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| 005 | 20250317134725.0 | ||
| 008 | 250317b |||||||| |||| 00| 0 eng d | ||
| 022 | _a09743626 | ||
| 040 |
_aMSU _bEnglish _cMSU _erda |
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| 050 | 0 | 0 | _aQD31 JOU |
| 100 | 1 |
_aMangalaraj, S. _eauthor |
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| 245 | 1 | 0 |
_aSyntheses of fused tetrahydro-β-carboline analogues through imide carbonyl activation using BBr3 : _bevidence for the involvement of fused cyclic N-acyliminium ion intermediate / _ccreated by S. Mangalaraj, J. Selvakumar and C. Ramanathan |
| 264 | 1 |
_aBangalore : _bSpringer, _c2015. |
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| 336 |
_2rdacontent _atext _btxt |
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| 337 |
_2rdamedia _aunmediated _bn |
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| 338 |
_2rdacarrier _avolume _bnc |
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| 440 |
_aJournal of chemical sciences _vVolume 127, number 5, |
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| 520 | 3 | _aThe 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. | |
| 650 |
_aIntramolecular cyclization _vFused cyclic N-acyliminium ion _xTetrahydro-β-carboline |
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| 700 | 1 |
_aSelvakumar, J _eco author |
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| 700 | 1 |
_aRamanathan, C. _eco author |
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| 856 | _uhttps://doi.org/10.1007/s12039-015-0836-8 | ||
| 942 |
_2lcc _cJA |
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| 999 |
_c169314 _d169314 |
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