苄胺
肟
过渡金属
催化作用
化学
组合化学
药物化学
有机化学
作者
P. R. Lakshmi,Sunanda Kumari Kadiri,Varaprasad Bodala,Y. Bharathi Kumari,Satish Kumar Kotyada,Vidavalur Siddaiah
标识
DOI:10.1002/slct.202304447
摘要
Abstract An efficient TBHP/TBAI mediated strategy has been developed for the synthesis of 2,4,6‐trisubstitued pyridines from ketoxime acetates and benzylamines under metal‐free conditions for the first time. In this protocol benzylamine acts as an effective ArCO surrogate. This methodology features use of inexpensive catalysts, avert of additional ligands and additives and high functional group tolerance. Moreover, 5‐Lipoxygenase enzyme inhibitory activities were performed for all synthesised compounds. Among all 2,4,6‐trisubstituted pyridines 3fg, 3fa and 3eg showed good activity.
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