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.
Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives
Trapping enols of esters and lactones with diazomethane
The absoluteconfiguration of cuauhtemone and related compounds
Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling
Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters
Transesterifications mediated by t-BuNH2
One-potsynthesis of conformationallyrestrictedspirooxindoles
Regioselective Synthesis of 3-Indolyl(alkoxy)acetates
First Total Synthesis of ()-Flustraminol B
13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters