首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Synthesis of 2,4-bis(aryloxy)-1,5-diarylpentane-1,5-diones by base-mediated tandem reaction
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Synthesis of 2,4-bis(aryloxy)-1,5-diarylpentane-1,5-diones by base-mediated tandem reaction

机译:通过碱介导的串联反应合成2,4-双(芳氧基)-1,5-二芳基-1,5-二乙烯烃

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摘要

A new, practical, base-mediated method has been developed for the synthesis of 2,4-bis(aryloxy)-1,5-diarylpentane-1,5-diones by a tandem α-methylenation-Michael reaction through activation of two C-Cl bonds. This method permits the use of dichloromethane instead of dibromomethane as a source of one carbon atom for the α-methylenation reaction. The products are useful in syntheses of polysubstituted pyridines and methylenebisbenzofurans.
机译:通过激活2c,开发了一种新的,实用的基础介导的方法,用于通过串联α-甲基化 - 迈克尔反应来开发2,4-双(芳氧基)-1,5-二芳基戊烷-1,5-二酮 -cl债券。 该方法允许使用二甲甲烷而不是二溴甲烷作为α-甲基化反应的一个碳原子的源。 该产品可用于多助化吡啶和亚甲基双苯并呋喃的合成。

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  • 作者单位

    State Key Laboratory of Chemo/Biosensing and Chemometrics College of Chemistry and Chemical;

    State Key Laboratory of Chemo/Biosensing and Chemometrics College of Chemistry and Chemical;

    State Key Laboratory of Chemo/Biosensing and Chemometrics College of Chemistry and Chemical;

    State Key Laboratory of Chemo/Biosensing and Chemometrics College of Chemistry and Chemical;

    State Key Laboratory of Chemo/Biosensing and Chemometrics College of Chemistry and Chemical;

    Key Laboratory of Chemical Biology Traditional Chinese Medicine Research (Ministry of Education);

    State Key Laboratory of Chemo/Biosensing and Chemometrics College of Chemistry and Chemical;

    State Key Laboratory of Chemo/Biosensing and Chemometrics College of Chemistry and Chemical;

    State Key Laboratory of Chemo/Biosensing and Chemometrics College of Chemistry and Chemical;

    State Key Laboratory of Chemo/Biosensing and Chemometrics College of Chemistry and Chemical;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

    ketones; Michael additions; tandem reactions;

    机译:酮;迈克尔添加;串联反应;

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