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Gaillard S., Papamicaël C., Marsais F., Dupas G., and Levacher V. Synlett (2005) 441
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Gaillard, S.1
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11
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0029856245
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For an example of synthesis of N-benzyl 1,4-dihydropyridine from 1-aza-1,3-butadiene via a Diels-Alder reaction, see:
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For an example of synthesis of N-benzyl 1,4-dihydropyridine from 1-aza-1,3-butadiene via a Diels-Alder reaction, see:. Geirsson J.K.F., and Johannesdottir J.F. J. Org. Chem. 61 (1996) 7320
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1242306175
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For an example, see:
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For an example, see:. Volochnyuk D.M., Kostyuk A.N., Sibgatulin D.A., Chernega A.N., Pinchuk A.M., and Tolmachev A.A. Tetrahedron 60 (2004) 2361
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Volochnyuk, D.M.1
Kostyuk, A.N.2
Sibgatulin, D.A.3
Chernega, A.N.4
Pinchuk, A.M.5
Tolmachev, A.A.6
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14
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9744257740
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For a recent discussion on tandem, cascade and one pot reactions, see:
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For a recent discussion on tandem, cascade and one pot reactions, see:. Fogg D.E., and dos Santos E.N. Coord. Chem. Rev. 248 (2004) 2365
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dos Santos, E.N.2
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Bolm C., Rantanen T., Schiffers I., and Zani L. Angew. Chem., Int. Ed. 44 (2005) 1758
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Bolm, C.1
Rantanen, T.2
Schiffers, I.3
Zani, L.4
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22
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33845205051
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For the first enantioselective Biginelli reaction catalyzed by chiral phosphoric acid, see:
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For the first enantioselective Biginelli reaction catalyzed by chiral phosphoric acid, see:. Chen X.-H., Xu X.-Y., Liu H., Cun L.-F., and Gong L.-Z. J. Am. Chem. Soc. 128 (2006) 14802
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Gong, L.-Z.5
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23
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26844487901
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For the use of polyphosphates for the Biginelli reaction:
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For the use of polyphosphates for the Biginelli reaction:. Kappe C.O., and Falsone F.S. Synlett (1998) 718
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(1998)
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Kappe, C.O.1
Falsone, F.S.2
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4344709593
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Van der Vlugt J.I., Hewat A.C., Neto S., Sablong R., Mills A.M., Lutz M., Spek A.L., Müller C., and Vogt D. Adv. Synth. Catal. 346 (2004) 993
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Mills, A.M.5
Lutz, M.6
Spek, A.L.7
Müller, C.8
Vogt, D.9
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27
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33750154643
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For the synthesis of Hantzsch type dihydropyridines assisted by PTSA using high-temperature water and microwave heating, see:
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For the synthesis of Hantzsch type dihydropyridines assisted by PTSA using high-temperature water and microwave heating, see:. Tu S.-J., Jiang B., Zhang J.-Y., Jia R.-H., Zhang Y., and Yao C.-S. Org. Biomol. Chem. 4 (2006) 3980
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Tu, S.-J.1
Jiang, B.2
Zhang, J.-Y.3
Jia, R.-H.4
Zhang, Y.5
Yao, C.-S.6
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29
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35848937807
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note
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Enantiomeric excesses were determined by HPLC analysis after purification: Daicel Chiralcel OD-H, i-PrOH/hexane = 3:97, UV: 254 nm, flow rate: 0.8 ml/min.
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30
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0037043058
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For an asymmetric synthesis of 1,4-dihydropyridines via diastereoselective approaches, see:
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For an asymmetric synthesis of 1,4-dihydropyridines via diastereoselective approaches, see:. Ashworth I., Hopes P., Levin D., Patel I., and Salloo R. Tetrahedron Lett. 43 (2002) 4931
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(2002)
Tetrahedron Lett.
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Ashworth, I.1
Hopes, P.2
Levin, D.3
Patel, I.4
Salloo, R.5
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