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CHEM01200604012 Dibakar Goswami - Homi Bhabha National ...

CHEM01200604012 Dibakar Goswami - Homi Bhabha National ...

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Extensive research on natural products chemistry especially with an eye to drug<br />

development has led to the isolation of myriads of bioactive compounds and also<br />

identification of suitable pharmacophore for their potential medicinal values. These<br />

compounds often bear a complex structure and possess chirality. Hence, even at the height<br />

of maturity, synthetic organic chemistry is facing the challenge to design and develop<br />

efficient syntheses for such functionally enriched complex biologically active compounds.<br />

This warrants facile, atom economic, high yielding and selective organic reactions. Given<br />

the importance of stereochemistry in bio-recognition, the issue of asymmetric synthesis has<br />

become overwhelming in modern organic synthesis. In view of these, the present work is<br />

focused on the development of operationally simple and practically viable asymmetric<br />

strategies that include some metal-catalyzed asymmetric routes and non-conventional<br />

protocols, and their possible application to the enantiomeric syntheses of a few chosen bioactive<br />

molecules. Accordingly the content of the thesis is presented in four chapters as<br />

detailed below.<br />

Chapter I:<br />

Introduction to Asymmetric Synthesis<br />

This chapter deals with broad reviews on asymmetric synthesis, 1 the major focus<br />

of the present investigation. The salient features of the deliberation include the genesis and<br />

importance of chirality, and different methods of enantiomeric synthesis with special<br />

emphasis on asymmetric transformations. The aspect of using chiral compounds as<br />

building blocks for the synthesis of enantiomerically pure compounds is discussed<br />

subsequently. The influences of substrate, reagent, catalyst and auxiliary to direct the<br />

asymmetric transformation have also been elaborately explained. Finally, the theoretical<br />

ii

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