The Binuclear Iridium(II) Hydride Complex [(C5Me5)Ir(μ-H)]2: A Novel Base for Reversible Deprotonation of Acidic Organic Compounds and a Unique Catalyst for C−C Bond Cleavage of Aromatic 1,2-Diols and Michael Additions
- 24 May 2001
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 123 (24), 5812-5813
- https://doi.org/10.1021/ja010186h
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Alkali and Alkaline-Earth Metal Ketyl Complexes: Isolation, Structural Diversity, and Hydrogenation/Protonation ReactionsChemistry – A European Journal, 2000
- Transfer of Ketyls from Alkali Metals to Transition Metals. Formation and Diverse Reactivities of d-Block Transition-Metal KetylsOrganometallics, 1999
- Direct Measurement of Ultrafast Carbon−Carbon Cleavage Rates via the Subpicosecond Charge-Transfer Activation of PinacolsJournal of the American Chemical Society, 1998
- Ruthenium-catalyzed aldol and Michael reactions of nitriles. Carbon-carbon bond formation by .alpha.-C-H activation of nitriles.Journal of the American Chemical Society, 1995
- Reactions of transition metal dihydrogen complexesCoordination Chemistry Reviews, 1992
- Structures of transition-metal hydride complexesAccounts of Chemical Research, 1979