70932-71-7Relevant articles and documents
Synthesis and biological activity of cocaine analogues. 2. 6H-[2]benzopyrano[4,3-c]pyridin-6-ones
Lazer,Hite,Nieforth,Stratford
, p. 845 - 849 (1979)
1,2,3,4-Tetrahydro-2-methyl-6H-[2] benzopyrano[4,3-c]pyridin-6-one (20) and cis- and trans-1,2,3,4,4a, 10b-hexahydro-2-methyl-6H-2[2]benzopyrano[4,3-c]pyridin-6-one (3a and 3b) were synthesized. The design of 3b was based on the proposal that the active c
Facile synthesis of 4-alkoxycarbonylisoquinoline-1,3-diones and 5-alkoxycarbonyl-2-benzazepine-1,3-diones via a mild alkaline cyclization
Billamboz, Muriel,Bailly, Fabrice,Cotelle, Philippe
experimental part, p. 392 - 398 (2009/09/08)
(Chemical Equation Presented) A series of 4-methoxycarbonylisoquinoline-1, 3-diones was obtained from homophthalic acid in four steps. The key step was the quantitative and rapid alkaline cyclization of 2-methoxycarbonyl-2-(2- methoxycarbonylphenyl) aceta