Concise synthesis of an enantiopure bicyclic pyrazinone as constrained peptidomimetic building block†
Vincent Gembus,Solenn Janvier,Jean-Pierre Lecouvé,Lucile Vaysse-Ludot,Jean-François Brière,Vincent Levacher
Organic & Biomolecular Chemistry Pub Date : 01/06/2012 00:00:00 , DOI:10.1039/C2OB06762E
Abstract

A concise synthetic route has been developed for the preparation of a constrained peptidomimetic pyrazinone building block. From hydroxy-L-lysine, the desired pyrazinone is obtained in 43% overall yield (6 steps) via an efficient deprotection–double cyclization sequence.

Graphical abstract: Concise synthesis of an enantiopure bicyclic pyrazinone as constrained peptidomimetic building block