Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Quinones with Extended Unbranched Side Chains

Quinones with Extended Unbranched Side Chains [Pg.183]

A colourless compound, betulachrysoquinone hemiketal (413), which must be related biogenetically to the sarcodontic acids, has been isolated from wood of Betula lutea inoculated with Phanerochaete chry- [Pg.183]

It is a mixture of the ceriporiones-A (415) and -B (416) which imparts a cherry red colour to the acetone extracts of Ceriporia viridans 155). The mixture [m.p. 149-150 °C Rf 0.46, silica gel (benzene ethyl formate formic acid = 10 5 3)], which has not been separated into its individual components, exhibited absorption maxima at 303 and 463 nm and formed a green monoanion with ammonia, and a blue dianion with aqueous potassium hydroxide. The structures (415) and (416) were deduced from and C-n.m.r. spectra while bearing in mind biogenetic considerations. The position of the side chain double bonds in these pigments, however, awaits further confirmation. [Pg.184]

The ceriporiones are closely related to the antibiotic merulinic acids, e.g. merulinic acid-A (417), which have been isolated from fruit bodies of Merulius tremellosus and Phlebia radiata 275). [Pg.184]


Quinones with Extended Unbranched Side Chains.183... [Pg.2]




SEARCH



Extended-chain

Quinones extended

Unbranched

© 2024 chempedia.info