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Artigo de periodico
New reductive addition of hard nucleophiles to 6,7-bis(methyl-sulfanyl)-1,4-dihydro-1,4-methanonaphthalene-5,8-dione (2000)
Di Vitta, Cláudio ; Campos, Ivan Pérsio de Arruda; Farah, João Pedro Simon ; Zukerman-Schpector, Júlio
Fonte: Journal Chemical Society - Perkin Transactions 1. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DI VITTA, Cláudio et al. New reductive addition of hard nucleophiles to 6,7-bis(methyl-sulfanyl)-1,4-dihydro-1,4-methanonaphthalene-5,8-dione. Journal Chemical Society - Perkin Transactions 1, n. 21, p. 3692-3694, 2000Tradução . . Disponível em: https://doi.org/10.1039/b000575o. Acesso em: 29 ago. 2024.
APA
Di Vitta, C., Campos, I. P. de A., Farah, J. P. S., & Zukerman-Schpector, J. (2000). New reductive addition of hard nucleophiles to 6,7-bis(methyl-sulfanyl)-1,4-dihydro-1,4-methanonaphthalene-5,8-dione. Journal Chemical Society - Perkin Transactions 1, ( 21), 3692-3694. doi:10.1039/b000575o
NLM
Di Vitta C, Campos IP de A, Farah JPS, Zukerman-Schpector J. New reductive addition of hard nucleophiles to 6,7-bis(methyl-sulfanyl)-1,4-dihydro-1,4-methanonaphthalene-5,8-dione [Internet]. Journal Chemical Society - Perkin Transactions 1. 2000 ;( 21): 3692-3694.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1039/b000575o
Vancouver
Di Vitta C, Campos IP de A, Farah JPS, Zukerman-Schpector J. New reductive addition of hard nucleophiles to 6,7-bis(methyl-sulfanyl)-1,4-dihydro-1,4-methanonaphthalene-5,8-dione [Internet]. Journal Chemical Society - Perkin Transactions 1. 2000 ;( 21): 3692-3694.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1039/b000575o
Artigo de periodico
New decarboxylative sulfenylation of some phenylsulfonyl arylacetic acids (2000)
Wladislaw, Blanka; Marzorati, Liliana ; Di Vitta, Cláudio ; Claro Júnior, Nélson Ferreira
Fonte: Phosphorus Sulfur and Silicon and the Related Elements. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WLADISLAW, Blanka et al. New decarboxylative sulfenylation of some phenylsulfonyl arylacetic acids. Phosphorus Sulfur and Silicon and the Related Elements, v. 161, p. 1-7, 2000Tradução . . Acesso em: 29 ago. 2024.
APA
Wladislaw, B., Marzorati, L., Di Vitta, C., & Claro Júnior, N. F. (2000). New decarboxylative sulfenylation of some phenylsulfonyl arylacetic acids. Phosphorus Sulfur and Silicon and the Related Elements, 161, 1-7.
NLM
Wladislaw B, Marzorati L, Di Vitta C, Claro Júnior NF. New decarboxylative sulfenylation of some phenylsulfonyl arylacetic acids. Phosphorus Sulfur and Silicon and the Related Elements. 2000 ; 161 1-7.[citado 2024 ago. 29 ]
Vancouver
Wladislaw B, Marzorati L, Di Vitta C, Claro Júnior NF. New decarboxylative sulfenylation of some phenylsulfonyl arylacetic acids. Phosphorus Sulfur and Silicon and the Related Elements. 2000 ; 161 1-7.[citado 2024 ago. 29 ]
Artigo de periodico
Enantioselective diels-alder approach to C-3 oxygenated angucyclinones from (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone (2000)
Carreño, M Carmem; Urbano, Antonio; Di Vitta, Cláudio
Fonte: Chemistry - A European Journal. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARREÑO, M Carmem e URBANO, Antonio e DI VITTA, Cláudio. Enantioselective diels-alder approach to C-3 oxygenated angucyclinones from (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone. Chemistry - A European Journal, v. 6, n. 5, p. 906-913, 2000Tradução . . Acesso em: 29 ago. 2024.
APA
Carreño, M. C., Urbano, A., & Di Vitta, C. (2000). Enantioselective diels-alder approach to C-3 oxygenated angucyclinones from (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone. Chemistry - A European Journal, 6( 5), 906-913.
NLM
Carreño MC, Urbano A, Di Vitta C. Enantioselective diels-alder approach to C-3 oxygenated angucyclinones from (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone. Chemistry - A European Journal. 2000 ; 6( 5): 906-913.[citado 2024 ago. 29 ]
Vancouver
Carreño MC, Urbano A, Di Vitta C. Enantioselective diels-alder approach to C-3 oxygenated angucyclinones from (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone. Chemistry - A European Journal. 2000 ; 6( 5): 906-913.[citado 2024 ago. 29 ]
Artigo de periodico
Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution (2000)
Di Vitta, Cláudio ; Wladislaw, Blanka; Marzorati, Liliana
Fonte: Synthetic Communications. Unidade: IQ
Assuntos: QUÍMICA ORGÂNICA, ENXOFRE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DI VITTA, Cláudio e WLADISLAW, Blanka e MARZORATI, Liliana. Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution. Synthetic Communications, v. 30, n. 18, p. 3413-3422, 2000Tradução . . Acesso em: 29 ago. 2024.
APA
Di Vitta, C., Wladislaw, B., & Marzorati, L. (2000). Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution. Synthetic Communications, 30( 18), 3413-3422.
NLM
Di Vitta C, Wladislaw B, Marzorati L. Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution. Synthetic Communications. 2000 ; 30( 18): 3413-3422.[citado 2024 ago. 29 ]
Vancouver
Di Vitta C, Wladislaw B, Marzorati L. Reactivities of carbonyl-activated angular and vinyl chlorine substituents in chloranyl-cyclopentadiene adduct toward nucleophiles. Synthesis of new 1,4-benzoquinones containing an unusual ortho pattern of substitution. Synthetic Communications. 2000 ; 30( 18): 3413-3422.[citado 2024 ago. 29 ]

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