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Gynocardin

Ci8H20BrNOl0S C3H60 6-0-(p-Bromophenylsulfonyl)gynocardin, acetone solvate BGYNOC 30 465... [Pg.398]

Gynocardin is a naturally occurring cyanogenic glycoside having the structure shown. What cyanohydrin would you expect to be formed on hydrolysis of gynocardin, and to what ketone does this cyanohydrin correspond ... [Pg.742]

Raubbnheimer, D., Cyanoglycoside gynocardin from Acraea horta (L.) (Lepidoptera Acraeinae), J. Chem. Ecol., 15, 2177-2189 (1989). [Pg.298]

Hydrolysis product of gynocardin. Syrup. Dextrorotatory. Does not reduce FehUnga. Forms cryst. Ba salt. Hot dil. HgSO —> glucose -1- a carboxylic acid (outntne aalt m.p. 224° decomp.). [Pg.145]

Power F B, Gornall F H 1904 Gynocardin, a new cyanogenetic glucoside. Preliminary note. Proc Chem Soc (London) 20 137... [Pg.297]

Spencer K C, Seigler D S 1984 Gynocardin from Passiflora. Planta Med 50 356-357... [Pg.298]

Compounds responsible for this specific odour, in addition to other components, are the degradation products of cyanogenic glycoside gynocardin with a cyclopentene ring (see Section 10.3.2.3.1). [Pg.117]

Gynocardin p-Glucose 1S,4S,5R Gynocardia, Pangium, Taractogenes, Rawsonia... [Pg.788]

See other pages where Gynocardin is mentioned: [Pg.199]    [Pg.49]    [Pg.704]    [Pg.727]    [Pg.465]    [Pg.284]    [Pg.285]    [Pg.285]    [Pg.289]    [Pg.296]    [Pg.596]    [Pg.596]    [Pg.1058]    [Pg.1136]    [Pg.145]    [Pg.145]    [Pg.703]    [Pg.283]    [Pg.295]    [Pg.296]    [Pg.787]    [Pg.787]    [Pg.789]    [Pg.91]    [Pg.94]   
See also in sourсe #XX -- [ Pg.49 ]

See also in sourсe #XX -- [ Pg.704 , Pg.727 ]

See also in sourсe #XX -- [ Pg.742 ]

See also in sourсe #XX -- [ Pg.285 , Pg.289 , Pg.298 ]

See also in sourсe #XX -- [ Pg.703 ]

See also in sourсe #XX -- [ Pg.283 ]

See also in sourсe #XX -- [ Pg.105 , Pg.775 , Pg.776 ]



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