70871-48-6Relevant academic research and scientific papers
Molecular anchors - Mimicking metabolic processes in thiol analysis
Smith, Robert B.,Canton, Claire,Lawrence, Nathan S.,Livingstone, Callum,Davis, James
, p. 1718 - 1724 (2006)
The interaction between various novel naphthoquinones and glutathione was explored using a variety of electrochemical techniques. An adamantane derivatised quinone was found to adsorb strongly to carbon surfaces providing a robust film possessing a distin
Synthesis, biological evaluation, and correlation of cytotoxicity versus redox potential of 1,4-naphthoquinone derivatives
Shen, Chien-Chang,Afraj, Shakil N.,Hung, Chia-Cheng,Barve, Balaji D.,Kuo, Li-Ming Yang,Lin, Zhi-Hu,Ho, Hisu-O.,Kuo, Yao-Haur
supporting information, (2021/04/12)
A series of 1,4-naphthoquinone derivatives of lawsone (1), 6-hydroxy-1,4-naphthoquinone (2), and juglone (3) were synthesized by alkylation, acylation, and sulfonylation reactions. The yields of lawsone derivatives 1a-1k (type A), 6-hydroxy-1,4-naphthoqui
1,4-Naphthoquinones, VII: C-Methylation of 1,4-Naphthoquinones
Wurm, Gotthard,Geres, Uwe
, p. 606 - 609 (2007/10/02)
The action of Fenton's reagent on dimethyl sulfoxide results in carbon methylation of the quinoid system of 1,4-naphthoquinones by .CH3 under particularly mild conditions.The results depend on the substitution pattern at positions 2 and 3 and on the suitable protection of the OH group at position 5.
Photochemical Reactivity of α-Sulfonyloxy Enones: An Easy Method for Arylation of 1,2-Diketones
Feigenbaum, Alexandre,Pete, Jean-Pierre,Scholler, Denise
, p. 2355 - 2360 (2007/10/02)
3-Aryl-1,2-cyclohexanediones 4 are prepared conveniently by photolysis of the corresponding 2-((arylsulfonyl)oxy)cyclohex-2-enones 1.The reaction was shown to occur from a triplet excited state.A biphotonic process involving the normal photo-Fries product 14 as an intermediate was ruled out by preparing and irradiating this compound.The difference of reactivity between 1 and 2-((arylsulfonyl)amido)cyclohexenones is discussed.
