Alkane Carbon−Hydrogen Bond Functionalization with (NHC)MCl Precatalysts (M = Cu, Au; NHC = N-Heterocyclic Carbene)
Organometallics2006Vol. 25(9), pp. 2237–2241
Citations Over TimeTop 10% of 2006 papers
Abstract
Facile alkane functionalization by means of the insertion of :CHCO2Et, from ethyl diazoacetate, into carbon−hydrogen bonds mediated by catalytic amounts of (NHC)MCl (NHC = N-heterocyclic ligand; M = Cu, Au) and a halide scavenger MX has been achieved. This chemistry includes the insertion of the carbene fragment into alkane primary positions with Cu- and Au-based catalysts. The nature of the counterion X and of the NHC ligand have a significant effect on the overall yields and regioselectivity of the reaction.
Related Papers
- → N‐Heterocyclic Carbene‐Catalyzed Umpolung of Alkynyl 1,2‐Diketones(2017)31 cited
- → PhI(OAc)2-promoted umpolung acetoxylation of enamides for the synthesis of α-acetoxy ketones(2017)21 cited
- → Organocatalytic Umpolung Strategies: Beyond Classical Reactivity Patterns(2022)2 cited
- → Cover Feature: Efficient One‐Pot Multifunctionalization of Alkynes en Route to α‐Alkoxyketones, α‐Thioketones, and α‐Thio Thioketals by using an Umpolung Strategy (Chem. Eur. J. 57/2017)(2017)
- → ChemInform Abstract: Synthesis of Bridged Benzazocines and Benzoxocines by a Titanium‐Catalyzed Double‐Reductive Umpolung Strategy.(2015)