Published in Tetrahedron Letters
A new, concise synthesis of the CCR-5 receptor antagonist maraviroc (UK-427,857) from 3-phenyl-1-propanol has been completed in four steps featuring a site-selective C–H functionalization.
Graduate Student July 2010 - February 2016
L'Université de Princeton (Princeton, NJ US)
Worked for Professor Erik J. Sorensen as a member of the NSF-CCI Center for Selective C-H Functionalization, focusing on the synthesis of complex natural products utilizing C-H functionalization.