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Natural Product Synthesis: Eunicin, Palauamide and asimitrin has been divided into three chapters and each chapter subdivided into following sections: Introduction, Experimental and Characterisation and General References. Chapter I describes the synthetic studies toward tricyclic cembranoids: a modular approach for the construction of the tricyclic, framework of eunicin. Chapter II deals with studies toward biologically active Palauamide. Chapter III discusses synthetic studies toward Asimitrin using chiral pool strategy.

Synthesis of indanone based spirocyclic molecules following 1,3-dipolar cycloaddition reaction consists of two chapter. Chapter I deals withone pot, three component synthesis of spiroindenoquinoxaline pyrrolidine fused nitrochromene derivatives following 1,3-dipolar cycloaddition. Chaapter II deals with one pot, three component 1,3-dipolar cycloaddition: Regio and diastereoselective synthesis of spiropyrrolidinyl indenoquinoxaline based chromene nitrile derivatives.