4a-ALKYL DERIVATIVES OF 5-OXO-4H-4a,5-DIHYDROINDENO[1,2-<i>b</i>]PYRIDINE

Authors

  • Д. Муцениеце Latvian Institute of Organic Synthesis, Riga LV-1006
  • С. Ступникова Latvian Institute of Organic Synthesis, Riga LV-1006
  • В. Лусис Latvian Institute of Organic Synthesis, Riga LV-1006

Keywords:

dihydroindeno[1,2-b]pyridines, alkylation

Abstract

High selectivity has been discovered for the C-alkylation of ambident anions of 5-oxo-1H-4,5-dihydroindeno[1,2-b]pyridines with ethyl bromoacetate, allyl, propargyl, and phenacyl bromides, which leads to the formation of the corresponding 4a-substituted 5-oxo-4H-4a,5-dihydroindeno[1,2-b]pyridines in high yield.

How to Cite
Muceniece, D.; Stupnikova, S.; Lusis, V. Chem. Heterocycl. Compd. 2001, 37, 982. [Khim. Geterotsikl. Soedin. 2001, 1071.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1012787517710

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Published

2001-08-25

Issue

No. 8 (2001)

Section

Original Papers