155953-31-4Relevant articles and documents
Reactions of Cyclic 1,3-Dicarbonyl Compounds with 1,2(1,4)-Dihydro-1-methyl-2(4)-methylene-N-heterocycles. A New Access to 6,12-Methano-dibenz-oxazocinones
Henning, Hans-Georg,Thanh, Le Hoang,Laue, Joerg,Urban, Barbara,Reck, Guenter
, p. 95 - 106 (1994)
The enamine-type methylene-N-heterocycles 1-5 react with cyclic 2-ethoxymethylene-1,3-dicarbonyl compounds 6 to give 2--1,3-dicarbonyl componds 7-14.The result of the reactions between 1,2-dihydro-1-methyl-2-methylene-quinoline (1a) and cyclic 1,3-dicarbonyl compounds depends on the nature of the dihydro intermediates A/B.Dehydrogenation of keton intermediates A results in 2-(1,2-dimethyl-4(1H)-quinolylidene)-1,3-dicarbonyl compounds 17-21.Enol intermediates B with 6-membered dicarbonyl ring form 6,12-methano-dibenzoxazocinones 22-25. 1H NMR spectra and X-ray structure analysis prove the structure of 23. - Keywords. 2--1,3-dicarbonyl compounds; 2-(1,2-Dimethyl-4(1H)-quinolylidene)-1,3-dicarbonyl compounds; 6,12-Methano-dibenzoxazocinones; X-ray analysis.