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Chemistry of Acyl Radicals

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This article is published in Chemical Reviews.The article was published on 1999-06-24. It has received 693 citations till now. The article focuses on the topics: Acylation.

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Photochemical Reactions as Key Steps in Organic Synthesis

TL;DR: Photochemical Electron-Transfer Reactions with a Catalytic Sensitizer 1068 6.1.1 Photochemical Extrusion of Small Molecules 1067 6.2.2 Photochemical Rearrangings 1061 4.4.3.
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Recent Advances in Radical C-H Activation/Radical Cross-Coupling.

TL;DR: This Review provides a brief and concise overview of the current status and latest methodologies using radicals or radical cations as key intermediates produced via radical C-H activation, which includes radical addition, radical cascade cyclization, radical/radical cross-coupling, coupling of radicals with M-R groups, and coupling ofradical cations with nucleophiles (Nu).
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Thiyl Radicals in Organic Synthesis

TL;DR: The thiol−olefin cooxidation process was applied to the total synthesis of antimalarial agent yingzhaosu A and was extended to include the more challenging 1,5-dienes, from which six-membered ring endoperoxides can be obtained.
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Catalytic Enantioselective Transformations Involving C-H Bond Cleavage by Transition-Metal Complexes.

TL;DR: This analysis comprehensively review all asymmetric transition-metal-catalyzed methodologies that are believed to proceed via an inner-sphere-type mechanism, with an emphasis on the nature of stereochemistry generation.
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Metal-Catalyzed Decarboxylative C–H Functionalization

TL;DR: An overview of the utility of decarboxylative C-H bond functionalization in the synthesis of various organic compounds, such as styrenes, chalcones, biaryls, and heterocycles, is offered, covering most of the recent advances.
References
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Hydrocarbon Bond Dissociation Energies

TL;DR: The best available values for homolytic bond dissociation energies (BDEs) of various classes of neutral compounds are considered in a review as mentioned in this paper, focusing on prototypical radicals whose heats of formation, formerly thought to be well in hand, have recently been called into serious question.
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A new method for the deoxygenation of secondary alcohols

TL;DR: In this paper, a general synthesis of O-cycloalkyl thioesters has been developed which gives access to O-cycle-alkyl seleno-formates and selenobenzoates.
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