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Decevinic acid

On oxidation with chromic acid in dilute sulphuric acid, cevine produces an acid fraction, which on heating at 180° gives a good yield of decevinic acid, C14H14O, m.p. 273-8° (dec.), [a] f° 47-6° (pyridine). [Pg.703]

The lactonetricarboxylic acid, CuHigOg, on heating to 200° is converted into an acid, CigHuOe, which has been named decevinic acid. [Pg.302]

The many and in part obscure reactions of this acid are summarized in Table 13. It has not been possible to interpret these reactions to arrive at a satisfactory structure for decevinic acid. Since it is formed from the lactone, C14H18O8, by a reaction or reactions that are also not understood, the many experimental results are at present of no service in elucidating the structure of cevine (6, 7, 11). [Pg.306]

Decamine, K27 Decevinic acid, K35 Decinine, K27 Decodine, K27 Decursinol, Y1 1,2-dehydroaspidospermidine,... [Pg.303]

See other pages where Decevinic acid is mentioned: [Pg.303]    [Pg.303]    [Pg.221]    [Pg.363]    [Pg.363]    [Pg.363]    [Pg.775]    [Pg.160]    [Pg.208]    [Pg.303]    [Pg.303]    [Pg.221]    [Pg.363]    [Pg.363]    [Pg.363]    [Pg.775]    [Pg.160]    [Pg.208]   
See also in sourсe #XX -- [ Pg.35 ]



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