Bromonitroalkenes as efficient intermediates in organic synthesis

Abstract

Bromonitroalkenes are useful molecules in synthetic organic chemistry. They are mainly prepared from nitroalkenes via bromination reactions. In this review, the application of bromonitroalkenes as partners in the reaction with a diversity of mono- and bi-functional molecules, including aldehydes and ketones, active methylene compounds, 1,2-dicarbonyls, enamines, enols, electron-rich arenes, amidines, azomethine ylides, azirines, diazo compounds, and many others, is reviewed. By using these substrates, various biologically active scaffolds, such as heterocycles, carbocycles, spirocycles, polycyclic systems, natural products, and other useful acyclic compounds, were prepared. In addition, due to their dielectrophilic character, electrophilic and nucleophilic character, and ability to participate in cycloaddition reactions, bromonitroalkenes were efficiently applied in asymmetric cascade/domino/tandem reactions catalyzed by chiral catalysts. In this manuscript, around 55 papers are summarized and discussed during the years 2000–2023.