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Pyridine iris

Eastham and Derwent474 have also studied the kinetics of the perchloric acid-catalyzed reaction of ethylene oxide with pyridine. In excess of pyridine the rate was found to be dependent on the Conor Titrations of ethylene oxide and perchloric add. Addition of stronger bases,. g. ammonia, triethylamine, or benzylamiae, depressed the vum of cleavage, presumably by competing with ethylene oxide for thr-available proton source, believed to be pyridinium perchlorate in this case. Other acids examined included nitric acid and hydroiodie irireaction rate depended to a certain extent... [Pg.169]

DMPA = N,N-dimethyl-4-pyridine-amine TBA = iri-M-butylamine DBU = 1,7-diazobicyclo [5.4.0]-undec-7ene DBN = 1,5-diazobicyclo ... [Pg.1219]

Irie, H., I. Katayama, Y. Mizuno et al. 1979. Thermolysis of oxime O-aUyl ethers A new method for synthesis of pyridine derivatives. Heterocycles 12 (6) 771—773. [Pg.354]


See other pages where Pyridine iris is mentioned: [Pg.229]    [Pg.229]    [Pg.113]    [Pg.113]    [Pg.1862]    [Pg.73]    [Pg.1861]    [Pg.202]    [Pg.292]    [Pg.113]   
See also in sourсe #XX -- [ Pg.4 , Pg.1031 ]




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