4.6 Article

Organocatalytic aminocarbonylation of α,β-unsaturated ketones with N,N-dimethyl carbamoylsilane

期刊

NEW JOURNAL OF CHEMISTRY
卷 45, 期 16, 页码 7256-7260

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d1nj00782c

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资金

  1. National Natural Science Foundation of China [21662029]
  2. Young Scientists Foundation of Shihezi University [2015ZRKXJQ05]
  3. Excellent Young Teachers Plan of Bingtuan [2017CB001, CZ027203]
  4. International Cooperation Project of Shihezi University [GJHZ201801]

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An organic superbase-catalyzed aminocarbonylation reaction of alpha,beta-unsaturated ketones was reported, leading to the synthesis of alpha-siloxyamides or alpha-hydroxyamides in good yields.
An organic superbase-catalyzed aminocarbonylation reaction of alpha,beta-unsaturated ketones was reported. Under the catalysis of 10 mol% Schwesinger's superbase t-Bu-P-4, a variety of enones and ynones reacted with N,N-dimethyl carbamoylsilane to afford alpha-siloxyamides or alpha-hydroxyamides in 56-82% yields.

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