4.7 Article

Synthesis of Weinreb amides using diboronic acid anhydride-catalyzed dehydrative amidation of carboxylic acids

Journal

CHEMICAL COMMUNICATIONS
Volume 56, Issue 86, Pages 13145-13148

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cc05630h

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Funding

  1. JSPS KAKENHI [19K07000]
  2. Grants-in-Aid for Scientific Research [19K07000] Funding Source: KAKEN

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The first successful example of the direct synthesis of Weinreb amides using catalytic hydroxy-directed dehydrative amidation of carboxylic acids using the diboronic acid anhydride catalyst is described. The methodology is applicable to the concise syntheses of eight alpha -hydroxyketone natural products, namely, sattabacin, 4-hydroxy sattabacin, kurasoins A and B, soraphinols A and B, and circumcins B and C.

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