Iodine-Mediated Oxidative Rearrangement of α,β-Unsaturated Diaryl Ketones: A Facile Access to 1,2-Diaryl Diketones
Author:
Affiliation:
1. Chemical Engineering & Process Development Division, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411008, India
2. Academy of Scientific and Innovative Research (AcSIR), New Delhi 110 025, India
Funder
University Grants Commission
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acsomega.9b00833
Reference73 articles.
1. Oxidative rearrangement of alkenes using in situ generated hypervalent iodine(III)
2. Oxidative rearrangements of arylalkenes with [hydroxy(tosyloxy)iodo]benzene in 95% methanol: a general, regiospecific synthesis of α-aryl ketones
3. Oxidative Rearrangement of Tertiary Allylic Alcohols Employing Oxoammonium Salts
4. Reactions of alkenes with [hydroxy(tosyloxy)iodo]benzene: stereospecific syn-1,2-ditosyloxylation of the carbon-carbon double bond and other processes
5. Catalytic Oxidative 1,2-Shift in 1,1′-Disubstituted Olefins Using Arene(iodo)sulfonic Acid as the Precatalyst and Oxone as the Oxidant
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