Selectivity in the chemistry of oxygen-centered radicals - The formation of carbon-oxygen bonds

In recent years, powerful new methods for the generation of alkoxyl radicals under mild and neutral conditions have been developed. This progress has led to a thorough investigation of most O-radical elementary reactions. Today, sufficiently reliable thermodynamic and kinetic data are available either from experimental or from theoretical studies in order to predict alkoxyl radical reactivities and selectivities in synthesis. For instance, alkoxyl radicals readily add to carbon-carbon and carbon-nitrogen double bonds, Due to generally low activation barriers and strongly negative reaction enthalpies, inter- and intramolecular addition reactions proceed under kinetic control and are associated with high rate constants. Nevertheless, intramolecular 5-exo-trig additions, i.e. cyclizations, proceed with an astonishing degree of diastereoselectivity and often provide complementary selectivities if compared to commonly used methods such as the bromine cyclization of alkenols. Therefore, several useful applications of O-radical cyclizations in the synthesis of functionalized tetrahydrofurans have been discovered in the last few years. A second major reaction channel of alkoxyl radicals is associated with the homolysis of a beta-C-C bond. This fragmentation proceeds under thermodynamic control and affords a carbonyl compound besides an alkyl radical from the starting alkoxyl radical. Regioselectivities for C-C bond homolysis may be predicted by considering strain release (cyclic carbon framework) and the stability of the newly formed carbon radical (cyclic and open chain carbon skeletons). The third major group of alkoxyl radical-based transformations are connected with homolytic substitutions such as intramolecular 1,5-hydrogen shifts which have been applied with considerable success to remote functionalization reactions, In view of the diversity of alkoxyl radical reactions it is the aim of this review to organize basic principles of this type of chemistry and to present its latest useful application in organic synthesis. 1 Introduction 2 General Aspects 3 Elementary Reactions 4 Generation of Oxygen-Centered Radicals and their Application in Chain Reactions 5 Addition of O-Radicals to Multiple Bonds 5.1 Intramolecular Addition to Carbon Carbon Double Bonds 5.2 Intermolecular Addition to Double Bonds 6 Formation of Carbonyl Compounds (beta-C-C Cleavage) 7 Rearrangements 8 Hydrogen Abstractions: Remote Functionalizations and Subsequent Nucleophilic Transformations 9 Summary and Perspectives