Increasing synthetic efficiency via direct C–H functionalization: Formal synthesis of an inhibitor of botulinum neurotoxin
Document Type
Article
Date of Original Version
4-4-2011
Abstract
A new and efficient scheme for the synthesis of one of the best known inhibitors of botulinum neurotoxin serotype A (BoNTA) is reported herein. The synthetic route involves two palladium-catalyzed C–H functionalization reactions, formally activating three C–H bonds. © 2011 The Royal Society of Chemistry.
Publication Title, e.g., Journal
Chemical Communications
Volume
47
Issue
16
Citation/Publisher Attribution
Potavathri, Shathaverdhan, Abhishek Kantak, and Brenton Deboef. "Increasing synthetic efficiency via direct C–H functionalization: Formal synthesis of an inhibitor of botulinum neurotoxin." Chemical Communications 47, 16 (2011): 4679-4681. doi: 10.1039/c1cc10755k.
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