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0001625508
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The Pictet-Spengler Synthesis of Tetrahydroisoquinolines and Related Compounds
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Adams R. (Ed), John Wiley and Sons, New York, USA
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Whaley W.M., and Govindachari T.R. The Pictet-Spengler Synthesis of Tetrahydroisoquinolines and Related Compounds. In: Adams R. (Ed). Organic Reactions 6 (1951), John Wiley and Sons, New York, USA 151
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Whaley, W.M.1
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0000235287
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Katritzky A.R., and Rees C.W. (Eds), Pergamon, Oxford, UK
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Jones G. In: Katritzky A.R., and Rees C.W. (Eds). Comprehensive Heterocyclic Chemistry Vol. 2 (1984), Pergamon, Oxford, UK 438-440
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Jones, G.1
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6
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27544453677
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Synthesis of Optically-Active Isoquinoline and Indole Alkaloids Employing the Pictet-Spengler Condensation with Removable Chiral Auxiliaries Bound to Nitrogen
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Vicario J.L. (Ed), Research SignPost, Trivandrum Chapter 4
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Kaufman T.S. Synthesis of Optically-Active Isoquinoline and Indole Alkaloids Employing the Pictet-Spengler Condensation with Removable Chiral Auxiliaries Bound to Nitrogen. In: Vicario J.L. (Ed). New Methods for the Asymmetric Synthesis of Nitrogen Heterocycles (2005), Research SignPost, Trivandrum 99-147 Chapter 4
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0012566719
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Use of Carbonyl Derivatives for Heterocyclic Synthesis
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Winterfeldt E. (Ed), Pergamon Press, Oxford, UK
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Bringmann G., Ewers C.L.J., and Walter R. Use of Carbonyl Derivatives for Heterocyclic Synthesis. In: Winterfeldt E. (Ed). Comprehensive Organic Synthesis Vol. 6 (1991), Pergamon Press, Oxford, UK 736-740
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Kubo A., Saito N., Kawakami N., Matsuyama Y., and Miwa T. Synthesis (1987) 824
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Miwa, T.5
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85064266610
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Cheung G.K., Earle M.J., Fairhurst R.A., Heaney H., Shihaibar K.F., Eyley S.C., and Ince F. Synlett (1991) 721
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Cheung, G.K.1
Earle, M.J.2
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Heaney, H.4
Shihaibar, K.F.5
Eyley, S.C.6
Ince, F.7
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29
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33748746277
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note
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4), concentrated under reduced pressure, and the residue was submitted to column chromatography.
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30
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33748746626
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note
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4S requires C, 57.37; H, 4.81; N, 2.79.
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33
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4544387854
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Koepler O., Laschat S., Baro A., Fischer P., Miehlich B., Hotfilder M., and le Viseur C. Eur. J. Org. Chem. (2004) 3611
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Koepler, O.1
Laschat, S.2
Baro, A.3
Fischer, P.4
Miehlich, B.5
Hotfilder, M.6
le Viseur, C.7
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34
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0033978692
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Thioacetals have been employed for the synthesis of tetrahydroisoquinoline derivatives, via thionium ions, see:
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Thioacetals have been employed for the synthesis of tetrahydroisoquinoline derivatives, via thionium ions, see:. Padwa A., and Waterson A.G. J. Org. Chem. 65 (2000) 235
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J. Org. Chem.
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Padwa, A.1
Waterson, A.G.2
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