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Plasmodial pigment

Similar insoluble oxidants were also used in the preparation of volatile, unstable polyene aldehydes during work on the plasmodial pigment fuligorubin A," while comparable solution-phase oxidants were markedly less successful (scheme 18.2). [Pg.54]

Synthesis of physarorubinic acid, which is a polyenoyltetramic acid plasmodial pigment, is another example. The synthesis uses a Lacey-Dieckmann cyclization starting with ester 51, followed by deprotection to give physarorubinic acid (52) in 78% yield for the two steps. ... [Pg.106]

See other pages where Plasmodial pigment is mentioned: [Pg.6]    [Pg.147]    [Pg.240]    [Pg.240]    [Pg.235]    [Pg.6]    [Pg.147]    [Pg.240]    [Pg.240]    [Pg.235]    [Pg.172]    [Pg.172]    [Pg.59]    [Pg.292]    [Pg.1964]   
See also in sourсe #XX -- [ Pg.54 ]



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