342783-28-2Relevant articles and documents
Kumar, Rahul,Ravi, Chitrakar,Rawat, Deepa,Adimurthy, Subbarayappa
supporting information, p. 1665 - 1673 (2018/04/24)
An efficient access to 2,3-diarylimidazo[1,2-a]pyridines via silver(I)-catalyzed C-H bond functionalization
Khoshneviszadeh, Mehdi,Soheilizad, Mehdi,Fardpour, Maryam,Mahdavi, Mohammad
, p. 1817 - 1821 (2017/09/26)
Abstract: An efficient and economic Ag-catalyzed method for the direct cross-coupling of unactivated imidazo[1,2-a]pyridines with arylboronic acids has been developed. This approach leads to the formation of corresponding 2,3-diarylimidazo[1,2-a]pyridine derivatives as biological and pharmaceutical materials of interest in good yields under mild reaction conditions. Graphical abstract: [Figure not available: see fulltext.].
Straightforward synthesis of various 2,3-diarylimidazo[1,2-a]pyridines in peg400 medium through one-pot condensation and C-H arylation
Hiebel, Marie-Aude,Fall, Yacoub,Scherrmann, Marie-Christine,Berteina-Raboin, Sabine
, p. 4643 - 4650 (2014/08/05)
PEG400 is described herein as a suitable medium for the condensation of various 2-amino pyridines with α-bromo ketones. 2-Arylimidazo[1,2-a]pyridines were synthetized in a short time through microwave irradiation in moderate to excellent yields
