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2000
Volume 17, Issue 17
  • ISSN: 1385-2728
  • E-ISSN: 1875-5348

Abstract

The Staudinger reaction of various β-carboline derivatives with aryloxyacetyl chlorides led to novel fused tetracyclic compounds containing two biologically considerable cores, such as the β-carboline and the β-lactam units. The reaction is stereoselective, giving exclusively the cis cycloadducts as racemates. The mechanism and the 100% stereoselectivity of this cycloaddition was studied by high level quantum chemical calculations.

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/content/journals/coc/10.2174/13852728113179990035
2013-09-01
2025-08-13
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/content/journals/coc/10.2174/13852728113179990035
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  • Article Type:
    Research Article
Keyword(s): Cycloaddition; Mechanism; Staudinger reaction; β-Carbolines; β-Lactams
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