
He will be starting a postdoc position in the same university from March 2014. Congratulations!!
A brief description of his PhD research is outlined below:
His research was focused on the design and development of novel synthetic methods
to construct complex molecular architectures and potential pharmaceutically
active agents. An organocatalytic or catalyst-free method is considered to be
superior to transition-metal-catalyzed synthetic pathways from greener
perspectives though the specific catalytic performance of transition- metals in
achieving the target is great in the recent time. Usefulness of
ethylenediammonium diacetate (EDDA) in the domain of cascade processes e.g.
aldol type/ hetero Diels-Alder reaction and Knoevenagel type/ hetero Diels
Alder reaction in the delivery of pyrano[3,2-a]carbazoles, cis-fused tetrahydroquinolines,
quinolines alkaloids has been particularly rewarding in the biological
investigation owing to their pharmacological properties. Catalyst-free thermal
Wolff rearrangement followed by addition of carbon nucleophile to ketenes and C
sp3-H activation followed by cross-coupling with aromatics were the
subjects in the synthetic investigation during the study. His postdoctoral
research activities will focus on C-H activation/ Cross-coupling.
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