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0033929179
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Since 1995 the new chemistry of multicomponent reactions and their libraries, including their heterocyclic chemistry
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Ugi, I.1
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0034665244
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Maximizing synthetic efficiency: Multi-component reactions lead the way
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(b) Bienaymé, H., Hulme, C., Oddon, G. and Schmitt, P., Maximizing synthetic efficiency: multi-component reactions lead the way, Chem. Eur. J., 6 (2000) 3321-3329.
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Bienaymé, H.1
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Oddon, G.3
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3
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0035030563
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The multicomponent reactions and their libraries for natural and preparative chemistry
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(c) Ugi, I. and Heck, S., The multicomponent reactions and their libraries for natural and preparative chemistry, Comb. Chem. High Throughput Screening, 4 (2001) 1-34.
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Comb. Chem. High Throughput Screening
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Ugi, I.1
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Pharmacophore features of potential drugs
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Muegge, I.1
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Medicinal chemistry: Challenges and opportunities
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Wess, G.1
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0036025610
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Rapid analogue synthesis of heteroaromatic compounds
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(c) Collins, I., Rapid analogue synthesis of heteroaromatic compounds, J. Chem. Soc., Perkin Trans. 1, (2002) 1921-1940.
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Collins, I.1
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7
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0001595120
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Role reversal in the cyclocondensation of cyclopentadiene with heterodienophiles derived from arylamines and aldehydes: Synthesis of novel tetrahydroquinolines
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(a) Grieco, P. and Bahsas, A., Role reversal in the cyclocondensation of cyclopentadiene with heterodienophiles derived from arylamines and aldehydes: synthesis of novel tetrahydroquinolines, Tetrahedron Lett., 29 (1988) 5855-5858.
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Grieco, P.1
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Lanthanide triflate catalyzed imino Diels-Alder reactions; convenient synthesis of pyridine and quinoline derivatives
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(b) Kobayashi, S., Ishitani, H. and Nagayama, S., Lanthanide triflate catalyzed imino Diels-Alder reactions; convenient synthesis of pyridine and quinoline derivatives, Synthesis, (1995) 1195-1202.
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Kobayashi, S.1
Ishitani, H.2
Nagayama, S.3
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10
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0032770704
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Scandium triflate in organic synthesis
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(a) Kobayashi, S. Scandium triflate in organic synthesis, Eur. J. Org. Chem., (1999) 15-27.
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Kobayashi, S.1
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0036105107
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Development of novel Lewis acid catalysts for selective organic reactions in aqueous media
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(b) Kobayashi, S. and Manabe, K., Development of novel Lewis acid catalysts for selective organic reactions in aqueous media, Acc. Chem. Res., 35 (2002) 209-217.
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Kobayashi, S.1
Manabe, K.2
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Lewis acid. A new type of polymer-supported Lewis acid catalyst of wide utility in organic synthesis
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(c) Kobayashi, S. and Nagayama, S., A microencapsulated Lewis acid. A new type of polymer-supported Lewis acid catalyst of wide utility in organic synthesis, J. Am. Chem. Soc., 120 (1998) 2985-2986.
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Kobayashi, S.1
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Microencapsulated, A.3
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0036459071
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Scandium triflate immobilized in ionic liquids: A novel and recyclable catalytic system for hetero-Diels-Alder reactions
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(d) Yadav, J. S., Reddy, B. V. S., Uma Gayathri, K. and Prasad, A. R., Scandium triflate immobilized in ionic liquids: a novel and recyclable catalytic system for hetero-Diels-Alder reactions, Synthesis, (2002) 2537-2541.
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Yadav, J.S.1
Reddy, B.V.S.2
Uma Gayathri, K.3
Prasad, A.R.4
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14
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0037529208
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Dihydropyridine-based multicomponent reactions. Efficient entry into new tetrahydroquinoline systems through Lewis acid-catalyzed formal [4 + 2] cycloadditions
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Lavilla, R., Bernabeu, M. C., Carranco, I. and Díaz, J. L., Dihydropyridine-based multicomponent reactions. Efficient entry into new tetrahydroquinoline systems through Lewis acid-catalyzed formal [4 + 2] cycloadditions, Org. Lett., 5 (2003) 717-720.
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Lavilla, R.1
Bernabeu, M.C.2
Carranco, I.3
Díaz, J.L.4
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15
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0037170892
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Indium trichloride catalyzed one-step synthesis of α-amino nitriles by a three-component condensation of carbonyl compounds, amines and potassium cyanide
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For well documented representative examples, see: (a) Ranu, B. C., Dey, S. S. and Hajra, A., Indium trichloride catalyzed one-step synthesis of α-amino nitriles by a three-component condensation of carbonyl compounds, amines and potassium cyanide, Tetrahedron, 58 (2002) 2529-2532.
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Ranu, B.C.1
Dey, S.S.2
Hajra, A.3
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16
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0001641346
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General procedure for the synthesis of α-amino phosphonates from aldehydes and ketones using indium (111) chloride as a catalyst
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(b) Ranu, B. C., Hajra, A. and Jana, U., General procedure for the synthesis of α-amino phosphonates from aldehydes and ketones using indium (111) chloride as a catalyst, Org. Lett., 1 (1999) 1141-1143.
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Ranu, B.C.1
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Jana, U.3
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0343056648
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Reaction of N-alkylheteroaromatic cation with phosphite
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Takeuchi, I., Shibata, Y. and Hamada, Y., Reaction of N-alkylheteroaromatic cation with phosphite, Heterocycles, 23 (1985) 1635-1638.
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Takeuchi, I.1
Shibata, Y.2
Hamada, Y.3
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18
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0025916281
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Regioselective synthesis of indolydihydropyridines. A remarkable solvent effect
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(a) For the regioselective formation of 4-indolyl-1,4-DHPs, see: Lavilla, R., Gotsens, T. and Bosch, J., Regioselective synthesis of indolydihydropyridines. A remarkable solvent effect, Synthesis (1991) 842-844.
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Synthesis
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Lavilla, R.1
Gotsens, T.2
Bosch, J.3
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19
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0343607421
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Competitive addition of carbon, sulfur, and nitrogen nucleophiles to quaternized heteroaromatic compounds in liquid ammonia
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(b) For the regioselective formation of 4-sulfanyl-1,4-DHPs, see: Zoltewicz, J. A., Helmick, L. S. and O'Halloran, J. K., Competitive addition of carbon, sulfur, and nitrogen nucleophiles to quaternized heteroaromatic compounds in liquid ammonia, J. Org. Chem., 41 (1976) 1308-1313.
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Zoltewicz, J.A.1
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O'Halloran, J.K.3
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20
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0037420992
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Addition of some heterocycles to N-benzyl-3-cyanopyridinium chloride
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Volochnyuk, D. M., Kostuyk, A. N., Pinchuk, A. M. and Tolmachev, A. A., Addition of some heterocycles to N-benzyl-3-cyanopyridinium chloride, Tetrahedron Lett., 44 (2003) 391-394.
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21
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0034829773
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Catalytic enantioselective Reissert-type reaction: Development and application to the synthesis of a potent NMDA receptor antagonist (-)-L-689,560 using a solid-supported catalyst
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and references cited therein
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Takamura, M., Funabashi, K., Kanai and Shibasaki, M., Catalytic enantioselective Reissert-type reaction: development and application to the synthesis of a potent NMDA receptor antagonist (-)-L-689,560 using a solid-supported catalyst, J. Am. Chem. Soc., 123 (2001) 6801-6808, and references cited therein.
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Takamura, M.1
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Kanai3
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22
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0037433983
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A tandem Petasis-Ugi multi component condensation reaction: Solution phase synthesis of six dimensional libraries
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For a tandem transformation linking two 3CRs, see: (a) Portlock, D. E., Ostaszewski, R., Naskar, D. and West, L., A tandem Petasis-Ugi multi component condensation reaction: solution phase synthesis of six dimensional libraries, Tetrahedron Lett., 44 (2003) 603-605.
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Portlock, D.E.1
Ostaszewski, R.2
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0035796515
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Repetitive Ugi reactions
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(b) Constabel, F. and Ugi, I., Repetitive Ugi reactions, Tetrahedron, 57 (2001) 5785-5789.
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