4.8 Article

Unconventional Passerini Reaction toward α-Aminoxy-amides

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ORGANIC LETTERS
卷 18, 期 24, 页码 6396-6399

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b03293

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资金

  1. Erasmus Mundus Scholarship
  2. NIH [1R01GM097082-01]
  3. Innovative Medicines Initiative [115489]
  4. European Union under MSC ITN Accelerated Early stage drug dIScovery (AEGIS) Grant [675555]
  5. Marie Curie Actions (MSCA) [675555] Funding Source: Marie Curie Actions (MSCA)

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The Passerini multicomponent reaction (P-3CR) toward the one-step synthesis of alpha-aminoxy-amide, by employing for the first time a N-hydroxamic acid component, has been reported. The sonication-accelerated, catalyst-free, simple, fast, and highly efficient Passerini reaction is used for the synthesis of diverse alpha-aminoxy-amides. The reaction is compatible with a vast range of aldehydes, isocyanides, and N-hydroxamic acids such as N-hydroxysuccinimides and phthalimides. The generated Passerini products can be easily converted into several follow-up products.

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