Quine

Quin L D and Verkade J G (eds) 1994 Phosphorus-31 NMR Spectral Properties in Compound Characterization and Structural Analysis (New York VCH)... 

Excellent yields of the former product are also obtained with quinoline N-oxide. Improved yields of Reissert compounds are found under phase-transfer conditions (29). The regiochemistry of the method changes dramatically with /V-alkyl quin olinium salts, eg, /V-methy1quino1inium iodide [3947-76-0] (12), which form 4-cyanoquinoline [23395-72-4] (13) (30), through the intermediary in this example of A[-methyl-4-cyano-l,4-dihydroquinoline... 

Composite resins can be cured using a variety of methods. Intraoral curing can be done by chemical means, where amine—peroxide initiators are blended in the material to start the free-radical reaction. Visible light in the blue (470—490 nm) spectmm is used to intraoraHy cure systems containing amine—quin one initiators (247). Ultraviolet systems were used in some early materials but are no longer available (248). Laboratory curing of indirect restorations can be done by the above methods as well as the additional appHcation of heat and pressure (249,250). 

However, the preparation of l-nitroanthraquiQone-2-carboxyhc acid has the difficulties mentioned previously. Therefore, new processes for preparing this compound not from the 1-nitro compound but from other precursors have been iatensively studied. 1-Amin oanthra quin one derivatives have been proposed for this purpose (90). 

A Methylanthrapyridone and Its Derivatives. 6-Bromo-3-methylanthrapyridone [81-85-6] (75) is an important iatermediate for manufacturiag dyes soluble ia organic solvents. These solvent dyes are prepared by replacing the bromine atom with various kiads of aromatic amines. 6-Bromo-3-methylanthrapyridone is prepared from 1-methyl amino-4-bromoanthra quin one (43) by acetylation with acetic anhydride followed by ring closure ia alkaU. The startiag material of this route is anthraquiaoae-l-sulfonic acid (16). 

Benzanthrone Dyes. Vat dyes derived from benzanthrone may be divided into two groups violanthrones and isoviolanthrones, dyes that have the perylene ring in their molecular stmcture and benzanthrone pyrazolanthrones and benzanthrone acridones, the peri ring closure products of 3-anthra quin onyl amino-ben zanthrone. 

Finally the preformed 2-formyl-3-aminoquinoxaline (448) gave the pyrido[2,3-f ]quin-oxalin-2-one (449) with activated esters/sodium alkoxide (79ZC422). 

Thenyl bromide and 2-pyridinealdehyde reacted to form a quaternary salt (182) which was cyclodehydrated to thieno(2,3-b)quin-azolinium bromide (183). ... 

Alkylquinazolines are catalytically reduced to the corresponding 3,4-dihydro derivatives/ The only example of a 4-substituted quin-azoline which was reduced to its 3,4-dihydro derivative is 2-chloro-4-phenylquinazoline which gave 4-phenyl-3,4-dihydroquinazoline/ 4-Methylquinazolines are susceptible to oxidation, as is shown by the attempted nitration of 2,4-diraethylquinazoline which causes the removal of the methyl group with formation of 4-hydroxy-2-methyl-6-nitroquinazoline/ When the 4-substituent is —C(Et) (C02Et)2 recrystallization of the picrate from ethanol is sufficient to convert it to 4-hydroxyquinazoline/ Similar hydrolyses occur in acid solution and the mechanism undoubtedly involves a hydrated intermediate/... 

Dihydroquinazolines are also products of the reaction of quin-azoline with nucleophilic reagents (see Section II,B). 

Little work has been reported on pyrazine-2,3-diones, however spectral evidence has been advanced by HonzL to support the dioxo formulation 126. Dioxo structures have been assigned to quin-oxaline-2,3-dione (127) and its 1-methyl analog on the basis of ultraviolet and infrared spectral data, and according to... 

In those few cases where hydration and pseudobase formation parallel each other, the agreement can be traced to the fortuitous circumstance that the structure and electronic configuration of the molecule permit both phenomena to occur simultaneously. Quin-azoline-3-methochloride, one of these rare examples, is discussed in Section III,C, 1. 

---