Approaches to the formation of condensed isoindolones

Ferenc Csende, G. Stájer

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

The development of novel synthetic methods for the preparation of condensed aromatic and saturated isoindolones containing one or more heteroatoms is described and several new types of related ring systems are presented. The frequently applied N-acyliminium ion cyclization, the cyclocondensation of dicarbonyl compounds (e,g. γ-oxoacids) with amines and the photoinduced intramolecular ring-closure of N-substituted phthalimides are utilized in the syntheses. The enantioselective and diastereoselective procedures with the ratios of the isomers obtained are also discussed.

Original languageEnglish
Pages (from-to)1261-1276
Number of pages16
JournalCurrent Organic Chemistry
Volume9
Issue number13
DOIs
Publication statusPublished - Sep 2005

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Phthalimides
Keto Acids
Cyclization
Isomers
Amines
Ions
Isoindol-1-one

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Approaches to the formation of condensed isoindolones. / Csende, Ferenc; Stájer, G.

In: Current Organic Chemistry, Vol. 9, No. 13, 09.2005, p. 1261-1276.

Research output: Contribution to journalArticle

Csende, Ferenc ; Stájer, G. / Approaches to the formation of condensed isoindolones. In: Current Organic Chemistry. 2005 ; Vol. 9, No. 13. pp. 1261-1276.
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