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Artigo de periodico
Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol (2017)
Lima, Rafaely Nascimento; Porto, Andre Luiz Meleiro
Source: Tetrahedron. Unidade: IQSC
Assunto: QUÍMICA VERDE
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ABNT
LIMA, Rafaely Nascimento e PORTO, Andre Luiz Meleiro. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol. Tetrahedron, v. 58, n. 9, p. 825-828, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.12.062. Acesso em: 11 maio 2024.
APA
Lima, R. N., & Porto, A. L. M. (2017). Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol. Tetrahedron, 58( 9), 825-828. doi:10.1016/j.tetlet.2016.12.062
NLM
Lima RN, Porto ALM. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol [Internet]. Tetrahedron. 2017 ; 58( 9): 825-828.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetlet.2016.12.062
Vancouver
Lima RN, Porto ALM. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol [Internet]. Tetrahedron. 2017 ; 58( 9): 825-828.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetlet.2016.12.062
Artigo de periodico
Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 (2016)
Jimenez, David Esteban Quintero; Ferreira , Irlon Maciel; Birolli, Willian Garcia; Fonseca, Luis P.; Porto, Andre Luiz Meleiro
Source: Tetrahedron. Unidade: IQSC
Subjects: FUNGOS, QUÍMICA ORGÂNICA
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ABNT
JIMENEZ, David Esteban Quintero et al. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, v. 72, n. 46, p. 7317-7322, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2016.02.014. Acesso em: 11 maio 2024.
APA
Jimenez, D. E. Q., Ferreira , I. M., Birolli, W. G., Fonseca, L. P., & Porto, A. L. M. (2016). Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, 72( 46), 7317-7322. doi:10.1016/j.tet.2016.02.014
NLM
Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tet.2016.02.014
Vancouver
Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tet.2016.02.014
Trabalho de evento-resumo
Biotransformation of organophjosphate pesticides by marine fungy (2013)
Silva, Natália Alvarenga da; Seleghim, Mirna Helena Regali; Porto, Andre Luiz Meleiro
Source: Book of abstracts. Conference titles: BIOTRANS 2013. Unidade: IQSC
Subjects: BIOTRANSFORMAÇÃO, PESTICIDAS
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ABNT
SILVA, Natália Alvarenga da e SELEGHIM, Mirna Helena Regali e PORTO, Andre Luiz Meleiro. Biotransformation of organophjosphate pesticides by marine fungy. 2013, Anais.. Manchester: Instituto de Química de São Carlos, Universidade de São Paulo, 2013. Disponível em: https://repositorio.usp.br/directbitstream/2d6fb913-f582-4173-b840-226eb870751c/P14450.pdf. Acesso em: 11 maio 2024.
APA
Silva, N. A. da, Seleghim, M. H. R., & Porto, A. L. M. (2013). Biotransformation of organophjosphate pesticides by marine fungy. In Book of abstracts. Manchester: Instituto de Química de São Carlos, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/2d6fb913-f582-4173-b840-226eb870751c/P14450.pdf
NLM
Silva NA da, Seleghim MHR, Porto ALM. Biotransformation of organophjosphate pesticides by marine fungy [Internet]. Book of abstracts. 2013 ;[citado 2024 maio 11 ] Available from: https://repositorio.usp.br/directbitstream/2d6fb913-f582-4173-b840-226eb870751c/P14450.pdf
Vancouver
Silva NA da, Seleghim MHR, Porto ALM. Biotransformation of organophjosphate pesticides by marine fungy [Internet]. Book of abstracts. 2013 ;[citado 2024 maio 11 ] Available from: https://repositorio.usp.br/directbitstream/2d6fb913-f582-4173-b840-226eb870751c/P14450.pdf
Artigo de periodico
Kinetic resolution of iodophenylethanols by candida antarctica lipase and their application for the synthesis of chiral biphenyl compounds (2010)
Rocha, Lenilson Coutinho da; Rosset, Isac G; Luiz, Rodrigo Pereira; Raminelli, Cristiano; Porto, Andre Luiz Meleiro
Source: Tetrahedron: Asymmetry. Unidade: IQSC
Assunto: QUÍMICA
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ABNT
ROCHA, Lenilson Coutinho da et al. Kinetic resolution of iodophenylethanols by candida antarctica lipase and their application for the synthesis of chiral biphenyl compounds. Tetrahedron: Asymmetry, v. 21, n. 8, p. 926-929, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2010.05.008. Acesso em: 11 maio 2024.
APA
Rocha, L. C. da, Rosset, I. G., Luiz, R. P., Raminelli, C., & Porto, A. L. M. (2010). Kinetic resolution of iodophenylethanols by candida antarctica lipase and their application for the synthesis of chiral biphenyl compounds. Tetrahedron: Asymmetry, 21( 8), 926-929. doi:10.1016/j.tetasy.2010.05.008
NLM
Rocha LC da, Rosset IG, Luiz RP, Raminelli C, Porto ALM. Kinetic resolution of iodophenylethanols by candida antarctica lipase and their application for the synthesis of chiral biphenyl compounds [Internet]. Tetrahedron: Asymmetry. 2010 ; 21( 8): 926-929.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2010.05.008
Vancouver
Rocha LC da, Rosset IG, Luiz RP, Raminelli C, Porto ALM. Kinetic resolution of iodophenylethanols by candida antarctica lipase and their application for the synthesis of chiral biphenyl compounds [Internet]. Tetrahedron: Asymmetry. 2010 ; 21( 8): 926-929.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2010.05.008
Artigo de periodico
First stereocontrolled acetylation of a hydroxypropargylpiperidone by lipase CALB (2010)
Melgar, Gilseida Zelayarán; Wendler, Edison P; Santos, Alcindo Aparecido dos ; Porto, Andre Luiz Meleiro
Source: Tetrahedron: Asymmetry. Unidades: IQSC, IQ
Assunto: QUÍMICA
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ABNT
MELGAR, Gilseida Zelayarán et al. First stereocontrolled acetylation of a hydroxypropargylpiperidone by lipase CALB. Tetrahedron: Asymmetry, v. 21, n. 8, p. 2271-2274, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2010.07.024. Acesso em: 11 maio 2024.
APA
Melgar, G. Z., Wendler, E. P., Santos, A. A. dos, & Porto, A. L. M. (2010). First stereocontrolled acetylation of a hydroxypropargylpiperidone by lipase CALB. Tetrahedron: Asymmetry, 21( 8), 2271-2274. doi:10.1016/j.tetasy.2010.07.024
NLM
Melgar GZ, Wendler EP, Santos AA dos, Porto ALM. First stereocontrolled acetylation of a hydroxypropargylpiperidone by lipase CALB [Internet]. Tetrahedron: Asymmetry. 2010 ; 21( 8): 2271-2274.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2010.07.024
Vancouver
Melgar GZ, Wendler EP, Santos AA dos, Porto ALM. First stereocontrolled acetylation of a hydroxypropargylpiperidone by lipase CALB [Internet]. Tetrahedron: Asymmetry. 2010 ; 21( 8): 2271-2274.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2010.07.024
Artigo de periodico
Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms (2008)
Piovan, Leandro; Kagohara, Edna; Ricci, Luís C.; Keppler, Artur F.; Capelari, Marina; Andrade, Leandro Helgueira ; Comasseto, João Valdir; Porto, Andre Luiz Meleiro
Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC
Subjects: QUÍMICA, CÉLULAS
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ABNT
PIOVAN, Leandro et al. Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms. Tetrahedron - Asymmetry, v. 19, n. 20, p. 2385-2389, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2008.10.003. Acesso em: 11 maio 2024.
APA
Piovan, L., Kagohara, E., Ricci, L. C., Keppler, A. F., Capelari, M., Andrade, L. H., et al. (2008). Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms. Tetrahedron - Asymmetry, 19( 20), 2385-2389. doi:10.1016/j.tetasy.2008.10.003
NLM
Piovan L, Kagohara E, Ricci LC, Keppler AF, Capelari M, Andrade LH, Comasseto JV, Porto ALM. Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms [Internet]. Tetrahedron - Asymmetry. 2008 ; 19( 20): 2385-2389.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2008.10.003
Vancouver
Piovan L, Kagohara E, Ricci LC, Keppler AF, Capelari M, Andrade LH, Comasseto JV, Porto ALM. Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms [Internet]. Tetrahedron - Asymmetry. 2008 ; 19( 20): 2385-2389.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2008.10.003
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: 11 maio 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 maio 11 ] 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 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
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: 11 maio 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 maio 11 ]
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 maio 11 ]
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: 11 maio 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 maio 11 ] 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 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.006
Artigo de periodico
Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes (2007)
Piovan, Leandro; Capelari, Marina; Andrade, Leandro Helgueira ; Comasseto, João Valdir; Porto, Andre Luiz Meleiro
Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC
Subjects: BOTÂNICA, QUÍMICA
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ABNT
PIOVAN, Leandro et al. Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes. Tetrahedron - Asymmetry, v. 18, n. 12, p. 1398-1402, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2007.05.036. Acesso em: 11 maio 2024.
APA
Piovan, L., Capelari, M., Andrade, L. H., Comasseto, J. V., & Porto, A. L. M. (2007). Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes. Tetrahedron - Asymmetry, 18( 12), 1398-1402. doi:10.1016/j.tetasy.2007.05.036
NLM
Piovan L, Capelari M, Andrade LH, Comasseto JV, Porto ALM. Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 12): 1398-1402.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.036
Vancouver
Piovan L, Capelari M, Andrade LH, Comasseto JV, Porto ALM. Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 12): 1398-1402.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.036
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
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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: 11 maio 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 maio 11 ] 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 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.014
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: 11 maio 2024.
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 2024 maio 11 ] 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 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tet.2004.10.087
Artigo de periodico
Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435) (2004)
Raminelli, Cristiano; Comasseto, João Valdir; Andrade, Leandro Helgueira ; Porto, Andre Luiz Meleiro
Source: Tetrahedron - Asymmetry. Unidade: IQ
Subjects: QUÍMICA FINA, CANDIDA, LIPASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMINELLI, Cristiano et al. Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435). Tetrahedron - Asymmetry, v. 15, n. 19, p. 3117-3122, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2004.08.022. Acesso em: 11 maio 2024.
APA
Raminelli, C., Comasseto, J. V., Andrade, L. H., & Porto, A. L. M. (2004). Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435). Tetrahedron - Asymmetry, 15( 19), 3117-3122. doi:10.1016/j.tetasy.2004.08.022
NLM
Raminelli C, Comasseto JV, Andrade LH, Porto ALM. Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435) [Internet]. Tetrahedron - Asymmetry. 2004 ; 15( 19): 3117-3122.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2004.08.022
Vancouver
Raminelli C, Comasseto JV, Andrade LH, Porto ALM. Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435) [Internet]. Tetrahedron - Asymmetry. 2004 ; 15( 19): 3117-3122.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetasy.2004.08.022
Artigo de periodico
Preparation of chiral organochalcogeno-alpha-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root (2004)
Comasseto, João Valdir; Omori, Álvaro Takeo; Porto, Andre Luiz Meleiro ; Andrade, Leandro Helgueira
Source: Tetrahedron Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, REAGENTES ORGÂNICOS
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ABNT
COMASSETO, João Valdir et al. Preparation of chiral organochalcogeno-alpha-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root. Tetrahedron Letters, v. 45, n. 23, p. 473-476, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2003.11.011. Acesso em: 11 maio 2024.
APA
Comasseto, J. V., Omori, Á. T., Porto, A. L. M., & Andrade, L. H. (2004). Preparation of chiral organochalcogeno-alpha-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root. Tetrahedron Letters, 45( 23), 473-476. doi:10.1016/j.tetlet.2003.11.011
NLM
Comasseto JV, Omori ÁT, Porto ALM, Andrade LH. Preparation of chiral organochalcogeno-alpha-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root [Internet]. Tetrahedron Letters. 2004 ; 45( 23): 473-476.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetlet.2003.11.011
Vancouver
Comasseto JV, Omori ÁT, Porto ALM, Andrade LH. Preparation of chiral organochalcogeno-alpha-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root [Internet]. Tetrahedron Letters. 2004 ; 45( 23): 473-476.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.tetlet.2003.11.011
Artigo de periodico
Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae (2003)
Comasseto, João Valdir; Omori, Álvaro Takeo; Andrade, Leandro Helgueira ; Porto, Andre Luiz Meleiro
Source: Tetrahedron - Asymmetry. Unidade: IQ
Subjects: ASPERGILLUS, ASSIMETRIA (REDUÇÃO), QUÍMICA ORGÂNICA
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ABNT
COMASSETO, João Valdir et al. Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae. Tetrahedron - Asymmetry, v. 14, n. 6, p. 711-715, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0957-4166(03)00096-x. Acesso em: 11 maio 2024.
APA
Comasseto, J. V., Omori, Á. T., Andrade, L. H., & Porto, A. L. M. (2003). Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae. Tetrahedron - Asymmetry, 14( 6), 711-715. doi:10.1016/s0957-4166(03)00096-x
NLM
Comasseto JV, Omori ÁT, Andrade LH, Porto ALM. Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae [Internet]. Tetrahedron - Asymmetry. 2003 ; 14( 6): 711-715.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/s0957-4166(03)00096-x
Vancouver
Comasseto JV, Omori ÁT, Andrade LH, Porto ALM. Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae [Internet]. Tetrahedron - Asymmetry. 2003 ; 14( 6): 711-715.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/s0957-4166(03)00096-x

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