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C4H7n Pyrroline

Ornithine-Derived Alkaloids. Ornithine (23) undergoes biological decarboxylation reductively to generate either putrescine [110-60-1] (36), c4h12n2, or its biological equivalent, and subsequent oxidation and cyclization gives rise to the pyrroline [5724-81-2], (37), C4H7N. [Pg.535]

Pyrroline, 2,5-Dihydro-1 H-pyr role. C4H7N mol wt 69,10, C 69.527°, H 10.217., N 20.27%. Prepd by uduction of pyrrole with zinc and glacial acetic or hydrochloric acid. [Pg.1275]

See other pages where C4H7n Pyrroline is mentioned: [Pg.19]    [Pg.31]    [Pg.100]    [Pg.107]    [Pg.112]    [Pg.17]    [Pg.29]    [Pg.98]    [Pg.105]    [Pg.110]    [Pg.276]    [Pg.55]    [Pg.213]    [Pg.520]    [Pg.213]    [Pg.222]    [Pg.520]    [Pg.17]    [Pg.105]    [Pg.110]    [Pg.276]    [Pg.19]    [Pg.31]    [Pg.100]    [Pg.107]    [Pg.112]    [Pg.17]    [Pg.29]    [Pg.98]    [Pg.105]    [Pg.110]    [Pg.276]    [Pg.55]    [Pg.213]    [Pg.520]    [Pg.213]    [Pg.222]    [Pg.520]    [Pg.17]    [Pg.105]    [Pg.110]    [Pg.276]    [Pg.366]    [Pg.377]    [Pg.377]    [Pg.378]    [Pg.378]    [Pg.589]    [Pg.331]    [Pg.319]    [Pg.330]   
See also in sourсe #XX -- [ Pg.9 , Pg.90 ]



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Pyrroline

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