2012
Ung, G.; Mendoza-Espinosa, D.; Bertrand G. Novel Route to Ynamides: Stable Ligands Equivalent to Unstable Oxazol-4-Ylidenes. Chem. Commun. 2012, 48, 7088-7090.
Abstract
Deprotonation of an oxazolium salt induces a ring opening process leading to the corresponding ynamide. Although the expected mesoionic carbene is not obtained, the acyclic ynamide readily reacts with various transition metals yielding robust mesoionic carbene complexes.
Synthesis of Indolylindolines Mediated by tert-BuNH2
Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2
Regioselective Synthesis of 3-Indolyl(alkoxy)acetates
Synthesis of 6-bromo-2-arylindoles using 2-iodobenzoic acid as precursor
Role of lipid peroxidation in biliary obstruction in the rat
Synthesis of Acetamido(indol-3-yl)propanol Derivatives
Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters
First Total Synthesis of ()-Flustraminol B
Synthesis of Bromoindole Alkaloids from Laurencia brongniartii