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13P-Hydroxymamanine

The previously isolated 13P-hydroxymamanine had its (7i ,9iS,l IR,13R) absolute stereochemistry resolved by X-ray analysis of the corresponding hydrobromide hydrate and it was postulated that its biosynthetic origin was the oxidative cleavage of the N-l/C-10 bond of (-)-baptifoline. Fig. (32) [217],... [Pg.267]

The structures of (+)-mamanine (80) and (+)-13P-hydroxymamanine (24) correspond to oxidative products derived from the Nj-Cjo cleavage of (-)-anagyrine... [Pg.539]

See other pages where 13P-Hydroxymamanine is mentioned: [Pg.267]    [Pg.152]    [Pg.153]    [Pg.580]    [Pg.153]    [Pg.267]    [Pg.152]    [Pg.153]    [Pg.580]    [Pg.153]   
See also in sourсe #XX -- [ Pg.267 ]

See also in sourсe #XX -- [ Pg.27 , Pg.267 ]

See also in sourсe #XX -- [ Pg.267 ]



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13P-Hydroxymamanine X-ray analysis

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