Selective Oxidative Cleavage of the C–C Bond in α,β-Epoxy Ketone into Carbonyl Compounds
Author:
Affiliation:
1. Green Catalysis Center, College of Chemistry, Zhengzhou University, Daxue Road 75, 450052 Zhengzhou, China
Funder
Henan Province
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acsomega.2c01464
Reference29 articles.
1. A Domino Approach for the Synthesis of α -Iodo-β -dicarbonyl Compounds from α -Epoxycarbonyls
2. Ring opening of α,β-epoxy phenyl ketones with ceric ammonium nitrate (CAN) and potassium bromide
3. Ionic Liquid as Reagent. A Green Procedure for the Regioselective Conversion of Epoxides to Vicinal-Halohydrins Using [AcMIm]X under Catalyst- and Solvent-Free Conditions
4. NaOH-Catalyzed Thiolysis of α,β-Epoxyketones in Water. A Key Step in the Synthesis of Target Molecules Starting from α,β-Unsaturated Ketones
5. An Easy Procedure for the Highly Regioselective Conversion of Epoxides to Halohydrins
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