Nucleophilic addition to 2, 3-pyridyne and synthesis of benzonaphthyridinones
Y Fang, RC Larock
Index: Fang, Yuesi; Larock, Richard C. Tetrahedron, 2012 , vol. 68, # 13 p. 2819 - 2826
Full Text: HTML
Citation Number: 16
Abstract
Download PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... A study of the nucleophilic addition of amines to 2,3-pyridyne has been carried out. 2-Aminopyridines have been generated exclusively. A series of benzonaphthyridinones have been synthesized by reacting 2,3-pyridyne and o-aminobenzoates.
Related Articles:
[Iwasaki, Genji; Saeki, Seitaro; Hamana, Masatomo Chemistry Letters, 1986 , p. 31 - 34]
SAR analysis of a series of acylthiourea derivatives possessing broad-spectrum antiviral activity
[Burgeson, James R.; Moore, Amy L.; Boutilier, Jordan K.; Cerruti, Natasha R.; Gharaibeh, Dima N.; Lovejoy, Candace E.; Amberg, Sean M.; Hruby, Dennis E.; Tyavanagimatt, Shanthakumar R.; Allen III, Robert D.; Dai, Dongcheng Bioorganic and Medicinal Chemistry Letters, 2012 , vol. 22, # 13 p. 4263 - 4272]