α-Acyloxylation of Ketones/Cyclic Ethers Mediated by Hypervalent Iodine(III) Reagents as Oxidants and Nucleophilic Sources-Reference-Cited by-同舟云学术

α-Acyloxylation of Ketones/Cyclic Ethers Mediated by Hypervalent Iodine(III) Reagents as Oxidants and Nucleophilic Sources

Published:2024-01-11 Issue:3 Volume:89 Page:2055-2063
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Jia Hao¹,Li Nan¹,Tang Chunmei¹,Ni Wenjing¹,Zhao Xinru¹,Sun Jing¹,Wu Fufang¹^ORCID,Shen Xiaobao¹,Zhai Hongbin²

Affiliation:

1. Biomass Oligosaccharides Engineering Technology Research Center of Anhui Province, Engineering Research Center of Biomass Conversion and Pollution Prevention of Anhui Educational Institutions, Fuyang Normal University, Fuyang 236037, China

2. Institute of Marine Biomedicine, Shenzhen Polytechnic, Shenzhen 518055, China

Funder

Science and Technology Foundation of Shenzhen City

Science, Technology and Innovation Commission of Shenzhen Municipality

National Natural Science Foundation of China

Shenzhen-Hong Kong Institute of Brain Science

Horizontal Cooperation Project of Fuyang Municipal Government

Natural Science Foundation of Higher Education Institutions in Anhui Province

Innovative drug design & development collaborative team

Shenzhen Fundamental Research Institutions

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02526

Reference48 articles.

1. Metal-Free Reductive Cleavage of C−O σ-bonds in Acyloin Derivatives by an Organic Neutral Super-Electron-Donor

2. Synthesis of Multisubstituted Furans, Pyrroles, and Thiophenes via Ynolates

3. Iodobenzene-Catalyzed α-Acetoxylation of Ketones. In Situ Generation of Hypervalent (Diacyloxyiodo)benzenes Using m-Chloroperbenzoic Acid

4. Manganese Ate Complexes as New Reducing Agents: Perfectly Regiocontrolled Generation and Reactions of the Manganese Enolates with Electrophiles

5. Ligand-Free Copper(I)-Catalyzed Benzylic Acyloxylation of 2-Alkylpyridines under Aerobic Conditions

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