1243802-89-2Relevant academic research and scientific papers
Intramolecular Heck reaction: A facile sequential one-pot synthesis of 1,2,3,4-tetrahydrobenzo[b][1,6]naphthyridines
Bharath Kumar Reddy, Puchakayala,Ravi, Kanakaraju,Mahesh, Kukkamudi,Leelavathi, Panaganti
, p. 4039 - 4043 (2018/10/09)
A simple and convenient sequential one-pot synthesis of 1,2,3,4-tetrahydrobenzo[b][1,6] naphthyridines has been developed. The reductive amination of 2-chloro-3-formylquinolines with various amines in the presence of sodium borohydride provided the corresponding secondary amines in high yields. Further, a sequential one-pot reaction involving N-allylation and intramolecular Heck type 6-exo-trig cyclization was performed on the secondary amines to afford a range of desired 1,2,3,4-tetrahydrobenzo[b][1,6]-naphthyridine derivatives in good to high yields.
Design and synthesis of 2-chloroquinoline derivatives as non-azoles antimycotic agents
Kumar, Suresh,Bawa, Sandhya,Drabu, Sushma,Panda, Bibhu P.
, p. 1340 - 1348 (2012/05/05)
A series of secondary amines (4-19) containing 2-chloroquinoline as lipophilic domain have been synthesizedbased on the structural requirements essential for allylamine/benzylamine antimycotics by nucleophilic substitutionreaction of 3-chloromethyl-2-chlo
