Producción Científica Profesorado

Novel Route to Ynamides: Stable Ligands Equivalent to Unstable Oxazol-4-Ylidenes.



Mendoza Espinosa, Daniel

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.






Artículos relacionados

Firsttotalsyntheses of dihydroflustramine C and flustramine E, alkaloids from the marine bryozoan Fl...

Role of lipid peroxidation in biliary obstruction in the rat

Synthesis of Bromoindole Alkaloids from Laurencia brongniartii

Unimolecular rearrangements of ketene-O,O-acetals and fragmentations occurring in the gas phase

Transesterifications mediated by t-BuNH2

First Total Synthesis of ()-Flustraminol B

Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2

Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling

Regioselective Synthesis of 3-Indolyl(alkoxy)acetates

Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives