104202-16-6Relevant articles and documents
Direct sequential C3 and C1 arylation reaction of imidazo[1,5-a]pyridine catalyzed by a 1,10-phenanthrolinepalladium complex
Yamaguchi, Eiji,Shibahara, Fumitoshi,Murai, Toshiaki
supporting information; experimental part, p. 939 - 940 (2011/12/05)
The direct sequential arylation reaction at the C3 and C1 positions of imidazo[1,5-a]pyridines with a variety of aryl iodides catalyzed by [Pd(phen)2](PF6)2 is described. The reaction of unsubstituted imidazo[1,5-a]pyridine with various aryl iodides proceeded selectively at the C3 position to exclusively give the corresponding C3-arylated products. The one-pot double-arylation reaction at the C3 and C1 positions of unsubstituted imidazo[1,5-a]pyridine with different aryl groups was also achieved.
1H- and 13C-NMR spectra of 3-aryl-2-azaindolizines
Ashauer,Wolff,Haller
, p. 43 - 52 (2007/10/02)
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