首页> 外文期刊>Tetrahedron >REACTIONS OF 7-METHOXYIMINO-4-METHYLCHROMENE-2,8-DIONE WITH PHOSPHINES - PREPARATION OF N-SUBSTITUTED 7-AMINO-8-HYDROXY-4-METHYL-2H-[1]-BENZOPYRAN-2-ONES
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REACTIONS OF 7-METHOXYIMINO-4-METHYLCHROMENE-2,8-DIONE WITH PHOSPHINES - PREPARATION OF N-SUBSTITUTED 7-AMINO-8-HYDROXY-4-METHYL-2H-[1]-BENZOPYRAN-2-ONES

机译:7-甲氧基亚氨基-4-甲基亚甲基-2,8-二酮与膦的反应-N-取代的7-氨基-8-羟基-4-甲基-2H- [1]-苯并吡喃-2-酮的制备

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摘要

7-Methoxyimino-4-methylchromene 2,8-dione 2 reacts with triarylphosphines 1(a-d) to give the unexpected 7-arylamino-8-hydroxy-4-methyl-2H-[1]-benzopyran-2-ones 7(a-d) and methyl diarylphosphinates 8(a-d) in high yields. The reaction of 2 with trialkylphosphines 1(e,f) as well as with diphenylphosphine 15 leads to the formation of the N-dialkylphosphinoyl derivatives 11, 12, 14 and the N-diphenylphosphinoyl derivative 19, along with compounds 7(e,f). The methylation of compounds 7a, 7f, 11 and 19 is also studied and reaction mechanisms to explain the formation of the products obtained are suggested. Copyright (C) 1996 Elsevier Science Ltd [References: 12]
机译:7-甲氧基亚氨基-4-甲基色烯2,8-二酮2与三芳基膦1(ad)反应生成意外的7-芳基氨基-8-羟基-4-甲基-2H- [1]-苯并吡喃-2-酮7(ad )和高产率的二芳基次膦酸甲酯8(ad)。 2与三烷基膦1(e,f)以及与二苯基膦15的反应导致形成N-二烷基膦酰基衍生物11、12、14和N-二苯基膦酰基衍生物19以及化合物7(e,f) 。还研究了化合物7a,7f,11和19的甲基化,并提出了反应机理来解释所得产物的形成。版权所有(C)1996 Elsevier Science Ltd [参考:12]

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