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Artigo de periodico
Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides (2009)
Stefani, Hélio Alexandre ; Pena, Jesus Marcelo; Gueogjian, Kemilla; Petragnani, Nicola; Vaz, Boniek Gontijo; Eberlin, Marcos Nogueira
Source: Tetrahedron Letters. Unidades: FCF, IQ
Subjects: SÍNTESE ORGÂNICA, TELÚRIO, PALÁDIO
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ABNT
STEFANI, Hélio Alexandre et al. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, v. 50, n. 40, p. 5589-5595, 2009Tradução . . Acesso em: 04 out. 2024.
APA
Stefani, H. A., Pena, J. M., Gueogjian, K., Petragnani, N., Vaz, B. G., & Eberlin, M. N. (2009). Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, 50( 40), 5589-5595.
NLM
Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 out. 04 ]
Vancouver
Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 out. 04 ]
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: 04 out. 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 out. 04 ] 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 out. 04 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
Artigo de periodico
Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds (2009)
Keppler, Artur Franz; Gariani, Rogério Aparecido; Lopes, Danilo G.; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Subjects: LÍTIO, CALCOGÊNIOS, SÍNTESE ORGÂNICA
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ABNT
KEPPLER, Artur Franz et al. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds. Tetrahedron Letters, v. 50, n. 19, p. 2181-2184, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.02.158. Acesso em: 04 out. 2024.
APA
Keppler, A. F., Gariani, R. A., Lopes, D. G., & Comasseto, J. V. (2009). Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds. Tetrahedron Letters, 50( 19), 2181-2184. doi:10.1016/j.tetlet.2009.02.158
NLM
Keppler AF, Gariani RA, Lopes DG, Comasseto JV. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds [Internet]. Tetrahedron Letters. 2009 ; 50( 19): 2181-2184.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
Vancouver
Keppler AF, Gariani RA, Lopes DG, Comasseto JV. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds [Internet]. Tetrahedron Letters. 2009 ; 50( 19): 2181-2184.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
Artigo de periodico
First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B) (2009)
Andrade, Leandro Helgueira ; Silva, Alexandre Vieira; Pedrozo, Eliane Correa
Source: Tetrahedron Letters. Unidade: IQ
Subjects: PALÁDIO, CANDIDA
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ABNT
ANDRADE, Leandro Helgueira e SILVA, Alexandre Vieira e PEDROZO, Eliane Correa. First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B). Tetrahedron Letters, v. 50, n. 30, p. 4331-4334, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.05.022. Acesso em: 04 out. 2024.
APA
Andrade, L. H., Silva, A. V., & Pedrozo, E. C. (2009). First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B). Tetrahedron Letters, 50( 30), 4331-4334. doi:10.1016/j.tetlet.2009.05.022
NLM
Andrade LH, Silva AV, Pedrozo EC. First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B) [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4331-4334.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2009.05.022
Vancouver
Andrade LH, Silva AV, Pedrozo EC. First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B) [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4331-4334.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2009.05.022
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: 04 out. 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 out. 04 ]
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 out. 04 ]
Artigo de periodico
'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters (2008)
Proti, Patrícia Barrientos; Miranda, Maria Terêsa Machini de
Source: Tetrahedron Letters. Unidade: IQ
Subjects: PROTEÍNAS, BIOQUÍMICA, PEPTÍDEOS (SÍNTESE)
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ABNT
PROTI, Patrícia Barrientos e MIRANDA, Maria Terêsa Machini de. 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters, v. 49, n. 24, p. 3853-3857, 2008Tradução . . Acesso em: 04 out. 2024.
APA
Proti, P. B., & Miranda, M. T. M. de. (2008). 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters, 49( 24), 3853-3857.
NLM
Proti PB, Miranda MTM de. 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters. 2008 ;49( 24): 3853-3857.[citado 2024 out. 04 ]
Vancouver
Proti PB, Miranda MTM de. 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters. 2008 ;49( 24): 3853-3857.[citado 2024 out. 04 ]
Artigo de periodico
Tellurium tetrachloride: an improved method of preparation (2008)
Petragnani, Nicola; Mendes, Samuel Rodrigues; Silveira, Claudio da Cruz
Source: Tetrahedron Letters. Unidade: IQ
Subjects: TELÚRIO, REAGENTES ORGÂNICOS
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ABNT
PETRAGNANI, Nicola e MENDES, Samuel Rodrigues e SILVEIRA, Claudio da Cruz. Tellurium tetrachloride: an improved method of preparation. Tetrahedron Letters, v. 49, n. 15, p. 2371-2372, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.02.085. Acesso em: 04 out. 2024.
APA
Petragnani, N., Mendes, S. R., & Silveira, C. da C. (2008). Tellurium tetrachloride: an improved method of preparation. Tetrahedron Letters, 49( 15), 2371-2372. doi:10.1016/j.tetlet.2008.02.085
NLM
Petragnani N, Mendes SR, Silveira C da C. Tellurium tetrachloride: an improved method of preparation [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2371-2372.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.085
Vancouver
Petragnani N, Mendes SR, Silveira C da C. Tellurium tetrachloride: an improved method of preparation [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2371-2372.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.085
Artigo de periodico
Synthesis of the C7-C24 fragment of (-)-Macrolactin F (2008)
Oliveira, Roberta A.; Oliveira, Juliana M.; Rahmeier, L. H. S.; Comasseto, João Valdir; Marino, Joseph P.; Menezes, Paulo Henrique
Source: Tetrahedron Letters. Unidade: IQ
Subjects: REAGENTES ORGÂNICOS, TELÚRIO
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ABNT
OLIVEIRA, Roberta A. et al. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters, v. 49, n. 40, p. 5759-5761, 2008Tradução . . Acesso em: 04 out. 2024.
APA
Oliveira, R. A., Oliveira, J. M., Rahmeier, L. H. S., Comasseto, J. V., Marino, J. P., & Menezes, P. H. (2008). Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters, 49( 40), 5759-5761.
NLM
Oliveira RA, Oliveira JM, Rahmeier LHS, Comasseto JV, Marino JP, Menezes PH. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters. 2008 ; 49( 40): 5759-5761.[citado 2024 out. 04 ]
Vancouver
Oliveira RA, Oliveira JM, Rahmeier LHS, Comasseto JV, Marino JP, Menezes PH. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters. 2008 ; 49( 40): 5759-5761.[citado 2024 out. 04 ]
Artigo de periodico
First chemoenzymatic synthesis of organoselenium amines and amides (2008)
Andrade, Leandro Helgueira ; Silva, Alexandre Vieira
Source: Tetrahedron - Asymmetry. Unidade: IQ
Subjects: AMINAS (COMPOSTOS ORGÂNICOS), REAGENTES ORGÂNICOS
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ABNT
ANDRADE, Leandro Helgueira e SILVA, Alexandre Vieira. First chemoenzymatic synthesis of organoselenium amines and amides. Tetrahedron - Asymmetry, v. 19, n. 10, p. 1175-1181, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2008.04.026. Acesso em: 04 out. 2024.
APA
Andrade, L. H., & Silva, A. V. (2008). First chemoenzymatic synthesis of organoselenium amines and amides. Tetrahedron - Asymmetry, 19( 10), 1175-1181. doi:10.1016/j.tetasy.2008.04.026
NLM
Andrade LH, Silva AV. First chemoenzymatic synthesis of organoselenium amines and amides [Internet]. Tetrahedron - Asymmetry. 2008 ;19( 10): 1175-1181.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetasy.2008.04.026
Vancouver
Andrade LH, Silva AV. First chemoenzymatic synthesis of organoselenium amines and amides [Internet]. Tetrahedron - Asymmetry. 2008 ;19( 10): 1175-1181.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetasy.2008.04.026
Artigo de periodico
Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives (2008)
Toledo, Fabiano Travanca; Cunha, Rodrigo Luiz Oliveira Rodrigues; Raminelli, Cristiano; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS
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ABNT
TOLEDO, Fabiano Travanca et al. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives. Tetrahedron Letters, v. 49, n. 5, p. 873-875, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.11.169. Acesso em: 04 out. 2024.
APA
Toledo, F. T., Cunha, R. L. O. R., Raminelli, C., & Comasseto, J. V. (2008). Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives. Tetrahedron Letters, 49( 5), 873-875. doi:10.1016/j.tetlet.2007.11.169
NLM
Toledo FT, Cunha RLOR, Raminelli C, Comasseto JV. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives [Internet]. Tetrahedron Letters. 2008 ;49( 5): 873-875.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.169
Vancouver
Toledo FT, Cunha RLOR, Raminelli C, Comasseto JV. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives [Internet]. Tetrahedron Letters. 2008 ;49( 5): 873-875.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.169
Artigo de periodico
Tellurium in organic synthesis: synthesis of bioactive butenolides (2007)
Bassora, Bruno Karaski; Da Costa, Carlos Eduardo; Gariani, Rogério Aparecido; Comasseto, João Valdir; Dos Santos, Alcindo Aparecido
Source: Tetrahedron Letters. Unidade: IQ
Subjects: TELÚRIO, SÍNTESE ORGÂNICA
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ABNT
BASSORA, Bruno Karaski et al. Tellurium in organic synthesis: synthesis of bioactive butenolides. Tetrahedron Letters, v. 48, n. 8, p. 1485-1487, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.12.063. Acesso em: 04 out. 2024.
APA
Bassora, B. K., Da Costa, C. E., Gariani, R. A., Comasseto, J. V., & Dos Santos, A. A. (2007). Tellurium in organic synthesis: synthesis of bioactive butenolides. Tetrahedron Letters, 48( 8), 1485-1487. doi:10.1016/j.tetlet.2006.12.063
NLM
Bassora BK, Da Costa CE, Gariani RA, Comasseto JV, Dos Santos AA. Tellurium in organic synthesis: synthesis of bioactive butenolides [Internet]. Tetrahedron Letters. 2007 ; 48( 8): 1485-1487.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2006.12.063
Vancouver
Bassora BK, Da Costa CE, Gariani RA, Comasseto JV, Dos Santos AA. Tellurium in organic synthesis: synthesis of bioactive butenolides [Internet]. Tetrahedron Letters. 2007 ; 48( 8): 1485-1487.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2006.12.063
Artigo de periodico
Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 (2007)
Omori, Álvaro Takeo; Assis, Leonardo Fernandes; Andrade, Leandro Helgueira ; Comasseto, João Valdir; Porto, Andre Luiz Meleiro
Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC
Subjects: CANDIDA, SÍNTESE ORGÂNICA, ASPERGILLUS
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ABNT
OMORI, Álvaro Takeo et al. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435. Tetrahedron - Asymmetry, v. 18, n. 9, p. 1048-1053, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2007.04.019. Acesso em: 04 out. 2024.
APA
Omori, Á. T., Assis, L. F., Andrade, L. H., Comasseto, J. V., & Porto, A. L. M. (2007). Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435. Tetrahedron - Asymmetry, 18( 9), 1048-1053. doi:10.1016/j.tetasy.2007.04.019
NLM
Omori ÁT, Assis LF, Andrade LH, Comasseto JV, Porto ALM. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1048-1053.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
Vancouver
Omori ÁT, Assis LF, Andrade LH, Comasseto JV, Porto ALM. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1048-1053.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
Artigo de periodico
The coupling of butylvinyltellurides with organometallic reagents catalysed by nickel complexes (2007)
Raminelli, Cristiano; Gargalaka Júnior, João; Silveira, Cláudio da Cruz; Comasseto, João Valdir
Source: Tetrahedron. Unidade: IQ
Subjects: CATÁLISE, REAGENTES ORGÂNICOS
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ABNT
RAMINELLI, Cristiano et al. The coupling of butylvinyltellurides with organometallic reagents catalysed by nickel complexes. Tetrahedron, v. 63, n. 36, p. 8801-8809, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2007.06.057. Acesso em: 04 out. 2024.
APA
Raminelli, C., Gargalaka Júnior, J., Silveira, C. da C., & Comasseto, J. V. (2007). The coupling of butylvinyltellurides with organometallic reagents catalysed by nickel complexes. Tetrahedron, 63( 36), 8801-8809. doi:10.1016/j.tet.2007.06.057
NLM
Raminelli C, Gargalaka Júnior J, Silveira C da C, Comasseto JV. The coupling of butylvinyltellurides with organometallic reagents catalysed by nickel complexes [Internet]. Tetrahedron. 2007 ; 63( 36): 8801-8809.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tet.2007.06.057
Vancouver
Raminelli C, Gargalaka Júnior J, Silveira C da C, Comasseto JV. The coupling of butylvinyltellurides with organometallic reagents catalysed by nickel complexes [Internet]. Tetrahedron. 2007 ; 63( 36): 8801-8809.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tet.2007.06.057
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 04 out. 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 out. 04 ] 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 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2007.09.111
Artigo de periodico
Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation (2007)
Ferraz, Helena Maria Carvalho; Bianco, Graziela Gallego; Teixeira, Carla C.; Andrade, Leandro Helgueira ; Porto, Andre Luiz Meleiro
Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC
Subjects: CANDIDA, HIDROGENAÇÃO, LIPASE
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ABNT
FERRAZ, Helena Maria Carvalho et al. Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation. Tetrahedron - Asymmetry, v. 18, n. 9, p. 1070-1076, 2007Tradução . . Acesso em: 04 out. 2024.
APA
Ferraz, H. M. C., Bianco, G. G., Teixeira, C. C., Andrade, L. H., & Porto, A. L. M. (2007). Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation. Tetrahedron - Asymmetry, 18( 9), 1070-1076.
NLM
Ferraz HMC, Bianco GG, Teixeira CC, Andrade LH, Porto ALM. Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1070-1076.[citado 2024 out. 04 ]
Vancouver
Ferraz HMC, Bianco GG, Teixeira CC, Andrade LH, Porto ALM. Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1070-1076.[citado 2024 out. 04 ]
Artigo de periodico
Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435) (2007)
Reigada, Juliana Beltrame; Tcacenco, Celize Maia; Andrade, Leandro Helgueira ; Kato, Massuo Jorge ; Porto, Andre Luiz Meleiro ; Lago, João Henrique Ghilardi
Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC
Subjects: ANTIFÚNGICOS (ATIVIDADE), CANDIDA, PRODUTOS NATURAIS
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ABNT
REIGADA, Juliana Beltrame et al. Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, v. 18, n. 9, p. 1054-1058, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2007.05.006. Acesso em: 04 out. 2024.
APA
Reigada, J. B., Tcacenco, C. M., Andrade, L. H., Kato, M. J., Porto, A. L. M., & Lago, J. H. G. (2007). Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, 18( 9), 1054-1058. doi:10.1016/j.tetasy.2007.05.006
NLM
Reigada JB, Tcacenco CM, Andrade LH, Kato MJ, Porto ALM, Lago JHG. Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1054-1058.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.006
Vancouver
Reigada JB, Tcacenco CM, Andrade LH, Kato MJ, Porto ALM, Lago JHG. Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1054-1058.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.006
Artigo de periodico
Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems (2007)
Dos Santos, Alcindo Aparecido; Princival, Jefferson Luiz; Comasseto, João Valdir; Barros, Simone Maria Goncalves de; Brainer Neto, José Eustáquio
Source: Tetrahedron. Unidade: IQ
Subjects: TELÚRIO, LÍTIO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DOS SANTOS, Alcindo Aparecido et al. Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems. Tetrahedron, v. 63, n. 24, p. 5167-5172, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2007.03.178. Acesso em: 04 out. 2024.
APA
Dos Santos, A. A., Princival, J. L., Comasseto, J. V., Barros, S. M. G. de, & Brainer Neto, J. E. (2007). Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems. Tetrahedron, 63( 24), 5167-5172. doi:10.1016/j.tet.2007.03.178
NLM
Dos Santos AA, Princival JL, Comasseto JV, Barros SMG de, Brainer Neto JE. Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems [Internet]. Tetrahedron. 2007 ; 63( 24): 5167-5172.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tet.2007.03.178
Vancouver
Dos Santos AA, Princival JL, Comasseto JV, Barros SMG de, Brainer Neto JE. Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems [Internet]. Tetrahedron. 2007 ; 63( 24): 5167-5172.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tet.2007.03.178
Artigo de periodico
Stereoselective synthesis of vinylic chalcogenides through vinylic substitution by lithium organylchalcogenolates (2007)
Silveira, Claudio da Cruz; Guerra, Robson Brum; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Subjects: LÍTIO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVEIRA, Claudio da Cruz e GUERRA, Robson Brum e COMASSETO, João Valdir. Stereoselective synthesis of vinylic chalcogenides through vinylic substitution by lithium organylchalcogenolates. Tetrahedron Letters, v. 48, n. 29, p. 5121-5124, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.05.074. Acesso em: 04 out. 2024.
APA
Silveira, C. da C., Guerra, R. B., & Comasseto, J. V. (2007). Stereoselective synthesis of vinylic chalcogenides through vinylic substitution by lithium organylchalcogenolates. Tetrahedron Letters, 48( 29), 5121-5124. doi:10.1016/j.tetlet.2007.05.074
NLM
Silveira C da C, Guerra RB, Comasseto JV. Stereoselective synthesis of vinylic chalcogenides through vinylic substitution by lithium organylchalcogenolates [Internet]. Tetrahedron Letters. 2007 ; 48( 29): 5121-5124.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2007.05.074
Vancouver
Silveira C da C, Guerra RB, Comasseto JV. Stereoselective synthesis of vinylic chalcogenides through vinylic substitution by lithium organylchalcogenolates [Internet]. Tetrahedron Letters. 2007 ; 48( 29): 5121-5124.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2007.05.074
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: 04 out. 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 out. 04 ] 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 out. 04 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 04 out. 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 out. 04 ] 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 out. 04 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039

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