114864-23-2Relevant articles and documents
Microwave-assisted multicomponent synthesis of aza-, diaza-, benzo-, and dibenzofluorenedione derivatives
Defant, Andrea,Guella, Graziano,Mancini, Ines
, p. 3003 - 3016 (2008)
A microwave procedure was efficiently applied to the synthesis of a series of heteropolycyclic compounds with known or potential biological activities. Antitumor amide 3was obtained in a few minutes and with high yields through a solventless, one-pot cyclization, followed by treatment with the suitable amine. This method was also used to access tetracyclic aza-compounds 5/6, where their selective formation as N,N-syn and N,N-anti regioisomers was investigated under a solventless condition, or by changing the solvent, in the presence of solid supports and a catalytic amount of ecofriendly metal salts. Thermal access to similar polycyclic compounds recently reported under conventional heating by using the preformed pyridinium or isoquinolinium ylides was improved in this instance by microwave irradiation and extended to the synthesis of diaza-esters. In any case, the one-pot, three-component cyclization was more atom-efficient than the N-ylide sequence. Copyright Taylor & Francis Group, LLC.
Copper(II)-catalyzed synthesis of benzo[ f ]pyrido[1,2- a ]indole-6,11-dione derivatives via naphthoquinone difunctionalization reaction
Liu, Yun,Sun, Jin-Wei
experimental part, p. 1191 - 1197 (2012/03/11)
Benzo[f]pyrido[1,2-a]indole-6,11-diones have been synthesized in high yields by copper(II)-catalyzed three-component reactions of acyl bromide, 1,4-naphthoquinone, and pyridine (or isoquinoline) via sp2-C-H difunctionalization of naphthoquinone
