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Artigo de periodico
A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients (2012)
Belsito, D; Bickers, D; Bruze, M; Calow, Peter; Dagli, Maria Lúcia Zaidan; Fryer, A. D; Greim, Helmut; Miyachi, Y; Saurat, J. H; Sipes, I. G
Source: Food and Chemical Toxicology. Unidade: FMVZ
Subjects: QUÍMICA ORGÂNICA, DERMATOLOGIA, TOXICOLOGIA
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ABNT
BELSITO, D et al. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients. Food and Chemical Toxicology, v. 50, p. S52-S99, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2011.10.042. Acesso em: 07 jul. 2024.
APA
Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2012). A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients. Food and Chemical Toxicology, 50, S52-S99. doi:10.1016/j.fct.2011.10.042
NLM
Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S52-S99.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.fct.2011.10.042
Vancouver
Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S52-S99.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.fct.2011.10.042
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: 07 jul. 2024.
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 2024 jul. 07 ] 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 2024 jul. 07 ] 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: 07 jul. 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 jul. 07 ] 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 jul. 07 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
Artigo de periodico
Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones (2009)
Princival, Jefferson Luiz; Santos, Alcindo Aparecido dos ; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Subjects: COMPOSTOS ORGANOMETÁLICOS, QUÍMICA ORGÂNICA
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ABNT
PRINCIVAL, Jefferson Luiz e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones. Tetrahedron Letters, v. 46, p. 6368-6371, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.08.097. Acesso em: 07 jul. 2024.
APA
Princival, J. L., Santos, A. A. dos, & Comasseto, J. V. (2009). Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones. Tetrahedron Letters, 46, 6368-6371. doi:10.1016/j.tetlet.2009.08.097
NLM
Princival JL, Santos AA dos, Comasseto JV. Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones [Internet]. Tetrahedron Letters. 2009 ; 46 6368-6371.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2009.08.097
Vancouver
Princival JL, Santos AA dos, Comasseto JV. Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones [Internet]. Tetrahedron Letters. 2009 ; 46 6368-6371.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2009.08.097
Artigo de periodico
Biotransformations on organic selenides and tellurides: synthetic applications (2009)
Comasseto, João Valdir; Gariani, Rogério Aparecido
Source: Tetrahedron. Unidade: IQ
Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA
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ABNT
COMASSETO, João Valdir e GARIANI, Rogério Aparecido. Biotransformations on organic selenides and tellurides: synthetic applications. Tetrahedron, v. 65, n. 41, p. 8447-8459, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2009.06.121. Acesso em: 07 jul. 2024.
APA
Comasseto, J. V., & Gariani, R. A. (2009). Biotransformations on organic selenides and tellurides: synthetic applications. Tetrahedron, 65( 41), 8447-8459. doi:10.1016/j.tet.2009.06.121
NLM
Comasseto JV, Gariani RA. Biotransformations on organic selenides and tellurides: synthetic applications [Internet]. Tetrahedron. 2009 ; 65( 41): 8447-8459.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tet.2009.06.121
Vancouver
Comasseto JV, Gariani RA. Biotransformations on organic selenides and tellurides: synthetic applications [Internet]. Tetrahedron. 2009 ; 65( 41): 8447-8459.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tet.2009.06.121
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: 07 jul. 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 jul. 07 ]
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 jul. 07 ]
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: 07 jul. 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 jul. 07 ] 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 jul. 07 ] Available from: https://doi.org/10.1016/j.bmcl.2007.10.068
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: 07 jul. 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 jul. 07 ] 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 jul. 07 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
Artigo de periodico
Antitumor activity of extracts from Peperomia elongata (2007)
Campos, Patricia Bonavides de Castro; Gama, Juliana Julian Torres; Pereira, Lícia Pacheco; Lotufo, Leticia Veras Costa ; Moraes, Manoel Odorico de; Guimarães, Elsie Franklin; Kato, Massuo Jorge ; Furlan, Maysa; Pessoa, Claudia
Source: Pharmaceutical Biology. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, PRODUTOS NATURAIS
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ABNT
CAMPOS, Patricia Bonavides de Castro et al. Antitumor activity of extracts from Peperomia elongata. Pharmaceutical Biology, v. 45, n. 10, p. 760-765, 2007Tradução . . Acesso em: 07 jul. 2024.
APA
Campos, P. B. de C., Gama, J. J. T., Pereira, L. P., Lotufo, L. V. C., Moraes, M. O. de, Guimarães, E. F., et al. (2007). Antitumor activity of extracts from Peperomia elongata. Pharmaceutical Biology, 45( 10), 760-765.
NLM
Campos PB de C, Gama JJT, Pereira LP, Lotufo LVC, Moraes MO de, Guimarães EF, Kato MJ, Furlan M, Pessoa C. Antitumor activity of extracts from Peperomia elongata. Pharmaceutical Biology. 2007 ; 45( 10): 760-765.[citado 2024 jul. 07 ]
Vancouver
Campos PB de C, Gama JJT, Pereira LP, Lotufo LVC, Moraes MO de, Guimarães EF, Kato MJ, Furlan M, Pessoa C. Antitumor activity of extracts from Peperomia elongata. Pharmaceutical Biology. 2007 ; 45( 10): 760-765.[citado 2024 jul. 07 ]
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: 07 jul. 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 jul. 07 ] 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 jul. 07 ] 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: 07 jul. 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 jul. 07 ] 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 jul. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2007.09.111
Artigo de periodico
Biosynthetic origins of the isoprene units of gaudichaudianic acid in Piper gaudichaudianum (Piperaceae) (2007)
Lopes, Adriana Aparecida; Baldoqui, Debora Cristina; López, Silvia Noelí; Kato, Massuo Jorge ; Bolzani, Vanderlan da Silva; Furlan, Maysa
Source: Phytochemistry. Unidade: IQ
Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA
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ABNT
LOPES, Adriana Aparecida et al. Biosynthetic origins of the isoprene units of gaudichaudianic acid in Piper gaudichaudianum (Piperaceae). Phytochemistry, v. 68, n. 15, p. 2053-2058, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.phytochem.2007.04.025. Acesso em: 07 jul. 2024.
APA
Lopes, A. A., Baldoqui, D. C., López, S. N., Kato, M. J., Bolzani, V. da S., & Furlan, M. (2007). Biosynthetic origins of the isoprene units of gaudichaudianic acid in Piper gaudichaudianum (Piperaceae). Phytochemistry, 68( 15), 2053-2058. doi:10.1016/j.phytochem.2007.04.025
NLM
Lopes AA, Baldoqui DC, López SN, Kato MJ, Bolzani V da S, Furlan M. Biosynthetic origins of the isoprene units of gaudichaudianic acid in Piper gaudichaudianum (Piperaceae) [Internet]. Phytochemistry. 2007 ; 68( 15): 2053-2058.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.phytochem.2007.04.025
Vancouver
Lopes AA, Baldoqui DC, López SN, Kato MJ, Bolzani V da S, Furlan M. Biosynthetic origins of the isoprene units of gaudichaudianic acid in Piper gaudichaudianum (Piperaceae) [Internet]. Phytochemistry. 2007 ; 68( 15): 2053-2058.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.phytochem.2007.04.025
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 07 jul. 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 jul. 07 ] 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 jul. 07 ] 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: 07 jul. 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 jul. 07 ] 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 jul. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039
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: 07 jul. 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 jul. 07 ] 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 jul. 07 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.024
Artigo de periodico
Chromenes from Peperomia serpens (Sw.) Loudon (Piperaceae) (2006)
Kitamura, Rodrigo Ossamu Saga; Romoff, Paulete; Young, Maria Claudia Marx; Kato, Massuo Jorge ; Lago, João Henrique Ghilardi
Source: Phytochemistry. Unidade: IQ
Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KITAMURA, Rodrigo Ossamu Saga et al. Chromenes from Peperomia serpens (Sw.) Loudon (Piperaceae). Phytochemistry, v. 67, n. 21, p. 2398-2402, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.phytochem.2006.08.007. Acesso em: 07 jul. 2024.
APA
Kitamura, R. O. S., Romoff, P., Young, M. C. M., Kato, M. J., & Lago, J. H. G. (2006). Chromenes from Peperomia serpens (Sw.) Loudon (Piperaceae). Phytochemistry, 67( 21), 2398-2402. doi:10.1016/j.phytochem.2006.08.007
NLM
Kitamura ROS, Romoff P, Young MCM, Kato MJ, Lago JHG. Chromenes from Peperomia serpens (Sw.) Loudon (Piperaceae) [Internet]. Phytochemistry. 2006 ; 67( 21): 2398-2402.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.phytochem.2006.08.007
Vancouver
Kitamura ROS, Romoff P, Young MCM, Kato MJ, Lago JHG. Chromenes from Peperomia serpens (Sw.) Loudon (Piperaceae) [Internet]. Phytochemistry. 2006 ; 67( 21): 2398-2402.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.phytochem.2006.08.007
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: 07 jul. 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 jul. 07 ] 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 jul. 07 ] 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: 07 jul. 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 jul. 07 ] 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 jul. 07 ] 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: 07 jul. 2024.
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 2024 jul. 07 ] 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 2024 jul. 07 ] 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: 07 jul. 2024.
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 2024 jul. 07 ] 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 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tetasy.2005.06.020

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