23022-74-4Relevant academic research and scientific papers
Palladium-catalyzed C-H functionalization of pyridine N-oxides: Highly selective alkenylation and direct arylation with unactivated arenes
Seung, Hwan Cho,Seung, Jun Hwang,Chang, Sukbok
supporting information; scheme or table, p. 9254 - 9256 (2009/02/03)
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
Beckmann and cyclization reactions of δ-oxo-α,β- unsaturated ketoximes obtained from pyrylium salts and hydroxylamine. Formation of 2-aryl(or alkyl)amino-4,6- disubstituted pyrylium salts
Uncuta, Cornelia,Tudose, Adriana,Caproiu, Miron Teodor,Plaveti, Marieta,Kakou-Yao, Rita
, p. 15011 - 15024 (2007/10/03)
The reaction of 2,4,6-trisubstituted pyrylium salts 1 with hydroxylamine gave regio- and stereo-selectively 1,3,5- trisubstituted 2-cis-pentene-1,5-dione 1-oximes 4. On cyclization, 3,5,5-trisubstituted 2-isoxazolines 6 and 2,4,6- trisubstituted pyridine 1-oxides 5 were obtained, originating in the anti/syn stereoisomers of oxime 4, respectively. Beckmann reaction of keto-ketoximes 4 with thionyl chloride unexpectedly gave 2-aryl (or alkyl)amino-4,6-disubstituted pyrylium salts 7, the first example of rearrangement/cyclization involving carbonylic oxygen as terminator. Crystallographic data are provided for (Z)-N-t-butyl-3,6,6-trimethyl-2-heptenecarboxamide 13b.
