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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: 02 nov. 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 nov. 02 ]
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 nov. 02 ]
Artigo de periodico
Electrospray mass spectrometric and DFT study of substituent effects in 'Ag POT.+' complexation to polycyclic aromatic hydrocarbons (PAHs) (2005)
Laali, Kenneth K.; Hupertz, Scott; Temu, Alice G.; Galembeck, Sérgio Emanuel
Source: Organic and Biomolecular Chemistry. Unidade: FFCLRP
Assunto: ELETROQUÍMICA
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ABNT
LAALI, Kenneth K. et al. Electrospray mass spectrometric and DFT study of substituent effects in 'Ag POT.+' complexation to polycyclic aromatic hydrocarbons (PAHs). Organic and Biomolecular Chemistry, v. 3, p. 2319-2326, 2005Tradução . . Disponível em: https://doi.org/10.1039/b503084f. Acesso em: 02 nov. 2024.
APA
Laali, K. K., Hupertz, S., Temu, A. G., & Galembeck, S. E. (2005). Electrospray mass spectrometric and DFT study of substituent effects in 'Ag POT.+' complexation to polycyclic aromatic hydrocarbons (PAHs). Organic and Biomolecular Chemistry, 3, 2319-2326. doi:10.1039/b503084f
NLM
Laali KK, Hupertz S, Temu AG, Galembeck SE. Electrospray mass spectrometric and DFT study of substituent effects in 'Ag POT.+' complexation to polycyclic aromatic hydrocarbons (PAHs) [Internet]. Organic and Biomolecular Chemistry. 2005 ; 3 2319-2326.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1039/b503084f
Vancouver
Laali KK, Hupertz S, Temu AG, Galembeck SE. Electrospray mass spectrometric and DFT study of substituent effects in 'Ag POT.+' complexation to polycyclic aromatic hydrocarbons (PAHs) [Internet]. Organic and Biomolecular Chemistry. 2005 ; 3 2319-2326.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1039/b503084f
Trabalho de evento-resumo
Computational study of cyclophates (2003)
Caramori, Giovanni Finoto; Galembeck, Sérgio Emanuel; Laali, Kenneth K.
Source: Abstracts. Conference titles: Conferência Latinoamericana de Físico-Química Orgânica. Unidade: FFCLRP
Assunto: FÍSICO-QUÍMICA
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ABNT
CARAMORI, Giovanni Finoto e GALEMBECK, Sérgio Emanuel e LAALI, Kenneth K. Computational study of cyclophates. 2003, Anais.. Florianópolis: Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, 2003. . Acesso em: 02 nov. 2024.
APA
Caramori, G. F., Galembeck, S. E., & Laali, K. K. (2003). Computational study of cyclophates. In Abstracts. Florianópolis: Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo.
NLM
Caramori GF, Galembeck SE, Laali KK. Computational study of cyclophates. Abstracts. 2003 ;[citado 2024 nov. 02 ]
Vancouver
Caramori GF, Galembeck SE, Laali KK. Computational study of cyclophates. Abstracts. 2003 ;[citado 2024 nov. 02 ]
Artigo de periodico
Novel examples of three-dimensional aromaticity: 1,3-Dehydro-silaadamantane dications. A theoretical (DFT, GIAO NMR, NICS) study (2002)
Okazaki, Takao; Laali, Kenneth K.; Galembeck, Sérgio Emanuel
Source: Journal of Organic Chemistry. Unidade: FFCLRP
Assunto: QUÍMICA INORGÂNICA
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ABNT
OKAZAKI, Takao e LAALI, Kenneth K. e GALEMBECK, Sérgio Emanuel. Novel examples of three-dimensional aromaticity: 1,3-Dehydro-silaadamantane dications. A theoretical (DFT, GIAO NMR, NICS) study. Journal of Organic Chemistry, v. 67, n. 25, p. 8721-8725, 2002Tradução . . Acesso em: 02 nov. 2024.
APA
Okazaki, T., Laali, K. K., & Galembeck, S. E. (2002). Novel examples of three-dimensional aromaticity: 1,3-Dehydro-silaadamantane dications. A theoretical (DFT, GIAO NMR, NICS) study. Journal of Organic Chemistry, 67( 25), 8721-8725.
NLM
Okazaki T, Laali KK, Galembeck SE. Novel examples of three-dimensional aromaticity: 1,3-Dehydro-silaadamantane dications. A theoretical (DFT, GIAO NMR, NICS) study. Journal of Organic Chemistry. 2002 ; 67( 25): 8721-8725.[citado 2024 nov. 02 ]
Vancouver
Okazaki T, Laali KK, Galembeck SE. Novel examples of three-dimensional aromaticity: 1,3-Dehydro-silaadamantane dications. A theoretical (DFT, GIAO NMR, NICS) study. Journal of Organic Chemistry. 2002 ; 67( 25): 8721-8725.[citado 2024 nov. 02 ]
Artigo de periodico
Stable ion and electrophilic chemistry of fluoranthene-PAHS (2002)
Laali, Kenneth K.; Okazaki, Takao; Galembeck, Sérgio Emanuel
Source: Journal of Chemical Society - Perkin Transactions, 2. Unidade: FFCLRP
Assunto: FÍSICO-QUÍMICA
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ABNT
LAALI, Kenneth K. e OKAZAKI, Takao e GALEMBECK, Sérgio Emanuel. Stable ion and electrophilic chemistry of fluoranthene-PAHS. Journal of Chemical Society - Perkin Transactions, 2, n. 3, p. 621-629, 2002Tradução . . Disponível em: http://www.rsc.org/suppdata/p2/b1/b108025n/. Acesso em: 02 nov. 2024.
APA
Laali, K. K., Okazaki, T., & Galembeck, S. E. (2002). Stable ion and electrophilic chemistry of fluoranthene-PAHS. Journal of Chemical Society - Perkin Transactions, 2, ( 3), 621-629. Recuperado de http://www.rsc.org/suppdata/p2/b1/b108025n/
NLM
Laali KK, Okazaki T, Galembeck SE. Stable ion and electrophilic chemistry of fluoranthene-PAHS [Internet]. Journal of Chemical Society - Perkin Transactions, 2. 2002 ;( 3): 621-629.[citado 2024 nov. 02 ] Available from: http://www.rsc.org/suppdata/p2/b1/b108025n/
Vancouver
Laali KK, Okazaki T, Galembeck SE. Stable ion and electrophilic chemistry of fluoranthene-PAHS [Internet]. Journal of Chemical Society - Perkin Transactions, 2. 2002 ;( 3): 621-629.[citado 2024 nov. 02 ] Available from: http://www.rsc.org/suppdata/p2/b1/b108025n/
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: 02 nov. 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 nov. 02 ]
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 nov. 02 ]
Artigo de periodico
Substituent effects and charge delocalization mode in chrysenium, benzo[c]phenanthrenium, and benzo[g]chrysenium cations: a stable ion and electrophilic substitution study (2001)
Laali, Kenneth K.; Okazaki, Takao; Kumar, Subodh; Galembeck, Sérgio Emanuel
Source: Journal of Organic Chemistry. Unidade: FFCLRP
Assunto: QUÍMICA ORGÂNICA
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ABNT
LAALI, Kenneth K. et al. Substituent effects and charge delocalization mode in chrysenium, benzo[c]phenanthrenium, and benzo[g]chrysenium cations: a stable ion and electrophilic substitution study. Journal of Organic Chemistry, v. 66, p. 780-788, 2001Tradução . . Acesso em: 02 nov. 2024.
APA
Laali, K. K., Okazaki, T., Kumar, S., & Galembeck, S. E. (2001). Substituent effects and charge delocalization mode in chrysenium, benzo[c]phenanthrenium, and benzo[g]chrysenium cations: a stable ion and electrophilic substitution study. Journal of Organic Chemistry, 66, 780-788.
NLM
Laali KK, Okazaki T, Kumar S, Galembeck SE. Substituent effects and charge delocalization mode in chrysenium, benzo[c]phenanthrenium, and benzo[g]chrysenium cations: a stable ion and electrophilic substitution study. Journal of Organic Chemistry. 2001 ; 66 780-788.[citado 2024 nov. 02 ]
Vancouver
Laali KK, Okazaki T, Kumar S, Galembeck SE. Substituent effects and charge delocalization mode in chrysenium, benzo[c]phenanthrenium, and benzo[g]chrysenium cations: a stable ion and electrophilic substitution study. Journal of Organic Chemistry. 2001 ; 66 780-788.[citado 2024 nov. 02 ]
Artigo de periodico
Stabel ion study of protonated cyclopenta[a]phenanthrenes: structure-reactivity relationships and charge delocalization in the carbocations (2000)
Laali, Kenneth K.; Hollenstein, Sandro; Galembeck, Sérgio Emanuel; Coombs, Maurice M.
Source: Journal of the Chemical Society. Unidade: FFCLRP
Assunto: FÍSICO-QUÍMICA
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ABNT
LAALI, Kenneth K. et al. Stabel ion study of protonated cyclopenta[a]phenanthrenes: structure-reactivity relationships and charge delocalization in the carbocations. Journal of the Chemical Society, p. 211-220, 2000Tradução . . Acesso em: 02 nov. 2024.
APA
Laali, K. K., Hollenstein, S., Galembeck, S. E., & Coombs, M. M. (2000). Stabel ion study of protonated cyclopenta[a]phenanthrenes: structure-reactivity relationships and charge delocalization in the carbocations. Journal of the Chemical Society, 211-220.
NLM
Laali KK, Hollenstein S, Galembeck SE, Coombs MM. Stabel ion study of protonated cyclopenta[a]phenanthrenes: structure-reactivity relationships and charge delocalization in the carbocations. Journal of the Chemical Society. 2000 ; 211-220.[citado 2024 nov. 02 ]
Vancouver
Laali KK, Hollenstein S, Galembeck SE, Coombs MM. Stabel ion study of protonated cyclopenta[a]phenanthrenes: structure-reactivity relationships and charge delocalization in the carbocations. Journal of the Chemical Society. 2000 ; 211-220.[citado 2024 nov. 02 ]
Artigo de periodico
Superacid protonation of dihydrocyclobuta[e]pyrene and its 'C IND. 60'-o-quinodimethane adduct. An NMR, ab initio/GIAO and AMI/PM3 study (1999)
Laali, Kenneth K.; Hollenstein, Sandro; Galembeck, Sergio Emanuel; Nakamura, Yosuke; Nishimura, Jun
Source: Journal of the Royal Society of Chemistry. Perkin Tansactions 2. Unidade: FFCLRP
Assunto: QUÍMICA
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ABNT
LAALI, Kenneth K. et al. Superacid protonation of dihydrocyclobuta[e]pyrene and its 'C IND. 60'-o-quinodimethane adduct. An NMR, ab initio/GIAO and AMI/PM3 study. Journal of the Royal Society of Chemistry. Perkin Tansactions 2, n. 10, p. 2129-2132, 1999Tradução . . Acesso em: 02 nov. 2024.
APA
Laali, K. K., Hollenstein, S., Galembeck, S. E., Nakamura, Y., & Nishimura, J. (1999). Superacid protonation of dihydrocyclobuta[e]pyrene and its 'C IND. 60'-o-quinodimethane adduct. An NMR, ab initio/GIAO and AMI/PM3 study. Journal of the Royal Society of Chemistry. Perkin Tansactions 2, ( 10), 2129-2132.
NLM
Laali KK, Hollenstein S, Galembeck SE, Nakamura Y, Nishimura J. Superacid protonation of dihydrocyclobuta[e]pyrene and its 'C IND. 60'-o-quinodimethane adduct. An NMR, ab initio/GIAO and AMI/PM3 study. Journal of the Royal Society of Chemistry. Perkin Tansactions 2. 1999 ;( 10): 2129-2132.[citado 2024 nov. 02 ]
Vancouver
Laali KK, Hollenstein S, Galembeck SE, Nakamura Y, Nishimura J. Superacid protonation of dihydrocyclobuta[e]pyrene and its 'C IND. 60'-o-quinodimethane adduct. An NMR, ab initio/GIAO and AMI/PM3 study. Journal of the Royal Society of Chemistry. Perkin Tansactions 2. 1999 ;( 10): 2129-2132.[citado 2024 nov. 02 ]

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