Literature Review of Radical-Polar Crossover Reaction

Described are Radical-Polar Crossover (RPC) reactions, which have played an important role in the organic synthesis, but very few review articles previously mentioned this concept. Using both photoredox catalysis and non-photoredox catalysis can achieve the RPC transformation within a one-pot mechanism under very mild condition. Besides this, RPC reactions provide many practical advantages such as rapid increasing in molecular complexity and good functional group tolerance. Therefore, this potentially valuable reaction can provide a lot of research opportunities. Overall, the comparison of different authors’ views, critical analyses of the methods, and an overall summary of the literature will be described in this review. The purpose of this work is to narrate both photoredox RPC reactions and non-photoredox RPC reactions in a systematic fashion and to grasp the valuable point of view from different authors. Applications of RPC reactions to the pharmaceutical sciences and industry will be presented at the end

Stereocontrolled intramolecular ketone-olefin reductive coupling reactions promoted by samarium diiodide

The stereocontrolled intramolecular coupling of unsaturated β-ketoesters and β-ketoamides is reported. Good yields of highly substituted β-hydroxycyclopentanecarboxylates are generated in the process, with substantial and predictable stereochemical control at three contiguous stereocenters. Excellent stereochemical control is achieved over three stereocenters in the ittle reaction

Pd-Catalyzed Suzuki–Miyaura Cross-Coupling Reactions between Sulfamates and Potassium Boc-Protected Aminomethyltrifluoroborates

Sulfamates were studied as the electrophilic partners in the palladium-catalyzed Suzuki–Miyaura cross-coupling reaction with potassium Boc-protected primary and secondary aminomethyltrifluoroborates. A broad range of substrates was successfully coupled to provide the desired products. Complex molecules containing a new carbon–carbon bond and an aminomethyl moiety could be prepared through this developed method