ReP USP - Resultado da busca

Artigo de periodico
The nature of the interactions between 'Pt IND.4' cluster and the adsorbates 'ANTIPOT.PONTO'H, 'ANTIPOT.PONTO'OH, and 'H IND.2'O (2008)
Parreira, Renato L. T.; Caramoni, Giovanni F.; Galembeck, Sérgio Emanuel; Huguenin, Fritz
Source: Journal of Physical Chemistry A. Unidade: FFCLRP
Subjects: NANOPARTÍCULAS, QUÍMICA ORGÂNICA
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ABNT
PARREIRA, Renato L. T. et al. The nature of the interactions between 'Pt IND.4' cluster and the adsorbates 'ANTIPOT.PONTO'H, 'ANTIPOT.PONTO'OH, and 'H IND.2'O. Journal of Physical Chemistry A, v. 112, n. 46, p. 11731-11743, 2008Tradução . . Acesso em: 29 jun. 2024.
APA
Parreira, R. L. T., Caramoni, G. F., Galembeck, S. E., & Huguenin, F. (2008). The nature of the interactions between 'Pt IND.4' cluster and the adsorbates 'ANTIPOT.PONTO'H, 'ANTIPOT.PONTO'OH, and 'H IND.2'O. Journal of Physical Chemistry A, 112( 46), 11731-11743.
NLM
Parreira RLT, Caramoni GF, Galembeck SE, Huguenin F. The nature of the interactions between 'Pt IND.4' cluster and the adsorbates 'ANTIPOT.PONTO'H, 'ANTIPOT.PONTO'OH, and 'H IND.2'O. Journal of Physical Chemistry A. 2008 ; 112( 46): 11731-11743.[citado 2024 jun. 29 ]
Vancouver
Parreira RLT, Caramoni GF, Galembeck SE, Huguenin F. The nature of the interactions between 'Pt IND.4' cluster and the adsorbates 'ANTIPOT.PONTO'H, 'ANTIPOT.PONTO'OH, and 'H IND.2'O. Journal of Physical Chemistry A. 2008 ; 112( 46): 11731-11743.[citado 2024 jun. 29 ]
Artigo de periodico
Sub-telomere directed gene expression during initiation of invasive aspergillosis (2008)
McDonagh, Andrew; Fedorova, Natalie D.; Crabtree, Jonathan; Yu, Yan; Kim, Stanley; Chen, Dan; Loss, Omar; Cairns, Timothy; Goldman, Gustavo Henrique; Armstrong-James, Darius; Haynes, Ken; Haas, Hubertus; Schretti, Markus; May, Gregory; Nierman, William C.; Bignell, Elaine
Source: Plos Pathogens. Unidade: FCFRP
Subjects: QUÍMICA ORGÂNICA, ASPERGILLUS, ANTI-HISTAMÍNICOS
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ABNT
MCDONAGH, Andrew et al. Sub-telomere directed gene expression during initiation of invasive aspergillosis. Plos Pathogens, v. 4, n. 9, p. e1000154-1-e1000154-21, 2008Tradução . . Disponível em: https://repositorio.usp.br/directbitstream/d8d32f07-bf55-44ca-9999-1050b34d7985/001705946.pdf. Acesso em: 29 jun. 2024.
APA
McDonagh, A., Fedorova, N. D., Crabtree, J., Yu, Y., Kim, S., Chen, D., et al. (2008). Sub-telomere directed gene expression during initiation of invasive aspergillosis. Plos Pathogens, 4( 9), e1000154-1-e1000154-21. Recuperado de https://repositorio.usp.br/directbitstream/d8d32f07-bf55-44ca-9999-1050b34d7985/001705946.pdf
NLM
McDonagh A, Fedorova ND, Crabtree J, Yu Y, Kim S, Chen D, Loss O, Cairns T, Goldman GH, Armstrong-James D, Haynes K, Haas H, Schretti M, May G, Nierman WC, Bignell E. Sub-telomere directed gene expression during initiation of invasive aspergillosis [Internet]. Plos Pathogens. 2008 ; 4( 9): e1000154-1-e1000154-21.[citado 2024 jun. 29 ] Available from: https://repositorio.usp.br/directbitstream/d8d32f07-bf55-44ca-9999-1050b34d7985/001705946.pdf
Vancouver
McDonagh A, Fedorova ND, Crabtree J, Yu Y, Kim S, Chen D, Loss O, Cairns T, Goldman GH, Armstrong-James D, Haynes K, Haas H, Schretti M, May G, Nierman WC, Bignell E. Sub-telomere directed gene expression during initiation of invasive aspergillosis [Internet]. Plos Pathogens. 2008 ; 4( 9): e1000154-1-e1000154-21.[citado 2024 jun. 29 ] Available from: https://repositorio.usp.br/directbitstream/d8d32f07-bf55-44ca-9999-1050b34d7985/001705946.pdf
Artigo de periodico
Thermosolvatochromism of merocyanine polarity indicators in pure and aqueous solvents: relevance of solvent lipophilicity (2006)
Martins, Clarissa Tavares; Lima, Michelle de Souza; El Seoud, Omar A
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, SOLVENTE
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ABNT
MARTINS, Clarissa Tavares e LIMA, Michelle de Souza e EL SEOUD, Omar A. Thermosolvatochromism of merocyanine polarity indicators in pure and aqueous solvents: relevance of solvent lipophilicity. Journal of Organic Chemistry, v. 71, n. 24, p. 9068-9079, 2006Tradução . . Acesso em: 29 jun. 2024.
APA
Martins, C. T., Lima, M. de S., & El Seoud, O. A. (2006). Thermosolvatochromism of merocyanine polarity indicators in pure and aqueous solvents: relevance of solvent lipophilicity. Journal of Organic Chemistry, 71( 24), 9068-9079.
NLM
Martins CT, Lima M de S, El Seoud OA. Thermosolvatochromism of merocyanine polarity indicators in pure and aqueous solvents: relevance of solvent lipophilicity. Journal of Organic Chemistry. 2006 ; 71( 24): 9068-9079.[citado 2024 jun. 29 ]
Vancouver
Martins CT, Lima M de S, El Seoud OA. Thermosolvatochromism of merocyanine polarity indicators in pure and aqueous solvents: relevance of solvent lipophilicity. Journal of Organic Chemistry. 2006 ; 71( 24): 9068-9079.[citado 2024 jun. 29 ]
Artigo de periodico
A computational study of [2.2] cyclophanes (2005)
Caramori, Giovanni F.; Galembeck, Sérgio Emanuel; Laali, Kenneth K.
Source: Journal of Organic Chemistry. Unidade: FFCLRP
Subjects: ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA), VARIAÇÕES ESTRUTURAIS, QUÍMICA ORGÂNICA
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ABNT
CARAMORI, Giovanni F. e GALEMBECK, Sérgio Emanuel e LAALI, Kenneth K. A computational study of [2.2] cyclophanes. Journal of Organic Chemistry, v. 70, n. 8, p. 3242-3250, 2005Tradução . . Acesso em: 29 jun. 2024.
APA
Caramori, G. F., Galembeck, S. E., & Laali, K. K. (2005). A computational study of [2.2] cyclophanes. Journal of Organic Chemistry, 70( 8), 3242-3250.
NLM
Caramori GF, Galembeck SE, Laali KK. A computational study of [2.2] cyclophanes. Journal of Organic Chemistry. 2005 ; 70( 8): 3242-3250.[citado 2024 jun. 29 ]
Vancouver
Caramori GF, Galembeck SE, Laali KK. A computational study of [2.2] cyclophanes. Journal of Organic Chemistry. 2005 ; 70( 8): 3242-3250.[citado 2024 jun. 29 ]
Artigo de periodico
Unexpected synthesis of conformationally restricted analogues of gamma-amino butyric acid (GABA): Mechanism elucidation by electrospray ionization mass spectrometry (2005)
Ferraz, Helena Maria Carvalho; Pereira, Fernando Luiz Cardoso; Gonçalo, Erika Rocha da Silva; Santos, Leonardo Silva; Eberlin, Marcos Nogueira
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, REAÇÕES ORGÂNICAS
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ABNT
FERRAZ, Helena Maria Carvalho et al. Unexpected synthesis of conformationally restricted analogues of gamma-amino butyric acid (GABA): Mechanism elucidation by electrospray ionization mass spectrometry. Journal of Organic Chemistry, v. 70, n. 1, p. 110-114, 2005Tradução . . Acesso em: 29 jun. 2024.
APA
Ferraz, H. M. C., Pereira, F. L. C., Gonçalo, E. R. da S., Santos, L. S., & Eberlin, M. N. (2005). Unexpected synthesis of conformationally restricted analogues of gamma-amino butyric acid (GABA): Mechanism elucidation by electrospray ionization mass spectrometry. Journal of Organic Chemistry, 70( 1), 110-114.
NLM
Ferraz HMC, Pereira FLC, Gonçalo ER da S, Santos LS, Eberlin MN. Unexpected synthesis of conformationally restricted analogues of gamma-amino butyric acid (GABA): Mechanism elucidation by electrospray ionization mass spectrometry. Journal of Organic Chemistry. 2005 ; 70( 1): 110-114.[citado 2024 jun. 29 ]
Vancouver
Ferraz HMC, Pereira FLC, Gonçalo ER da S, Santos LS, Eberlin MN. Unexpected synthesis of conformationally restricted analogues of gamma-amino butyric acid (GABA): Mechanism elucidation by electrospray ionization mass spectrometry. Journal of Organic Chemistry. 2005 ; 70( 1): 110-114.[citado 2024 jun. 29 ]
Artigo de periodico
Effect of alkyl group size on the mechanism of acid hydrolyses of benzaldehyde acetals (2003)
Belarmino, Alexanders T. N.; Froehner, Sandro; Zanette, Dino; Farah, João Pedro Simon ; Bunton, Clifford A.; Romsted, Laurence S.
Source: Journal of Organic Chemistry. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, HIDRÓLISE
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ABNT
BELARMINO, Alexanders T. N. et al. Effect of alkyl group size on the mechanism of acid hydrolyses of benzaldehyde acetals. Journal of Organic Chemistry, v. 68, n. 3, p. 706-717, 2003Tradução . . Acesso em: 29 jun. 2024.
APA
Belarmino, A. T. N., Froehner, S., Zanette, D., Farah, J. P. S., Bunton, C. A., & Romsted, L. S. (2003). Effect of alkyl group size on the mechanism of acid hydrolyses of benzaldehyde acetals. Journal of Organic Chemistry, 68( 3), 706-717.
NLM
Belarmino ATN, Froehner S, Zanette D, Farah JPS, Bunton CA, Romsted LS. Effect of alkyl group size on the mechanism of acid hydrolyses of benzaldehyde acetals. Journal of Organic Chemistry. 2003 ; 68( 3): 706-717.[citado 2024 jun. 29 ]
Vancouver
Belarmino ATN, Froehner S, Zanette D, Farah JPS, Bunton CA, Romsted LS. Effect of alkyl group size on the mechanism of acid hydrolyses of benzaldehyde acetals. Journal of Organic Chemistry. 2003 ; 68( 3): 706-717.[citado 2024 jun. 29 ]
Artigo de periodico
Efficient entry into medium-ring keto-lactones. The ruthenium tetraoxide-promoted oxidative cleavage of beta-hydroxyethers (2003)
Ferraz, Helena Maria Carvalho; Longo Junior, Luiz Sidney
Source: Organic Letters. Unidade: IQ
Subjects: HIDROCARBONOS, QUÍMICA ORGÂNICA
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ABNT
FERRAZ, Helena Maria Carvalho e LONGO JUNIOR, Luiz Sidney. Efficient entry into medium-ring keto-lactones. The ruthenium tetraoxide-promoted oxidative cleavage of beta-hydroxyethers. Organic Letters, v. 5, n. 8, p. 1337-1339, 2003Tradução . . Acesso em: 29 jun. 2024.
APA
Ferraz, H. M. C., & Longo Junior, L. S. (2003). Efficient entry into medium-ring keto-lactones. The ruthenium tetraoxide-promoted oxidative cleavage of beta-hydroxyethers. Organic Letters, 5( 8), 1337-1339.
NLM
Ferraz HMC, Longo Junior LS. Efficient entry into medium-ring keto-lactones. The ruthenium tetraoxide-promoted oxidative cleavage of beta-hydroxyethers. Organic Letters. 2003 ; 5( 8): 1337-1339.[citado 2024 jun. 29 ]
Vancouver
Ferraz HMC, Longo Junior LS. Efficient entry into medium-ring keto-lactones. The ruthenium tetraoxide-promoted oxidative cleavage of beta-hydroxyethers. Organic Letters. 2003 ; 5( 8): 1337-1339.[citado 2024 jun. 29 ]
Artigo de periodico
Genotoxic action of the sesquiterpene lactone centratherin on mammalian cells in vitro and in vivo (2001)
Burim, Regislaine Valéria; Canalle, Renata; Lopes, João Luís Callegari; Vichnewski, Walter; Takahashi, Catarina Satie
Source: Teratogenesis, Carcinogenesis and Mutagenesis. Unidades: FCFRP, FFCLRP
Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA, MUTAÇÃO GENÉTICA, LINFÓCITOS
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ABNT
BURIM, Regislaine Valéria et al. Genotoxic action of the sesquiterpene lactone centratherin on mammalian cells in vitro and in vivo. Teratogenesis, Carcinogenesis and Mutagenesis, v. 21, n. 6, p. 383-393, 2001Tradução . . Disponível em: https://doi.org/10.1002/tcm.1026. Acesso em: 29 jun. 2024.
APA
Burim, R. V., Canalle, R., Lopes, J. L. C., Vichnewski, W., & Takahashi, C. S. (2001). Genotoxic action of the sesquiterpene lactone centratherin on mammalian cells in vitro and in vivo. Teratogenesis, Carcinogenesis and Mutagenesis, 21( 6), 383-393. doi:10.1002/tcm.1026
NLM
Burim RV, Canalle R, Lopes JLC, Vichnewski W, Takahashi CS. Genotoxic action of the sesquiterpene lactone centratherin on mammalian cells in vitro and in vivo [Internet]. Teratogenesis, Carcinogenesis and Mutagenesis. 2001 ; 21( 6): 383-393.[citado 2024 jun. 29 ] Available from: https://doi.org/10.1002/tcm.1026
Vancouver
Burim RV, Canalle R, Lopes JLC, Vichnewski W, Takahashi CS. Genotoxic action of the sesquiterpene lactone centratherin on mammalian cells in vitro and in vivo [Internet]. Teratogenesis, Carcinogenesis and Mutagenesis. 2001 ; 21( 6): 383-393.[citado 2024 jun. 29 ] Available from: https://doi.org/10.1002/tcm.1026
Artigo de periodico
Calculated and experimental NMR chemical shifts of p-menthane-3,9-diols: a combination of molecular dynamics and quantum mechanics to determine the structure and the solvent effects (2001)
Casanovas, Jordi; Namba, Adriana Mieco; León, Salvador; Aquino, Gilberto Lucio Benedito de; Silva, Gil Valdo José da; Alemán, Carlos
Source: Journal of Organic Chemistry. Unidade: FFCLRP
Assunto: QUÍMICA ORGÂNICA
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ABNT
CASANOVAS, Jordi et al. Calculated and experimental NMR chemical shifts of p-menthane-3,9-diols: a combination of molecular dynamics and quantum mechanics to determine the structure and the solvent effects. Journal of Organic Chemistry, v. 66, p. 3775-3782, 2001Tradução . . Acesso em: 29 jun. 2024.
APA
Casanovas, J., Namba, A. M., León, S., Aquino, G. L. B. de, Silva, G. V. J. da, & Alemán, C. (2001). Calculated and experimental NMR chemical shifts of p-menthane-3,9-diols: a combination of molecular dynamics and quantum mechanics to determine the structure and the solvent effects. Journal of Organic Chemistry, 66, 3775-3782.
NLM
Casanovas J, Namba AM, León S, Aquino GLB de, Silva GVJ da, Alemán C. Calculated and experimental NMR chemical shifts of p-menthane-3,9-diols: a combination of molecular dynamics and quantum mechanics to determine the structure and the solvent effects. Journal of Organic Chemistry. 2001 ; 66 3775-3782.[citado 2024 jun. 29 ]
Vancouver
Casanovas J, Namba AM, León S, Aquino GLB de, Silva GVJ da, Alemán C. Calculated and experimental NMR chemical shifts of p-menthane-3,9-diols: a combination of molecular dynamics and quantum mechanics to determine the structure and the solvent effects. Journal of Organic Chemistry. 2001 ; 66 3775-3782.[citado 2024 jun. 29 ]
Artigo de periodico
The oxidation of indole derivatives catalyzed by horseradish peroxidase is highly chemiluminescent (2001)
Ximenes, Valdecir Farias; Campa, Ana ; Catalani, Luiz Henrique
Source: Archives of Biochemistry and Biophysics. Unidades: FCF, IQ
Assunto: QUÍMICA ORGÂNICA
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ABNT
XIMENES, Valdecir Farias e CAMPA, Ana e CATALANI, Luiz Henrique. The oxidation of indole derivatives catalyzed by horseradish peroxidase is highly chemiluminescent. Archives of Biochemistry and Biophysics, v. 387, n. 2, p. 173-179, 2001Tradução . . Disponível em: http://www.idealibrary.com/links/doi/10.1006/abbi.2000.2228/pdf. Acesso em: 29 jun. 2024.
APA
Ximenes, V. F., Campa, A., & Catalani, L. H. (2001). The oxidation of indole derivatives catalyzed by horseradish peroxidase is highly chemiluminescent. Archives of Biochemistry and Biophysics, 387( 2), 173-179. Recuperado de http://www.idealibrary.com/links/doi/10.1006/abbi.2000.2228/pdf
NLM
Ximenes VF, Campa A, Catalani LH. The oxidation of indole derivatives catalyzed by horseradish peroxidase is highly chemiluminescent [Internet]. Archives of Biochemistry and Biophysics. 2001 ; 387( 2): 173-179.[citado 2024 jun. 29 ] Available from: http://www.idealibrary.com/links/doi/10.1006/abbi.2000.2228/pdf
Vancouver
Ximenes VF, Campa A, Catalani LH. The oxidation of indole derivatives catalyzed by horseradish peroxidase is highly chemiluminescent [Internet]. Archives of Biochemistry and Biophysics. 2001 ; 387( 2): 173-179.[citado 2024 jun. 29 ] Available from: http://www.idealibrary.com/links/doi/10.1006/abbi.2000.2228/pdf
Artigo de periodico
Persistent oxidation dications from twisted fluoranthenes, Benzo[k]fluoranthene and dimethyldibenzo[j.l]fluoranthene: charge delocalization mode, tropicity, and formation of novel 8,8'-bifluoanthenyls. An NMR and theoretical study (2001)
Laali, Kenneth K.; Okazaki, Takao; Galembeck, Sérgio Emanuel; Siegel, Jay S.
Source: Journal of Organic Chemistry. Unidade: FFCLRP
Assunto: QUÍMICA ORGÂNICA
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ABNT
LAALI, Kenneth K. et al. Persistent oxidation dications from twisted fluoranthenes, Benzo[k]fluoranthene and dimethyldibenzo[j.l]fluoranthene: charge delocalization mode, tropicity, and formation of novel 8,8'-bifluoanthenyls. An NMR and theoretical study. Journal of Organic Chemistry, v. 66, p. 8701-8708, 2001Tradução . . Acesso em: 29 jun. 2024.
APA
Laali, K. K., Okazaki, T., Galembeck, S. E., & Siegel, J. S. (2001). Persistent oxidation dications from twisted fluoranthenes, Benzo[k]fluoranthene and dimethyldibenzo[j.l]fluoranthene: charge delocalization mode, tropicity, and formation of novel 8,8'-bifluoanthenyls. An NMR and theoretical study. Journal of Organic Chemistry, 66, 8701-8708.
NLM
Laali KK, Okazaki T, Galembeck SE, Siegel JS. Persistent oxidation dications from twisted fluoranthenes, Benzo[k]fluoranthene and dimethyldibenzo[j.l]fluoranthene: charge delocalization mode, tropicity, and formation of novel 8,8'-bifluoanthenyls. An NMR and theoretical study. Journal of Organic Chemistry. 2001 ; 66 8701-8708.[citado 2024 jun. 29 ]
Vancouver
Laali KK, Okazaki T, Galembeck SE, Siegel JS. Persistent oxidation dications from twisted fluoranthenes, Benzo[k]fluoranthene and dimethyldibenzo[j.l]fluoranthene: charge delocalization mode, tropicity, and formation of novel 8,8'-bifluoanthenyls. An NMR and theoretical study. Journal of Organic Chemistry. 2001 ; 66 8701-8708.[citado 2024 jun. 29 ]
Artigo de periodico
Protective effect of lycopene on lipid peroxidation and oxidative DNA damage in cell culture (2000)
Matos, Humberto R; Di Mascio, Paolo ; Medeiros, Marisa Helena Gennari de
Source: Archives of Biochemistry and Biophysics. Unidade: IQ
Subjects: BIOQUÍMICA, QUÍMICA ORGÂNICA
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ABNT
MATOS, Humberto R e DI MASCIO, Paolo e MEDEIROS, Marisa Helena Gennari de. Protective effect of lycopene on lipid peroxidation and oxidative DNA damage in cell culture. Archives of Biochemistry and Biophysics, v. 383, n. 1, p. 56-59, 2000Tradução . . Acesso em: 29 jun. 2024.
APA
Matos, H. R., Di Mascio, P., & Medeiros, M. H. G. de. (2000). Protective effect of lycopene on lipid peroxidation and oxidative DNA damage in cell culture. Archives of Biochemistry and Biophysics, 383( 1), 56-59.
NLM
Matos HR, Di Mascio P, Medeiros MHG de. Protective effect of lycopene on lipid peroxidation and oxidative DNA damage in cell culture. Archives of Biochemistry and Biophysics. 2000 ; 383( 1): 56-59.[citado 2024 jun. 29 ]
Vancouver
Matos HR, Di Mascio P, Medeiros MHG de. Protective effect of lycopene on lipid peroxidation and oxidative DNA damage in cell culture. Archives of Biochemistry and Biophysics. 2000 ; 383( 1): 56-59.[citado 2024 jun. 29 ]
Artigo de periodico
Hydrozirconation of stannylacetylenes: synthesis and reactions of ketene stannyl (Telluro) acetals (2000)
Dabdoub, Miguel Joaquim; Baroni, Adriano Cesar de Morais
Source: Journal of Organic Chemistry. Unidade: FFCLRP
Assunto: QUÍMICA ORGÂNICA
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ABNT
DABDOUB, Miguel Joaquim e BARONI, Adriano Cesar de Morais. Hydrozirconation of stannylacetylenes: synthesis and reactions of ketene stannyl (Telluro) acetals. Journal of Organic Chemistry, v. 65, n. 1, p. 54-60, 2000Tradução . . Acesso em: 29 jun. 2024.
APA
Dabdoub, M. J., & Baroni, A. C. de M. (2000). Hydrozirconation of stannylacetylenes: synthesis and reactions of ketene stannyl (Telluro) acetals. Journal of Organic Chemistry, 65( 1), 54-60.
NLM
Dabdoub MJ, Baroni AC de M. Hydrozirconation of stannylacetylenes: synthesis and reactions of ketene stannyl (Telluro) acetals. Journal of Organic Chemistry. 2000 ; 65( 1): 54-60.[citado 2024 jun. 29 ]
Vancouver
Dabdoub MJ, Baroni AC de M. Hydrozirconation of stannylacetylenes: synthesis and reactions of ketene stannyl (Telluro) acetals. Journal of Organic Chemistry. 2000 ; 65( 1): 54-60.[citado 2024 jun. 29 ]
Artigo de periodico
Hydrozirconation of lithium alkynylselenolate anions: generation and reactions of 'alfa'-zirconated vinyl selenide intermediates (2000)
Dabdoub, Miguel Joaquim; Begnini, Mauro Luiz; Guerrero, Palimécio G.; Baroni, Adriano Cesar de Morais
Source: Journal of Organic Chemistry. Unidade: FFCLRP
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DABDOUB, Miguel Joaquim et al. Hydrozirconation of lithium alkynylselenolate anions: generation and reactions of 'alfa'-zirconated vinyl selenide intermediates. Journal of Organic Chemistry, v. 65, n. 1, p. 61-67, 2000Tradução . . Acesso em: 29 jun. 2024.
APA
Dabdoub, M. J., Begnini, M. L., Guerrero, P. G., & Baroni, A. C. de M. (2000). Hydrozirconation of lithium alkynylselenolate anions: generation and reactions of 'alfa'-zirconated vinyl selenide intermediates. Journal of Organic Chemistry, 65( 1), 61-67.
NLM
Dabdoub MJ, Begnini ML, Guerrero PG, Baroni AC de M. Hydrozirconation of lithium alkynylselenolate anions: generation and reactions of 'alfa'-zirconated vinyl selenide intermediates. Journal of Organic Chemistry. 2000 ; 65( 1): 61-67.[citado 2024 jun. 29 ]
Vancouver
Dabdoub MJ, Begnini ML, Guerrero PG, Baroni AC de M. Hydrozirconation of lithium alkynylselenolate anions: generation and reactions of 'alfa'-zirconated vinyl selenide intermediates. Journal of Organic Chemistry. 2000 ; 65( 1): 61-67.[citado 2024 jun. 29 ]
Artigo de periodico
Conformational preferences of 2,3,3a,8a-Tetrahydrofuro[2,3-b]benzofuran: the chemical Modifications drive the pseudoratational preferences (1999)
Alemán, Carlos; Donate, Paulo Marcos; Silva, Rosangela da; Silva, Gil Valdo José da
Source: Journal of Organic Chemistry. Unidade: FFCLRP
Assunto: QUÍMICA ORGÂNICA
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ABNT
ALEMÁN, Carlos et al. Conformational preferences of 2,3,3a,8a-Tetrahydrofuro[2,3-b]benzofuran: the chemical Modifications drive the pseudoratational preferences. Journal of Organic Chemistry, v. 65, p. 5712-5714, 1999Tradução . . Acesso em: 29 jun. 2024.
APA
Alemán, C., Donate, P. M., Silva, R. da, & Silva, G. V. J. da. (1999). Conformational preferences of 2,3,3a,8a-Tetrahydrofuro[2,3-b]benzofuran: the chemical Modifications drive the pseudoratational preferences. Journal of Organic Chemistry, 65, 5712-5714.
NLM
Alemán C, Donate PM, Silva R da, Silva GVJ da. Conformational preferences of 2,3,3a,8a-Tetrahydrofuro[2,3-b]benzofuran: the chemical Modifications drive the pseudoratational preferences. Journal of Organic Chemistry. 1999 ; 65 5712-5714.[citado 2024 jun. 29 ]
Vancouver
Alemán C, Donate PM, Silva R da, Silva GVJ da. Conformational preferences of 2,3,3a,8a-Tetrahydrofuro[2,3-b]benzofuran: the chemical Modifications drive the pseudoratational preferences. Journal of Organic Chemistry. 1999 ; 65 5712-5714.[citado 2024 jun. 29 ]

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