The Role of Asymmetric Synthesis in Drug Discovery

Asymmetric Synthesis of Pharmacologically Active Spirooxindoles

Author(s): Chanchal Vashisth, Prabhjot Kaur, Urmila Berar and Neera Raghav *

Pp: 47-73 (27)

DOI: 10.2174/9798898812676125010006

* (Excluding Mailing and Handling)

Abstract

Spirooxindoles are a class of organic compounds characterized by a spirocyclic framework, where an oxindole moiety (which is a structure containing an indole fused to a carbonyl group) is connected to another ring system via a spiro carbon atom. These compounds have attracted significant interest in medicinal chemistry due to their diverse biological activities. They have been studied for their potential as anticancer, anti-inflammatory, and antimicrobial agents. The structural diversity of spirooxindoles allows for a wide range of pharmacological activities, making them valuable scaffolds in drug design. This chapter compiles the recent synthetic schemes on asymmetric synthesis of spirooxindoles and their significance as potential drug candidates. It discusses the different synthetic routes used to prepare chiral spirooxindoles and highlights the impact of chirality on their biological activities.


Keywords: Asymmetric synthesis, Biological activities, Chiral, Medicinal chemistry, Spirooxindoles.

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