Applications of Transition-metal-catalyzed Asymmetric Allylic Substitution in Total Synthesis of Natural Products: An Update

Metal-catalyzed asymmetric allylic substitution (AAS) reaction is one of the most synthetically useful reactions catalyzed by metal complexes for the formation of carbon-carbon and carbon-heteroatom bonds. It comprises the substitution of allylic substrates with a wide range of nucleophiles or S(N)2 '-type allylic substitution, which results in the formation of the above-mentioned bonds with high levels of enantioselective induction. AAS reaction tolerates a broad range of functional groups, thus has been successfully applied in the asymmetric synthesis of a wide range of optically pure compounds. This reaction has been extensively used in the total synthesis of several complex molecules, especially natural products. In this review, we try to highlight the applications of metal (Pd, Ir, Mo, or Cu)-catalyzed AAS reaction in the total synthesis of the biologically active natural products, as a key step, updating the subject from 2003 till date.

Automated summary

Metal-catalyzed asymmetric allylic substitution (AAS) reaction is a useful synthetic method for the formation of carbon-carbon and carbon-heteroatom bonds with high enantioselectivity. It has been widely applied in total synthesis and natural product research.