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Synthesis of derivatives of 6H-1,2-oxazine by cyclization of ketoximes with derivatives of terminal acetylene compounds

机译:酮肟与末端乙炔化合物衍生物的环化反应合成6H-1,2-恶嗪衍生物

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摘要

A new series of 6H-1,2-oxazines were synthesized by the reaction of ketones with hydroxylamine hydrochloridein the presence of sodium acetate to give ketoximes 1(a-e). Chloramine-T was used as an effective reagent forthe generation of α-nitrosolefins from ketoximes 1(a-e) which subsequently underwent hetero Diels-Alderreaction with terminal acetylenes 4(a-d), to give 6H-1,2-Oxazine derivatives 5(a-t).
机译:在乙酸钠存在下,酮与盐酸羟胺反应,合成了一系列新的6H-1,2-恶嗪,得到酮肟1(a-e)。氯胺-T被用作从酮肟1(ae)生成α-亚硝基烯烃的有效试剂,酮肟1(ae)随后与末端乙炔4(ad)进行杂Diels-Alder反应,得​​到6H-1,2-恶嗪衍生物5(at) 。

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