Ring Transformation of 1,3-Dinitroquinolizin-4-one with Enolate Anions
نویسندگان
چکیده
منابع مشابه
The Ring Transformation of 3-Methyl-5-nitropyrimidin-4(3H)- one
3-Methyl-5-nitropyrimidin-4(3H)-one readily reacts with carbonyl compounds to produce three kinds of ring transformations. The nitropyrimidinone behaves as the synthetic equivalent of activated diformylamine affording 3,5-difunctionalized 4-pyridones, 4,5disubstituted pyrimidines and functionalized 4-aminopyridines. It also behaves like α-nitroformylacetic acid to give 5,6-disubstituted 3-nitro...
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6-Methyl-2-phenyl-7H-Oxazolo [3,2-b] [1,2,4] triazine (1) undersent ting transformation on treatment with ammonia and primary amines to afford the corresponding imidazol [1,2-b][1,2,4] triazine (2). Treatment of (1) with hydrazine hydrate gave the corresponding 3-aryl-4H-1,2,4- triazino [4,3-b][1,2,4] triazin-8 (1H)-one (3).
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The photoelectron spectra of the structural isomers of the three- and four-carbon enolate anions, n-C3H5O(-), i-C3H5O(-), n-C4H7O(-), s-C4H7O(-), and i-C4H7O(-) have been measured at 355 nm. Both the X(2A' ') ground and A(2A') first excited states of the corresponding radicals were accessed from the X(1A') ground state of the enolate anions. The separation energies of the ground and first excit...
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ژورنال
عنوان ژورنال: Bulletin of the Chemical Society of Japan
سال: 1987
ISSN: 0009-2673,1348-0634
DOI: 10.1246/bcsj.60.1198