohexanone, 'C IND. 16''H IND. 21''NO IND. 5'S (2006)
Zukerman-Schpector, Júlio; Maganhi, Stella Hernandez; Olivato, Paulo Roberto ; Vinhato, Elisângela; Cerqueira Júnior, Carlos Rogério
Source: Zeitschrift für Kristallographie - New Crystal Structures. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZUKERMAN-SCHPECTOR, Júlio et al. Crystal structure of cis-4-tert-butyl-2-(4-nitrophenylsulfonyl)cyclohexanone, 'C IND. 16''H IND. 21''NO IND. 5'S. Zeitschrift für Kristallographie - New Crystal Structures, v. 221, n. 2, p. 165-166, 2006Tradução . . Acesso em: 13 nov. 2024.
APA
Zukerman-Schpector, J., Maganhi, S. H., Olivato, P. R., Vinhato, E., & Cerqueira Júnior, C. R. (2006). Crystal structure of cis-4-tert-butyl-2-(4-nitrophenylsulfonyl)cyclohexanone, 'C IND. 16''H IND. 21''NO IND. 5'S. Zeitschrift für Kristallographie - New Crystal Structures, 221( 2), 165-166.
NLM
Zukerman-Schpector J, Maganhi SH, Olivato PR, Vinhato E, Cerqueira Júnior CR. Crystal structure of cis-4-tert-butyl-2-(4-nitrophenylsulfonyl)cyclohexanone, 'C IND. 16''H IND. 21''NO IND. 5'S. Zeitschrift für Kristallographie - New Crystal Structures. 2006 ; 221( 2): 165-166.[citado 2024 nov. 13 ]
Vancouver
Zukerman-Schpector J, Maganhi SH, Olivato PR, Vinhato E, Cerqueira Júnior CR. Crystal structure of cis-4-tert-butyl-2-(4-nitrophenylsulfonyl)cyclohexanone, 'C IND. 16''H IND. 21''NO IND. 5'S. Zeitschrift für Kristallographie - New Crystal Structures. 2006 ; 221( 2): 165-166.[citado 2024 nov. 13 ]
Artigo de periodico
Surfactants with an amide group "spacer": synthesis of 3-(acylaminopropyl)trimethylammonium chlorides and their aggregation in aqueous solutions (2006)
Pires, Paulo Augusto Rodrigues; El Seoud, Omar A
Source: Journal of Colloid and Interface Science. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, SURFACTANTES, SOLUÇÕES AQUOSAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PIRES, Paulo Augusto Rodrigues e EL SEOUD, Omar A. Surfactants with an amide group "spacer": synthesis of 3-(acylaminopropyl)trimethylammonium chlorides and their aggregation in aqueous solutions. Journal of Colloid and Interface Science, v. 304, n. 2, p. 474-485, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jcis.2006.09.018. Acesso em: 13 nov. 2024.
APA
Pires, P. A. R., & El Seoud, O. A. (2006). Surfactants with an amide group "spacer": synthesis of 3-(acylaminopropyl)trimethylammonium chlorides and their aggregation in aqueous solutions. Journal of Colloid and Interface Science, 304( 2), 474-485. doi:10.1016/j.jcis.2006.09.018
NLM
Pires PAR, El Seoud OA. Surfactants with an amide group "spacer": synthesis of 3-(acylaminopropyl)trimethylammonium chlorides and their aggregation in aqueous solutions [Internet]. Journal of Colloid and Interface Science. 2006 ; 304( 2): 474-485.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.jcis.2006.09.018
Vancouver
Pires PAR, El Seoud OA. Surfactants with an amide group "spacer": synthesis of 3-(acylaminopropyl)trimethylammonium chlorides and their aggregation in aqueous solutions [Internet]. Journal of Colloid and Interface Science. 2006 ; 304( 2): 474-485.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.jcis.2006.09.018

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