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Nucleophilic substitution of azines

The azinones and their reaction characteristics are discussed in some detail in Section II, E. Because of their dual electrophilic-nucleophilic nature, the azinones may be bifunctional catalysts in their own formation (cf. discussion of autocatalysis below) or act as catalysts for the desired reaction from which they arise as byproducts. The uniquely effective catalysis of nucleophilic substitution of azines has been noted for 2-pyridone. [Pg.193]

B. Activation by Azine-Nitrogen and Other Factors in the Nucleophilic Substitution of Azines. 172... [Pg.145]

The third volume of this series covers three specific groups of compounds the carbolines (reviewed by R. A. Abramovitch and I. D. Spenser), the thiatriazoles (K. A. Jensen and C. Pedersen), and the pentazoles (I. Ugi). The remaining four chapters deal with topics of general chemical interest from the heterocyclic viewpoint the quaternization of heterocyclics (G. F. Duffin), carbene reactions (C. W. Rees and C. E. Smithen), applications of the Hammett equation (H. H. Jaffe and H. Lloyd Jones), and some aspects of the nucleophilic substitution of heterocyclic azines (G. Rluminati). [Pg.427]

Kinetic Data on Nucleophilic Substitution of Bicyclic Azines... [Pg.146]

It is quite reasonable to expect the bimolecular two-stage mechanism Sj Ar ) to predominate in most aromatic nucleophilic substitutions of activated substrates. However, only in rare instances is there adequate evidence to rule out the simultaneous occurrence or predominance of other mechanisms. The true significance of the alternative mechanisms in azines needs to be determined by trapping the intermediates or by applying modem separation and characterization methods to the identification of at least the major portion of the products, especially in kinetic studies. [Pg.152]

A bifunctional reagent such as ethanolamine can favor ortho substitution of azines due to hydrogen bonding as in 62. With a bifunctional nucleophile such as ethylene glycol anion, facilitation of... [Pg.183]

Nucleophilic substitution of bicyclic azines can be summarized by the following generalizations ... [Pg.308]


See other pages where Nucleophilic substitution of azines is mentioned: [Pg.182]    [Pg.196]    [Pg.215]    [Pg.182]    [Pg.196]    [Pg.215]    [Pg.182]    [Pg.196]    [Pg.215]    [Pg.100]    [Pg.107]    [Pg.354]    [Pg.182]    [Pg.196]    [Pg.215]    [Pg.182]    [Pg.196]    [Pg.215]    [Pg.182]    [Pg.196]    [Pg.215]    [Pg.100]    [Pg.107]    [Pg.354]    [Pg.147]    [Pg.167]    [Pg.217]    [Pg.305]    [Pg.320]    [Pg.380]    [Pg.383]    [Pg.303]    [Pg.390]    [Pg.316]    [Pg.147]    [Pg.167]    [Pg.195]    [Pg.217]    [Pg.305]    [Pg.308]    [Pg.310]   


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Nucleophilic substitution of azines, activation by azine-nitrogen

Nucleophilic substitution of bicylic azines, kinetic data

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