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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: 15 dez. 2025.
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 2025 dez. 15 ] 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 2025 dez. 15 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
Artigo de periodico
The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction (2009)
Silva, Márcio S.; Santos, Alcindo Aparecido dos ; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
SILVA, Márcio S. e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters, v. 50, n. 47, p. 6498-6501, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.09.023. Acesso em: 15 dez. 2025.
APA
Silva, M. S., Santos, A. A. dos, & Comasseto, J. V. (2009). The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters, 50( 47), 6498-6501. doi:10.1016/j.tetlet.2009.09.023
NLM
Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.tetlet.2009.09.023
Vancouver
Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.tetlet.2009.09.023
Artigo de periodico
Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent (2009)
Andrade, Leandro Helgueira ; Piovan, Leandro; Pasquini, Mônica D`Arcadia
Source: Tetrahedron Asymmetry. Unidade: IQ
Subjects: ASPERGILLUS, QUÍMICA ORGÂNICA
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ABNT
ANDRADE, Leandro Helgueira e PIOVAN, Leandro e PASQUINI, Mônica D`Arcadia. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, v. 20, n. 13, p. 1521-1525, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.05.033. Acesso em: 15 dez. 2025.
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 2025 dez. 15 ] 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 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
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: 15 dez. 2025.
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 2025 dez. 15 ] 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 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
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: 15 dez. 2025.
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 2025 dez. 15 ] 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 2025 dez. 15 ] 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: 15 dez. 2025.
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 2025 dez. 15 ]
Vancouver
Ferraz HMC, Bombonato FI, Longo Junior LS. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis. 2007 ;( 21): 3261-3285.[citado 2025 dez. 15 ]
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: 15 dez. 2025.
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 2025 dez. 15 ] 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 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.tetlet.2007.07.054
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: 15 dez. 2025.
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 2025 dez. 15 ] 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 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039
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: 15 dez. 2025.
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 2025 dez. 15 ]
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 2025 dez. 15 ]
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
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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: 15 dez. 2025.
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 2025 dez. 15 ] 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 2025 dez. 15 ] 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: 15 dez. 2025.
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 2025 dez. 15 ] 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 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.014
Artigo de periodico
Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides (2006)
Dos Santos, Alcindo Aparecido; Da Costa, Carlos Eduardo; Princival, Jefferson Luiz; Comasseto, João Valdir
Source: Tetrahedron - Asymmetry. Unidade: IQ
Subjects: LIPASE, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 15 dez. 2025.
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 2025 dez. 15 ] 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 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.024
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: 15 dez. 2025.
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 2025 dez. 15 ] 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 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.tet.2006.06.051
Artigo de periodico
A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination (2006)
Gariani, Rogério Aparecido; Simonelli, Fabio; Oliveira, Alfredo Ricardo Marques de; Barison, Andersson; Comasseto, João Valdir
Source: Tetrahedron - Asymmetry. Unidade: IQ
Subjects: TELÚRIO, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GARIANI, Rogério Aparecido et al. A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination. Tetrahedron - Asymmetry, v. 17, n. 20, p. 2930-2934, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2006.10.034. Acesso em: 15 dez. 2025.
APA
Gariani, R. A., Simonelli, F., Oliveira, A. R. M. de, Barison, A., & Comasseto, J. V. (2006). A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination. Tetrahedron - Asymmetry, 17( 20), 2930-2934. doi:10.1016/j.tetasy.2006.10.034
NLM
Gariani RA, Simonelli F, Oliveira ARM de, Barison A, Comasseto JV. A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 20): 2930-2934.[citado 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.tetasy.2006.10.034
Vancouver
Gariani RA, Simonelli F, Oliveira ARM de, Barison A, Comasseto JV. A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 20): 2930-2934.[citado 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.tetasy.2006.10.034
Artigo de periodico
Highly stereoselective preparation of (3R,4S)-3,4-chromanediol by deracemization of (+-)-3-hydroxy-4-chromanone by Trichosporon cutaneum (2005)
Lunardi, Inês; Conceicao, Gelson Jose Andrade da; Moran, Paulo J. S.; Rodrigues, J A R
Source: Tetrahedron - Asymmetry. Unidade: FZEA
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LUNARDI, Inês et al. Highly stereoselective preparation of (3R,4S)-3,4-chromanediol by deracemization of (+-)-3-hydroxy-4-chromanone by Trichosporon cutaneum. Tetrahedron - Asymmetry, v. 16, n. 15, p. 2515-2519, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2005.06.020. Acesso em: 15 dez. 2025.
APA
Lunardi, I., Conceicao, G. J. A. da, Moran, P. J. S., & Rodrigues, J. A. R. (2005). Highly stereoselective preparation of (3R,4S)-3,4-chromanediol by deracemization of (+-)-3-hydroxy-4-chromanone by Trichosporon cutaneum. Tetrahedron - Asymmetry, 16( 15), 2515-2519. doi:10.1016/j.tetasy.2005.06.020
NLM
Lunardi I, Conceicao GJA da, Moran PJS, Rodrigues JAR. Highly stereoselective preparation of (3R,4S)-3,4-chromanediol by deracemization of (+-)-3-hydroxy-4-chromanone by Trichosporon cutaneum [Internet]. Tetrahedron - Asymmetry. 2005 ; 16( 15): 2515-2519.[citado 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.tetasy.2005.06.020
Vancouver
Lunardi I, Conceicao GJA da, Moran PJS, Rodrigues JAR. Highly stereoselective preparation of (3R,4S)-3,4-chromanediol by deracemization of (+-)-3-hydroxy-4-chromanone by Trichosporon cutaneum [Internet]. Tetrahedron - Asymmetry. 2005 ; 16( 15): 2515-2519.[citado 2025 dez. 15 ] Available from: https://doi.org/10.1016/j.tetasy.2005.06.020
Artigo de periodico
'gamma'-butyltelluro-2-butanol: a route to reactive 1,4-dianion intermediates (2005)
Princival, Jefferson Luiz; Barros, Simone Maria Goncalves de; Comasseto, João Valdir; Dos Santos, Alcindo Aparecido
Source: Tetrahedron Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, TELÚRIO, LÍTIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PRINCIVAL, Jefferson Luiz et al. 'gamma'-butyltelluro-2-butanol: a route to reactive 1,4-dianion intermediates. Tetrahedron Letters, v. 46, n. 26, p. 4423-4425, 2005Tradução . . Acesso em: 15 dez. 2025.
APA
Princival, J. L., Barros, S. M. G. de, Comasseto, J. V., & Dos Santos, A. A. (2005). 'gamma'-butyltelluro-2-butanol: a route to reactive 1,4-dianion intermediates. Tetrahedron Letters, 46( 26), 4423-4425.
NLM
Princival JL, Barros SMG de, Comasseto JV, Dos Santos AA. 'gamma'-butyltelluro-2-butanol: a route to reactive 1,4-dianion intermediates. Tetrahedron Letters. 2005 ; 46( 26): 4423-4425.[citado 2025 dez. 15 ]
Vancouver
Princival JL, Barros SMG de, Comasseto JV, Dos Santos AA. 'gamma'-butyltelluro-2-butanol: a route to reactive 1,4-dianion intermediates. Tetrahedron Letters. 2005 ; 46( 26): 4423-4425.[citado 2025 dez. 15 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 15 dez. 2025.
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 2025 dez. 15 ] 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 2025 dez. 15 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 15 dez. 2025.
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 2025 dez. 15 ] 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 2025 dez. 15 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 15 dez. 2025.
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 2025 dez. 15 ]
Vancouver
Castelani P, Comasseto JV. Diastereoselective synthesis of 'alpha','beta'-unsaturated systems. Tetrahedron. 2005 ; 61( 9): 2319-2326.[citado 2025 dez. 15 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 15 dez. 2025.
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 2025 dez. 15 ]
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 2025 dez. 15 ]

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