Iodine‐Mediated Nucleophilic Direct Oxidative α‐Acetoxylation and α‐Alkoxylation of Ketones
Author:
Affiliation:
1. D-207Discovery LaboratoryOrganic Synthesis and Process Chemistry DivisionCSIR-Indian Institute of Chemical Technology Hyderabad- 500 007 India
2. Academy of Scientific and Innovative Research (AcSIR) New Delhi 110025 India
Funder
Department of Science and Technology, Government of Kerala
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.201903028
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5. Solid state synthesis of 2-aroylbenzo[b]furans, 1,3-thiazoles and 3-aryl-5,6-dihydroimidazo[2,1-b][1,3]thiazoles from α-tosyloxyketones using microwave irradiation †
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1. I2/DMSO-mediated oxidative C–C and C–heteroatom bond formation: a sustainable approach to chemical synthesis;RSC Advances;2024
2. The O2-Mediated Cross-Dehydrogenative Coupling: Rose Bengal-Catalyzed Direct Oxidative α-Acyloxylation of Ketones;Organic Letters;2023-06-28
3. CBr 4 Promoted α‐Acyloxyation of β‐Keto Esters and β‐Diketones by Sodium Carboxylates;ChemistrySelect;2022-03-23
4. Copper‐Catalyzed Direct Oxidative α‐Alkoxylation of 4‐Isochromanones;European Journal of Organic Chemistry;2021-05-05
5. Hypervalent Iodine-Mediated Diastereoselective α-Acetoxylation of Cyclic Ketones;Frontiers in Chemistry;2020-07-10
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