2006
Synthesis of n4:p2-Exocyclic-Diene Iridium(I) Complexes Derived from 1,3-Oxazolidin-2-ones and their Transformation into Iridium(III) Derivatives by Reaction with a Phosphine and with Aldehydes. Verónica Salazar, Oscar R. Suárez-Castillo, Rosa Padilla, J. Carlos Macías P, Miguel Ángel Méndez-Rojas, Joaquín Tamariz, Adriana Benavides. DOI: 10.1021/om050582z
Abstract
The reaction of the dimer [Ir(?-Cl)(coe)2]2 with two exocyclic dienes like N-substituted 4,5-dimethylene-2-oxazolidinones a and b, and KTpMe2 yields derivatives of the composition TpMe2Ir(a or b) (1a,b). Derivative 1a reacts with Ph2PCCPPh2, with the formal oxidative addition of the diene moiety to the metal center and coordination of the phosphine in the ?1 mode. Derivatives 1a,b react with aromatic aldehydes to form the new compounds 3 (with benzaldehyde) and 4 (anisaldehyde), which contain an elaborated bidentate ligand formed by coupling of the two organic fragments (diene and aldehyde). The structures of compounds 3a,b have been determined by X-ray diffraction analysis.
Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2
Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea
One-potsynthesis of conformationallyrestrictedspirooxindoles
Transesterifications mediated by t-BuNH2
First Total Synthesis of ()-Flustraminol B
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Synthesis of Bromoindole Alkaloids from Laurencia brongniartii
Role of lipid peroxidation in biliary obstruction in the rat