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Pyridines, polycyclic

Retro-Diels-Alder decompositions may be encountered in the fragmentation patterns of reduced polycyclic pyridine derivatives, as in 1,2,3,4-tetrahydroisoquinoline and its N- acetyl derivative (122) (78HCA1730). Other studies leading to details of tautomerism are discussed in the relevant section (2.04.4). [Pg.135]

Mirtazapine 105, a polycyclic pyridine derivative containing a pyridine ring fused with an azepine ring system, is an antidepressant <2006W02006/008302>. The piperidine derivatives paroxetine 106, alnespirone 107, and Azaloxan... [Pg.327]

Polycyclic pyridines and quinolines could be prepared via a Rh-catalyzed C-H functionalization process (eq 15). ... [Pg.689]

Heterocyclic aromatic compounds can be polycyclic as well A benzene ring and a pyridine ring for example can share a common side m two different ways One way gives a compound called quinoline the other gives isoquinoline... [Pg.460]

It is understandable that dihydro adducts should be formed by polycyclic compounds and not by benzene or pyridine, because the loss of aromatic resonance energy is smaller in the former than in the latter process, (c) When dibenzoyl peroxide is decomposed in very dilute solution (0.01 Af) in benzene, 1,4-dihydro biphenyl is produced as well as biphenyl, consistent with addition of the phenyl... [Pg.137]

The chemistry of these polycyclic heterocycles is just what you miglu expect from a knowledge of the simpler heterocycles pyridine and pyrrole Quinoline and isoquinoline both have basic, pyridine-like nitrogen atoms, anc both undergo electrophilic substitutions, although less easily than benzene Reaction occurs on the benzene ring rather than on the pyridine ring, and r mixture of substitution products is obtained. [Pg.951]

Although pyridines and quinolines were first produced during the carbonization of coal, they are now available by synthesis in quantities that far exceed those by the former. Phosphorylated ribosides of hydroxylated and aminated pyrimidines and purines make up the basic structure of ribonucleic and deoxyribonucleic acids. The polycyclic oxaarenes are plant metabolites, while thiaarenes are primarily important components of high-sulfur petroleum that must be removed. [Pg.523]

Chains that include aromatic rings (phenols, pyridines, etc.) are said to be polycyclic and are stiffer, harder and more stable than aliphatic chains. Polycarbonate is an example, being hard enough for use in eyeglass lenses. An extreme example is Kevlar fiber. [Pg.166]

From such silanol-functional cyclics, the polycyclic (ladder) siloxanes are made in a controlled manner. Thus, the reaction of (7-PrSi(0H)0)4 with ((-PrPhClSiO)2 in pyridine was described, leading to the formation of tetraphenyl tricyclic ladder siloxane. Dephenylchlorination with A1C13/HC1, and the hydrolysis allowed isolation of tetrahydroxyl tricyclic ladder siloxane in good yield. Using a similar reaction starting from tetrahydroxyl ladder siloxane, the first pentacyclic ladder siloxane was obtained.38 Abe et al. describe the synthesis of... [Pg.655]

Fluoropyridines form valuable starting materials for a range of disubstituted pyridines because, after lithiation, nucleophilic substitution of fluoride (sometimes via the N-oxide) can be used to introduce, say, N or O substituents as in 191 and 192 (Scheme 96). Subsequent annelations can allow complex polycyclic heteroaromatics to be constructed. ... [Pg.546]

To carry out MCRs of aminoazoles with aldehydes and cyclic CH-acids, the methods of green chemistry were also applied. For example, treatments of 3-methylisoxazol-5-amine and aromatic aldehydes with 1,3-cyclohexanedione, dimedone, 1,3-indanedione, or titronic acid were proceeded in water under micro-wave irradiation at 120°C [100] (Scheme 31). As a result, clean, efficient, and convenient procedures for the generation of polycyclic-fused isoxazolo[5,4-b] pyridines 71 were developed. An interesting fact is that, in the case of 1,3-cyclohexanedione, dihydropyridine s were obtained while in aU other cases only hetero-aromatized derivatives were isolated. No reason for this experimental fact was discussed in the article. [Pg.62]


See other pages where Pyridines, polycyclic is mentioned: [Pg.48]    [Pg.836]    [Pg.48]    [Pg.836]    [Pg.48]    [Pg.836]    [Pg.836]    [Pg.448]    [Pg.44]    [Pg.31]    [Pg.32]    [Pg.32]    [Pg.48]    [Pg.836]    [Pg.48]    [Pg.836]    [Pg.48]    [Pg.836]    [Pg.836]    [Pg.448]    [Pg.44]    [Pg.31]    [Pg.32]    [Pg.32]    [Pg.26]    [Pg.836]    [Pg.189]    [Pg.201]    [Pg.134]    [Pg.286]    [Pg.132]    [Pg.697]    [Pg.49]    [Pg.314]    [Pg.372]    [Pg.78]    [Pg.310]    [Pg.622]    [Pg.295]    [Pg.413]    [Pg.574]    [Pg.420]    [Pg.315]    [Pg.290]    [Pg.569]    [Pg.172]   
See also in sourсe #XX -- [ Pg.46 , Pg.47 , Pg.48 , Pg.49 ]




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Fused-polycyclic pyridines

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