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Syntheses of fused tetrahydro-β-carboline analogues through imide carbonyl activation using BBr3 : evidence for the involvement of fused cyclic N-acyliminium ion intermediate / created by S. Mangalaraj, J. Selvakumar and C. Ramanathan

By: Contributor(s): Material type: TextTextSeries: Journal of chemical sciences ; Volume 127, number 5,Bangalore : Springer, 2015Content type:
  • text
Media type:
  • unmediated
Carrier type:
  • volume
ISSN:
  • 09743626
Subject(s): LOC classification:
  • QD31 JOU
Online resources: Abstract: The fused cyclic N-acyliminium ion generated during the imide carbonyl activation reaction of phenethylphthalimide was confirmed by single crystal X-ray diffraction. The Lewis acid assisted imide carbonyl activation methodology was successfully extended to synthesize fused tetrahydro-β-carboline units from the corresponding N-indolylethylimides.
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Item type Current library Call number Vol info Status Notes Date due Barcode
Journal Article Journal Article Main Library - Special Collections QD31 JOU (Browse shelf(Opens below)) Vol. 127, no.5 (pages 811-819) Not for loan For in house use only

The fused cyclic N-acyliminium ion generated during the imide carbonyl activation reaction of phenethylphthalimide was confirmed by single crystal X-ray diffraction. The Lewis acid assisted imide carbonyl activation methodology was successfully extended to synthesize fused tetrahydro-β-carboline units from the corresponding N-indolylethylimides.

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