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Pyridine continued structure

Directed metallation continues to be developed as a convenient method for regiospecific substitution of pyridines. A mild and general procedure for the preparation of structurally diverse 4-alkyl-2-aminopyridines 37 involves the lithiation/alkylation of aminopyridine derivative 36 <96JOC(61)4810>. [Pg.228]

The monoketone bis(2,2, /V,/V -bipyridyl)ketone forms a [CoinL2]+ complex on reaction with [Co(NH3)4(C03)]+ in water.981 As reported for a quite different Co11 complex, the ketone is hydrated to form the gem diol which binds as a monodeprotonated O-donor along with the two pyridine groups in a tridentate chelate, with very little distortion from octahedral observed in the complex. This appears to represent a facile route for this type of inherently poor donor to achieve coordination. Chelated /3-diketonate anions are long-studied examples of O-donor chelates, and continue to be examined. A simple example is the m-[Co(acac)2(NH 3)2]1 (acac = 2,4-pentane-dionate), structurally characterized and utilized to produce molecular mechanics force field parameters for /3-diketones bound to Co111.982... [Pg.86]

Figure 7. LEED pattern and structure of pyridine at Pt(lll). A. LEED pattern of PYR adsorbed at Pt(lll), 51 eV. Continued on next page. Figure 7. LEED pattern and structure of pyridine at Pt(lll). A. LEED pattern of PYR adsorbed at Pt(lll), 51 eV. Continued on next page.
Cyclohexaamylose continued) mono-6-O-tosyl-, preparation of, 23 250 pyridine-2,5-dicarboxylic acid derivative, catalytic action of, 23 251 separation of, by complexing, 23 214 structure, stereochemistry and physical properties of, 23 210-213... [Pg.85]

Dewar and Maitlis143 discussed quite successfully the course of nitration in series of pyridine-like heterocycles in terms of the Dewar reactivity numbers. There is a continuing interest in the electronic structure of pyridine65, 144-140 a model of this compound has been studied by the ASP MO LCAO SCF (antisymmetrized products) method in the 77-electron approxition.146 The semi-empirical parameters146 were obtained from the most recent values of ionization potentials and electron affinities, and bicentric repulsion integrals were computed theoretically. [Pg.97]


See other pages where Pyridine continued structure is mentioned: [Pg.305]    [Pg.161]    [Pg.318]    [Pg.55]    [Pg.95]    [Pg.175]    [Pg.290]    [Pg.226]    [Pg.122]    [Pg.47]    [Pg.697]    [Pg.1509]    [Pg.167]    [Pg.145]    [Pg.466]    [Pg.130]    [Pg.239]    [Pg.679]    [Pg.163]    [Pg.7]    [Pg.35]    [Pg.297]    [Pg.9]    [Pg.46]    [Pg.191]    [Pg.183]    [Pg.81]    [Pg.204]    [Pg.366]    [Pg.145]    [Pg.142]    [Pg.143]    [Pg.466]    [Pg.215]    [Pg.318]    [Pg.940]    [Pg.45]    [Pg.192]    [Pg.718]    [Pg.226]    [Pg.64]    [Pg.191]    [Pg.425]    [Pg.63]    [Pg.398]   
See also in sourсe #XX -- [ Pg.3 ]




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Continuous structure

Pyridine structure

Pyridines—continued

Structure [continued)

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