Coupling of Internal Alkynes in TpMe2Ir Derivatives: Selective Oxidation of a Noncoordinated Double Bond of the Resulting Iridacycloheptatrienes
Rojas Lima, Susana
2003
Eleuterio Álvarez, Margarita Gómez, Margarita Paneque, Cristina M. Posadas, Manuel L. Poveda, Nuria Rendón, Laura L. Santos, Susana Rojas-Lima, Verónica Salazar, Kurt Mereiter and Caridad Ruiz. Coupling of internal alkynes in Tp Me2 Ir derivatives. Selective oxidation of non-coordinated double bond of the resultanting iridacycloheptetrienes. J. Am. Chem. Soc., 125, 1478-1479, (2003). Preprinted
Artículos relacionados
Preparation of N-aryl-substituted spiro-?-lactams via Staudinger cycloaddition
Structure-Activity Relationships for Inhibition of Cysteine Protease Activity and Development of Pla...
Synthesis and Study of Monomeric and Dimeric Boronates by Spectroscopic Methods and X-ray Crystallog...
Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reactio
Et3, and efficient Mediator for Xanthate Transfer Based Radical Processes.
Enantioselective synthesis of ?-amino acids. Part 11: Diastereoselective alkylation of chiral deriva...
3-Benzoyl-2-isopropyl-4-alkyloxazolidin-5-ones as Efficient and Inexpensive Sources of Enantiopure ?...
X-ray crystallographic study of neutral boron chelates with ?-diketones and tropolone
O-benzyl-N-(2-furoyl)thiocarbamate
ChemInform Abstract: Facile Preparation of [4.4]Metacyclophane- and [5.5]Paracyclophane-Type Macrocy...