首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >REACTIONS OF O-METHYL O-QUINONE MONOOXIMES WITH METHYL-, METHYLENE- AND METHINE-SUBSTITUTED AROMATIC COMPOUNDS - SYNTHESIS OF BENZO[D]OXAZOLE AND 1,4-BENZOXAZINE DERIVATIVES
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REACTIONS OF O-METHYL O-QUINONE MONOOXIMES WITH METHYL-, METHYLENE- AND METHINE-SUBSTITUTED AROMATIC COMPOUNDS - SYNTHESIS OF BENZO[D]OXAZOLE AND 1,4-BENZOXAZINE DERIVATIVES

机译:O-甲基O-喹诺酮单肟与甲基,亚甲基和亚甲基取代的芳族化合物的反应-合成苯并[D]恶唑和1,4-苯并恶嗪衍生物

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摘要

O-Methyl o-quinone monoxime 1 reacts thermally with compounds 2a-d or 6a,b or 7a,b to give mainly the corresponding 2-substituted phenanthroxazoles 3a-c and 8. The reaction of 1 with aromatic methylene compounds 10a-c affords the ketones 13a-c in moderate to high yields. Similar products are also obtained from the reaction of monoximes 15a,b with some of the above reactants. The unexpected products 5 and 20 are obtained from the reaction of 1 with 2-methylimidazole (2d) and with phenyloxirane (19) respectively, while the 4H-1,4-oxazine derivative 23 is obtained from the reaction of 1 with indene (21). [References: 22]
机译:O-甲基邻醌单肟1与化合物2a-d或6a,b或7a,b热反应,主要得到相应的2-取代的吩噻唑3a-c和8。1与芳族亚甲基化合物10a-c反应得到酮13a-c的产量中等至高。从一肟15a,b与一些上述反应物的反应中也获得了类似的产物。意外产物5和20分别由1与2-甲基咪唑(2d)和与苯基环氧乙烷(19)的反应获得,而4H-1,4-恶嗪衍生物23由1与茚(21的反应)获得。 )。 [参考:22]

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