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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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