91855-97-9Relevant academic research and scientific papers
1,4-Naphthoquinones, VII: C-Methylation of 1,4-Naphthoquinones
Wurm, Gotthard,Geres, Uwe
, p. 606 - 609 (1984)
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.
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
Enantioselective Total Synthesis of (?)-Spiroxins A, C, and D
Chen, Chong-Chong,Hu, Xiangdong,Shu, Xin,Yang, Jiayi,Yu, Tao
supporting information, p. 18514 - 18518 (2021/07/20)
Spiroxins A, C, and D are metabolites that have been identified in the marine fungal strain LL-37H248. Their unique polycyclic structures and intriguing biological activities make them attractive targets for the synthetic community. Based on a scalable en
