Demonstration of reversible CC bond cleavage in oxiranylcarbinyl radicals
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Allyloxy Radicals are Formed Reversibly from Oxiranylcarbinyl Radicals: A Kinetic Study
2. The Photolysis of Organic Nitrites. V. Intramolecular Alkoxide Radical Addition to A Double Bond
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4. Intramolecular β,γ-addition of allylic alkoxyl radicals. A new general synthesis of α-iodoepoxides by photolysis of allylic alcohol hypoiodites in the presence of mercury(II) oxide, iodine and pyridine in benzene
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1. Facile rearrangements of a vinylogous α-hydroxy-β-dicarbonyl substrate involving an apparent oxirane C–C bond scission;Tetrahedron Letters;2015-11
2. Selectfluor-Mediated Simultaneous Cleavage of C–O and C–C Bonds in α,β-Epoxy Ketones Under Transition-Metal-Free Conditions: A Route to 1,2-Diketones;The Journal of Organic Chemistry;2015-06-15
3. Chemoselective CC Bond Cleavage of Epoxide Motifs: Gold(I)-Catalyzed Diastereoselective [4+3] Cycloadditions of 1-(1-Alkynyl)oxiranyl Ketones and Nitrones;Chemistry - A European Journal;2010-12-01
4. ChemInform Abstract: Demonstration of Reversible C-C Bond Cleavage in Oxiranylcarbinyl Radicals.;ChemInform;2010-08-03
5. Oxiranes and Oxirenes: Monocyclic;Comprehensive Heterocyclic Chemistry III;2008
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