4.8 Article

Catalytic Ortho-Acetoxylation of Masked Benzyl Alcohols via an Exo-Directing Mode

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ORGANIC LETTERS
卷 17, 期 11, 页码 2696-2699

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b01098

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  1. CPRIT
  2. Welch Foundation [F-1781]
  3. ACS PRF
  4. NSF [CHE-1003947]

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A Pd-catalyzed ortho-acetoxylation of masked benzyl alcohols to synthesize various 2-hydroxyalkylphenol derivatives is reported. The 2,6-dimethoxyl benzaldoxime proved to be an efficient exo-type directing group for arene (sp(2)) CH functionalization. Two strategies were demonstrated to remove the directing group through N-O and C-O bond cleavages. A high catalyst turnover (>1000) was obtained to illustrate the practicality of this method.

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