Recent advances in decarbonylative annulation reactions

In recent years, decarbonylative annulation reactions have emerged as one of the most efficient routes to construct a variety of important carbocyclic and heterocyclic scaffolds. The main advantages of this type of reaction are, first, the carbonyl compounds are used as the starting materials which are abundant in nature and second, the major by-product of this reaction is carbon monoxide. In the last two decades, various intramolecular and intermolecular decarbonylative annulation reactions have been performed using carbonyl compounds and alkenes/alkynes/arenes/isocyanates etc. as the annulation partners. These reactions are typically performed either in the presence of or in the absence of a metal catalyst. However, these reactions are still in their infancy as a very little progress has been achieved in these reactions. Through this review article, it is attempted to highlight the recent developments on various decarbonylative annulation reactions which ultimately lead to the formation of important structural moieties.

Automated summary

In recent years, decarbonylative annulation reactions have become an efficient route for constructing important carbocyclic and heterocyclic scaffolds. The main advantages include the use of abundant carbonyl compounds as starting materials and the production of carbon monoxide as a major by-product. Despite being in their infancy, these reactions show promising potential for forming important structural moieties.