4.8 Article

Catalyst-Free Selective Oxidation of Diverse Olefins to Carbonyls in High Yield Enabled by Light under Mild Conditions

Journal

ORGANIC LETTERS
Volume 21, Issue 19, Pages 7726-7730

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b02569

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Funding

  1. National Natural Science Foundation of China [U1610104, 21676046]

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The selective oxidation of olefins, in particular, aromatic olefins to carbonyls, is of significance in organic synthesis. In general, stoichiometric toxic oxidants or a high-cost catalyst is required. Herein we report a novel and practical light-enabled protocol for the synthesis of carbonlys in high yield through a catalyst-free oxidation of olefins using H2O2 as a clean oxidant. A broad scope of carbonyls can be synthesized in high yield, and no catalyst or toxic oxidant is required.

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