Palladium-Catalyzed C−H Functionalization of Pyridine N-Oxides: Highly Selective Alkenylation and Direct Arylation with Unactivated Arenes
Journal of the American Chemical Society2008Vol. 130(29), pp. 9254–9256
Citations Over TimeTop 1% of 2008 papers
Abstract
Two catalytic protocols of the oxidative C-C bond formation have been developed on the basis of the C-H bond activation of pyridine N-oxides. Pd-catalyzed alkenylation of the N-oxides proceeds with excellent regio-, stereo-, and chemoselectivity, and the corresponding ortho-alkenylated N-oxide derivatives are obtained in good to excellent yields. Direct cross-coupling reaction of pyridine N-oxides with unactivated arene was also developed in the presence of Pd catalyst and Ag oxidant, which affords ortho-arylated pyridine N-oxide products with high site-selectivity.
Related Papers
- → Reactivity of 4‐nitropyridine‐N‐oxide: Preparation of 4‐substituted derivatives of pyridine‐N‐oxide and pyridine(1951)73 cited
- → Pyridine‐N‐oxide as an intermediate for the preparation of 2‐ and 4‐substituted pyridines(1950)64 cited
- → Thermochemical study of the trans- and cis-isomeric forms of 4-(4-methoxystyryl)pyridine N-oxide(2017)1 cited
- → Synthesis of pyridine bases from piperidine derivatives(1977)2 cited
- → The action of p‐toluenesulphonyl chloride on pyridine‐n‐oxide (III)(1961)10 cited