Indoloquinolines, indolobenzoxazines and quinazolophthalazines prepared from norbornane/eneamino acids and hydrazides

Géza Stájer, Angela E. Szabó, György Túrós, Pál Sohár, Reijo Sillanpää

Research output: Article

3 Citations (Scopus)

Abstract

The reactions of di-endo- and di-exo-aminonorbornane/enecarboxylic acids 1-4 with ethyl 2-(2-oxocyclohexyl)acetate afforded methanoindoloquinolines 5, 6, 8, and 9, the oxo ester participating as a two-membered sp2 building block. In the cases of di-exo- and di-endo-aminonorbornenecarboxylic acids 2 and 4, methanoindolobenzoxazinediones 7 and 10 were also formed; compound 7 was also isolated from the mother liquor of 10. The reactions of ethyl 2-(2-oxocyclohexyl)acetate with aminonorbornane/enecarbohydrazides 11-14 result in the methanoquinazolophthalazines 15-18. The structures of the compounds were elucidated by NMR spectroscopy, and for 6, 7, 8, and 10 also by X-ray crystallography.

Original languageEnglish
Pages (from-to)4154-4161
Number of pages8
JournalEuropean Journal of Organic Chemistry
Issue number19
DOIs
Publication statusPublished - szept. 26 2005

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ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry

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