80931-34-6Relevant articles and documents
Concise synthesis of heterocycle-fused naphthoquinones by employing sonogashira coupling and tandem addition-elimination/intramolecular cyclization
Ueda, Kazunori,Yamashita, Mitsuaki,Sakaguchi, Koichi,Tokuda, Harukuni,Iida, Akira
, p. 648 - 654 (2013/07/11)
A concise method for the synthesis of heterocycle-fused naphthoquinones such as naphtho[2,3-b]-furan-4,9-dione, 1H-benz[f]indole-4,9-dione, and naphtho[2,3-b]thiophene-4,9-dione was developed. This method employed Sonogashira coupling and tandem addition-
Studies on the Structure and Stereochemistry of Cytotoxic Furanonaphthoquinones from Tabebuia impetiginosa: 5- and 8-Hydroxy-2-(1-hydroxyethyl)naphthofuran-4,9-diones
Fujimoto, Yoshinori,Eguchi, Tadashi,Murasaki, Chikako,Ohashi, Yuji,Kakinuma, Katsumi,et al.
, p. 2323 - 2327 (2007/10/02)
Chemical investigation of the bark of Tabebuia impetiginosa (Bignoniaceae) afforded cytotoxic furanonaphthoquinones, including 5-hydroxy-2-(1-hydroxyethyl)naphthofuran-4,9-dione and its 8-hydroxy isomer.The position of the phenolic group in these two compounds was established by X-ray crystallography.The furanonaphthoquinones were found to be mixtures of both enantiomers in different proportions, i.e., (for the 5-hydroxy isomer) R:S 1:23 and (for the 8-hydroxy isomer) R:S 3:1.The synthesis of the racemic naphthofurans, their optical resolution into enantiomerically pure forms, and the determination of their absolute stereochemistry are described.The structure of kigelinone was also established to be that of the 5-hydroxy isomer, not the 8-hydroxy one, through this study.
