905811-34-9Relevant academic research and scientific papers
Unified synthesis and cytotoxic activity of 8-O -methylfusarubin and its analogues
Vijitphan, Pongsit,Rukachaisirikul, Vatcharin,Muanprasat, Chatchai,Iawsipo, Panata,Panprasert, Jiraporn,Tadpetch, Kwanruthai
, p. 7078 - 7087 (2019/08/01)
A simple and unified synthesis of four related pyranonaphthoquinone natural products, e.g. 8-O-methylfusarubin, 8-O-methylanhydrofusarubin, fusarubin and anhydrofusarubin, is reported. The key synthetic features include the precedented Diels-Alder cycload
Products of an acetylation protocol on two pentaalkoxynaphthalenes
Giles, Robin G. F.,Green, Ivan R.,Van Eeden, Nester
, p. 1695 - 1706 (2007/10/03)
The benzyl and isopropyl groups were evaluated as O-protecting entities in 1,2,4,5,8-pentaalkoxynaphthalene systems upon treatment with a proven acetylation protocol. Only the benzyl group demonstrated moderate stability. Copyright Taylor & Francis Group,
