Natural Product Synthesis: Amphidinolide E and Acetogenins - Mohapatra, Seetaram
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Natural product synthesis: Amphidinolide E and Acetogenins has been divided into two chapters and each chapter subdivided into sections. Chapter I describes the synthetic studies towards Amphidinolide E. The THF Core was synthesized stereoselectively by applying Mercury mediated cyclisation as the key steps. The diene chain of the molecule was synthesized following stille coupling reaction. Chapter II explains Synthesis of Various kind of acetogenins and the bis-THF core of Acetogenins was synthesized stereoselectively by mercury mediated cyclisation.

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Produktbeschreibung
Natural product synthesis: Amphidinolide E and Acetogenins has been divided into two chapters and each chapter subdivided into sections. Chapter I describes the synthetic studies towards Amphidinolide E. The THF Core was synthesized stereoselectively by applying Mercury mediated cyclisation as the key steps. The diene chain of the molecule was synthesized following stille coupling reaction. Chapter II explains Synthesis of Various kind of acetogenins and the bis-THF core of Acetogenins was synthesized stereoselectively by mercury mediated cyclisation.
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Autorenporträt
Dr. Seetaram Mohapatra is currently working as a lecturer in Ravenshaw University, Cuttack, Odisha. He obtained his Ph.D degree from National Chemical laboratory, Pune, India under the guidance of Dr. Mukund K. Gurjar in 2008. He has published eighteen research papers in International journal of repute in the area of natural product synthesis.