Preparations of Anthraquinone and Naphthoquinone Derivatives and Their Cytotoxic Effects
…, R Saito, T Kubo, D Kon, Y Hirano, S Saito
Index: Cui, Xing-Ri; Saito, Ryota; Kubo, Takatsugu; Kon, Daijiro; Hirano, Yuich; Saito, Setsuo Chemical and Pharmaceutical Bulletin, 2011 , vol. 59, # 3 p. 302 - 314
Full Text: HTML
Citation Number: 2
Abstract
Chrysophanol and 1, 8-di-O-hexylchrysophanol derivatives having nucleic acid bases at position 5 were synthesized. Furthermore, derivatives of menadione substituted at position 11 (type A naphthoquinone derivatives) or methylmenadione substituted at position 7 (type B naphthoquinone derivatives) modified with nucleic acid bases, amines and thiocyano, selenocyano or thioacetyl groups were synthesized. The cytotoxic effects of these ...
Related Articles:
Asymmetric Diels–Alder addition of cyclopentadiene to chiral naphthoquinones
[Brimble, Margaret A.; McEwan, John F.; Turner, Peter Tetrahedron Asymmetry, 1998 , vol. 9, # 7 p. 1239 - 1255]
[Brimble, Margaret A.; Duncalf, Letecia J.; Reid, David C. W.; Roberts, Tabitha R. Tetrahedron, 1998 , vol. 54, # 20 p. 5363 - 5374]
[Tetrahedron, , vol. 57, # 48 p. 9743 - 9748]
Selenium (IV) oxide catalyzed oxidation of aldehydes to carboxylic acids with hydrogen peroxide
[Synthetic Communications, , vol. 30, # 24 p. 4425 - 4434]
Preparations of Anthraquinone and Naphthoquinone Derivatives and Their Cytotoxic Effects
[Chemical and Pharmaceutical Bulletin, , vol. 59, # 3 p. 302 - 314]