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Synthesis of multisubstituted quinolines from Baylis-Hillman adducts obtained from substituted 2-chloronicotinaldehydes and their antimicrobial activity
Authors:Narender P  Srinivas U  Ravinder M  Rao B Ananda  Ramesh Ch  Harakishore K  Gangadasu B  Murthy U S N  Rao V Jayathirtha
Affiliation:Organic Chemistry Division-II, Indian Institute of Chemical Technology, Tarnaka, Hyderabad.
Abstract:Baylis-Hillman acetates were synthesized from substituted 2-chloronicotinaldehydes and were conveniently transformed into multisubstituted quinolines and cyclopenta[g]quinolines on reaction with nitroethane or ethyl cyanoacetate via a successive S(N)2'-S(N)Ar elimination strategy. Thus, synthesized quinolines were evaluated for antimicrobial activity and found having substantial antibacterial and antifungal activity.
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