Syntheses of fused tetrahydro-β-carboline analogues through imide carbonyl activation using BBr3 : evidence for the involvement of fused cyclic N-acyliminium ion intermediate /
Mangalaraj, S.
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 - Journal of chemical sciences Volume 127, number 5, .
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.
09743626
Intramolecular cyclization--Tetrahydro-β-carboline--Fused cyclic N-acyliminium ion
QD31 JOU
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 - Journal of chemical sciences Volume 127, number 5, .
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.
09743626
Intramolecular cyclization--Tetrahydro-β-carboline--Fused cyclic N-acyliminium ion
QD31 JOU