316155-87-0Relevant academic research and scientific papers
Synthesis and regioselective alkylation of 1,6- and 1,7-naphthyridines
Colandrea,Naylor
, p. 8053 - 8057 (2007/10/03)
A regioselective alkylation of naphthyridines 4a-d, through the action of ethylchloroformate and benzylstannane 5, afforded the benzyl substituted dihydronaphthyridines 3a-d. These key intermediates 3a-d were transformed into the desired targets 2a-d in seven steps. (C) 2000 Elsevier Science Ltd.
Isoquinoline-6-carboxamides as potent and selective anti-human cytomegalovirus (HCMV) inhibitors
Chan, Laval,Jin, Haolun,Stefanac, Tomislav,Wang, Wei,Lavallee, Jean-Francois,Bedard, Jean,May, Suzanne
, p. 2583 - 2586 (2007/10/03)
Structure-activity relationship studies on our newly identified anti-HCMV compounds, the 1,6-naphthyridines led to the identification of isoquinoline-6-carboxamides as potent and selective anti-HCMV agents.
