SYNTHESIS AND REACTIONS OF METHYL 8-ARYL-6-METHYL-9-OXO-8,9-DIHYDRO-5<i>H</i>-DIBENZO[4,5:6,7]CYCLOHEPTA[1,2-<i>b</i>]PYRIDINE-7-CARBOXYLATES

Авторы

  • O. Kodolins Latvian Institute of Organic Synthesis
  • V. Lusis Latvian Institute of Organic Synthesis
  • D. Muceniece Latvian Institute of Organic Synthesis

DOI:

https://doi.org/10.1007/1750

Ключевые слова:

6-arylidenedibenzo[a, c][7]annulene-5, 7(6H)-diones, dibenzo[4, 5, 6, 7]cyclohepta[1, 2-b]pyridine, diphenic anhydride, fused 1, 4-dihydropyridines

Аннотация

A method for the synthesis of methyl 4-aryl-6-methyl-9-oxo-8,9-dihydro-5H-dibenzo[4,5:6,7]cyclohepta[1,2-b]pyridine-7-carboxylates from 6-arylidenedibenzo[a,c][7]annulene-5,7(6H)-diones and methyl 3-aminocrotonate has been developed. The alkylation, oxidation, and reduction of the obtained annulated dihydropyridines were studied.

How to Cite
Kodolins, O.; Lusis, V.; Muceniece, D. Chem. Heterocycl. Compd. 2014, 50, 1270. [Khim. Geterotsikl. Soedin. 2014, 1378.]

For this article in the English edition see DOI 10.1007/s10593-014-1589-x

Биографии авторов

O. Kodolins, Latvian Institute of Organic Synthesis

Oskars Kodolins

V. Lusis, Latvian Institute of Organic Synthesis

Viesturs Lūsis

D. Muceniece, Latvian Institute of Organic Synthesis

Dzintra Muceniece

Загрузки

Опубликован

2014-09-30

Выпуск

№ 9 (2014)

Раздел

Оригинальные статьи