Rearrangements and Fragmentations Mediated by Hypervalent Iodine Reagents
Author:
Affiliation:
1. Department of Chemistry; Temple University; Philadelphia PA 19122 USA
2. Laboratoire de Méthodologie et Synthèse de Produits Naturels; University of Quebec at Montreal; Montreal H3C 3P8 Quebec Canada
Publisher
John Wiley & Sons, Ltd
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/9780470682531.pat0953/fullpdf
Reference114 articles.
1. Advances in Synthetic Applications of Hypervalent Iodine Compounds
2. Activated Iodosylbenzene Monomer as an Ozone Equivalent: Oxidative Cleavage of Carbon−Carbon Double Bonds in the Presence of Water
3. Iodomesitylene-Catalyzed Oxidative Cleavage of Carbon−Carbon Double and Triple Bonds Using m-Chloroperbenzoic Acid as a Terminal Oxidant
4. Reactivity of Hydroxy- and Aquo(hydroxy)-λ3-iodane-Crown Ether Complexes
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1. Chemoselective cycloisomerization of O-alkenylbenzamides via concomitant 1,2-aryl migration/elimination mediated by hypervalent iodine reagents;Communications Chemistry;2023-06-17
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