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Rapid Access to Free Phenols by Photocatalytic Acceptorless Dehydrogenation of Cyclohexanones at Room Temperature

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Phenols are ubiquitous substructures in natural products and bioactive compounds. However, practical methods for the direct construction of phenols under mild conditions remains challenging. Herein, a photocatalytic acceptorless dehydrogenative aro-matization of cyclohexanones or cyclohexenones at room temperature has been developed. The reaction features the visible-light and cobalt co-catalyzed sequential dehydrogenation of in-situ formed enol silyl ethers, which are regarded as a challenging process. This operationally simple method enables the synthesis of a series of phenols with diverse substitution patterns from cyclohexanones or cyclohexenones. Moreover, diverse substituted 1,2-, 1,3-, and 1,4-benzenediols were obtained from cyclo-hexanediones, providing a general and straightforward method for the synthesis of phenols from simple starting materials un-der mild conditions
Title: Rapid Access to Free Phenols by Photocatalytic Acceptorless Dehydrogenation of Cyclohexanones at Room Temperature
Description:
Phenols are ubiquitous substructures in natural products and bioactive compounds.
However, practical methods for the direct construction of phenols under mild conditions remains challenging.
Herein, a photocatalytic acceptorless dehydrogenative aro-matization of cyclohexanones or cyclohexenones at room temperature has been developed.
The reaction features the visible-light and cobalt co-catalyzed sequential dehydrogenation of in-situ formed enol silyl ethers, which are regarded as a challenging process.
This operationally simple method enables the synthesis of a series of phenols with diverse substitution patterns from cyclohexanones or cyclohexenones.
Moreover, diverse substituted 1,2-, 1,3-, and 1,4-benzenediols were obtained from cyclo-hexanediones, providing a general and straightforward method for the synthesis of phenols from simple starting materials un-der mild conditions.

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