An Ir–Pt Catalyst for the Multistep Preparation of Functionalized Indoles from the Reaction of Amino Alcohols and Alkynyl Alcohols
comunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7053
comunitat-uji-handle3:10234/8639
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http://dx.doi.org/10.1002/chem.201001180 |
Metadades
Títol
An Ir–Pt Catalyst for the Multistep Preparation of Functionalized Indoles from the Reaction of Amino Alcohols and Alkynyl AlcoholsData de publicació
2010Editor
Wiley-VCHISSN
0947-6539Cita bibliogràfica
Chemistry - A European Journal (2010), 16, 44, p. 13109–13115Tipus de document
info:eu-repo/semantics/articleVersió de l'editorial
http://onlinelibrary.wiley.com/doi/10.1002/chem.201001180/abstractParaules clau / Matèries
Resum
The 1,2,4-trimethyltriazolylidene (ditz) ligand allows the preparation of homo- and heterodimetallic complexes of Pt2 and Ir–Pt. These two complexes have been characterized by means of spectroscopic and diffractommetric ... [+]
The 1,2,4-trimethyltriazolylidene (ditz) ligand allows the preparation of homo- and heterodimetallic complexes of Pt2 and Ir–Pt. These two complexes have been characterized by means of spectroscopic and diffractommetric techniques. The catalytic activity of these complexes, together with that of other Pt-based compounds, has been explored in the cyclization–addition of alkynyl alcohols and indoles. The Ir–Pt complex [{PtI2(py)}(μ-ditz){IrI2(Cp*)}] (py=pyridine; Cp*=pentamethylcyclopentadienyl) allows the combination of an iridium-mediated oxidative cyclization of 2-(ortho-aminophenyl)ethanol to form indoles, with a further step employing a Pt-based multistep reaction that functionalizes indoles. Our results show that the Ir–Pt complex is a very active catalyst in this new multistep preparation of functionalized indoles from the reaction of an amino alcohol with alkynyl alcohols [-]
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Copyright © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
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