Fonte: Journal of Organic Chemistry. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
ABNT
CARREÑO, M C e URBANO, Antonio e DI VITTA, Cláudio. Enantioselective Diels-Alder cycloadditions with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone: Efficient kinetic resolution of chiral racemic vinylcyclohexenes. Journal of Organic Chemistry, v. 63, n. 23, p. 8320-8330, 1998Tradução . . Acesso em: 04 out. 2024.APA
Carreño, M. C., Urbano, A., & Di Vitta, C. (1998). Enantioselective Diels-Alder cycloadditions with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone: Efficient kinetic resolution of chiral racemic vinylcyclohexenes. Journal of Organic Chemistry, 63( 23), 8320-8330.NLM
Carreño MC, Urbano A, Di Vitta C. Enantioselective Diels-Alder cycloadditions with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone: Efficient kinetic resolution of chiral racemic vinylcyclohexenes. Journal of Organic Chemistry. 1998 ; 63( 23): 8320-8330.[citado 2024 out. 04 ]Vancouver
Carreño MC, Urbano A, Di Vitta C. Enantioselective Diels-Alder cycloadditions with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone: Efficient kinetic resolution of chiral racemic vinylcyclohexenes. Journal of Organic Chemistry. 1998 ; 63( 23): 8320-8330.[citado 2024 out. 04 ]