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.
Regioselective Synthesis of 3-Indolyl(alkoxy)acetates
Trapping enols of esters and lactones with diazomethane
Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine
One-potsynthesis of conformationallyrestrictedspirooxindoles
Transesterifications mediated by t-BuNH2
Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2
Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives
Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters