SUBSTITUENT EFFECT OF 4- AND 5-SUBSTITUTED 2-ARYL-METHYLIDENEINDANE-1,3-DIONES ON FORMATION OF 5-OXO-1H-4,5-DIHYDROINDENO[1,2-<i>b</i>]PYRIDINES
DOI:
https://doi.org/10.1007/6936Ключевые слова:
7a, 10-diazacyclohepta[def]fluorene, dihydroindenopyridines, regioisomers, Michael additionАннотация
The ratio of dihydroindenopyridine regioisomers formed from ethyl β-amino-crotonate and 4- or 5-monosubstituted 2-arylideneindane-1,3-dione depends on total electronic and steric effects of the indanedione substituents.
How to Cite
Muceniece, D.; Popelis, J.; Lūsis, V. Chem. Heterocycl. Compd. 2008, 44, 35. [Khim. Geterotsikl. Soedin. 2008, 42.]
For this article in the English edition see DOI 10.1007/s10593-008-0014-8
