2403-01-2Relevant articles and documents
Regioselective Three-Component Reaction of Pyridine N-Oxides, Acyl Chlorides, and Cyclic Ethers
Jones, D. Heulyn,Kay, Steven T.,McLellan, Jayde A.,Kennedy, Alan R.,Tomkinson, Nicholas C. O.
supporting information, p. 3512 - 3515 (2017/07/17)
A novel three-component reaction of pyridine N-oxides, acyl chlorides, and cyclic ethers is described. Treatment of an electron-deficient pyridine N-oxide with an acyl chloride in the presence of a cyclic ether at 25-50 °C leads to a substituted pyridine as a single regioisomer in up to 58% isolated yield. Isotopic-labeling experiments and substrate scope support the reaction proceeding through a carbene intermediate.
OXIDATIVE DEMETHYLATION OF SOME METHYLNITROPYRIDINE 1-OXIDES
Achremowicz, Lucjan
, p. 2433 - 2434 (2007/10/02)
3-Nitropyridine 1-oxide and 5-methyl-3-nitropyridine 1-oxide are produced readily by oxidative demethylation using SeO2 of 2-methyl- and 2,5-dimethyl-3-nitropyridine 1-oxides.