Di Vitta, Cláudio 
; Wladislaw, Blanka; Marzorati, Liliana
Source: Synthetic Communications. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, ENXOFRE
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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 ]
