By R. A. Abramovitch
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139" Properties 26 26 24 24 Ref. Me 0 N ON3 Compound I 0- 0- 3-PyNi, C1; NaN, Method o f preparation TABLE VIII-8. p. p. p. p. )" Ref. Properties 'Identical IR spectra b- 0- b- b- 0- 0- Method of preparation 0- Compound TABLE VIII-8. p. p. p. p. 89-90" Ref. Properties VI N ~ 0 ~~ \ N- o NO, r"ph = 0, - NaNO, aq. p. p. p. p. p. p. p. p. 126-128" 2-PyNH1, PhNO, aq. NaOH ~ Properties ~~~ Method of preparation "'"0 EtO N kN) N=NPh Compound ~ TABLE VIII-9. Preparation and Properties of Azopyridines 27 27 4 53 Ref.
Reactions . . . . . . . . . . . . . A. Oxidation B. Reactions with Aldehydes and Ketones . . . C. Acylation . . . . . . . . . . . a. Carbonyl Derivatives b. Sulfonyl Derivatives . . . . . . . . . . c. Ureas, Amidines . . . . . D. Diazotization Reactions E. Nuclear Substitution Reactions . . . . . . . . F. Synthesis of Polycyclic Systems a. Naphthyridines . . . . . b. Pyridopyrimidine . . . . . c. Diazaindenes . . . . . . d. Carbolines .
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