-
1
-
-
0000354729
-
α,β-Unsaturated ethers and their analogues in reactions of diene synthesis
-
Povarov, L. S. α,β-Unsaturated ethers and their analogues in reactions of diene synthesis. Russ. Chem. Rev., 1967, 36, 656-670.
-
(1967)
Russ. Chem. Rev.
, vol.36
, pp. 656-670
-
-
Povarov, L.S.1
-
4
-
-
0141922087
-
Dihydropyridine-based MCRs. New reaction pathways in the interaction with ethyl glyoxalate and non-aromatic amines
-
Carranco, I.; Diaz, J. L.; Jiménez, O.; Lavilla, R. Dihydropyridine-based MCRs. New reaction pathways in the interaction with ethyl glyoxalate and non-aromatic amines. Tetrahedron Lett., 2003, 44, 8449-8452.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 8449-8452
-
-
Carranco, I.1
Diaz, J.L.2
Jiménez, O.3
Lavilla, R.4
-
5
-
-
37049081690
-
Acid-catalysed addition of N-aryl imines to dihydrofuran. Postulated dependence of the reaction mechanism on the relative face of approach of reactants
-
Lucchini, V.; Prato, M.; Scorrano, G.; Stivanello, M.; Valle, G. Acid-catalysed addition of N-aryl imines to dihydrofuran. Postulated dependence of the reaction mechanism on the relative face of approach of reactants. J. Chem. Soc. Perkin Trans., 1992, 2, 259-266.
-
(1992)
J. Chem. Soc. Perkin Trans.
, vol.2
, pp. 259-266
-
-
Lucchini, V.1
Prato, M.2
Scorrano, G.3
Stivanello, M.4
Valle, G.5
-
6
-
-
0035898269
-
Recent developments in imino Diels-Alder reactions
-
Buonora, P.; Olsen, J.-C.; Oh, T. Recent developments in imino Diels-Alder reactions. Tetrahedron, 2001, 57, 6099-6138.
-
(2001)
Tetrahedron
, vol.57
, pp. 6099-6138
-
-
Buonora, P.1
Olsen, J.-C.2
Oh, T.3
-
7
-
-
4744364091
-
Mechanistic studies on the formal aza-Diels-Alder reactions of N-aryl imines: evidence for the non-concertedness under Lewis-acid catalysed conditions
-
Hermitage, S.; Howard, J. A. K.; Jay, D.; Pritchard, R. G.; Probert, M. R.; Whiting, A. Mechanistic studies on the formal aza-Diels-Alder reactions of N-aryl imines: evidence for the non-concertedness under Lewis-acid catalysed conditions. Org. Biomol. Chem., 2004, 2, 2451-2460.
-
(2004)
Org. Biomol. Chem.
, vol.2
, pp. 2451-2460
-
-
Hermitage, S.1
Howard, J.A.K.2
Jay, D.3
Pritchard, R.G.4
Probert, M.R.5
Whiting, A.6
-
9
-
-
0034952519
-
Clay/water mixtures - a heterogeneous and ecologically efficient catalyst for the three-component stereoselective synthesis of tetrahydroquinolines
-
Sartori, G.; Bigi, F.; Maggi, R.; Mazzacani, A.; Oppici, G. Clay/water mixtures - a heterogeneous and ecologically efficient catalyst for the three-component stereoselective synthesis of tetrahydroquinolines. Eur. J. Org. Chem., 2001, 2513-2518.
-
(2001)
Eur. J. Org. Chem.
, pp. 2513-2518
-
-
Sartori, G.1
Bigi, F.2
Maggi, R.3
Mazzacani, A.4
Oppici, G.5
-
10
-
-
0000128579
-
2O catalyzed [4+2] cycloaddition reactions of N-aryl Schiff's bases with 1-alkenyl, 1,2-propadienyl, and 1-alkynyl sulfides
-
2O catalyzed [4+2] cycloaddition reactions of N-aryl Schiff's bases with 1-alkenyl, 1,2-propadienyl, and 1-alkynyl sulfides. Heterocycles, 1993, 35, 1039-1053.
-
(1993)
Heterocycles
, vol.35
, pp. 1039-1053
-
-
Narasaka, K.1
Shibata, T.2
-
11
-
-
0029135125
-
Lanthanide triflate catalyzed imino diels-alder reactions; convenient syntheses of pyridine and quinoline derivatives
-
Kobayashi, S.; Ishitani, H.; Nagayama, S. Lanthanide triflate catalyzed imino diels-alder reactions; convenient syntheses of pyridine and quinoline derivatives. Synthesis, 1995, 1195-1202.
-
(1995)
Synthesis
, pp. 1195-1202
-
-
Kobayashi, S.1
Ishitani, H.2
Nagayama, S.3
-
13
-
-
61349084177
-
Recent synthetic developments in a powerful imino Diels-Alder reaction (Povarov reaction): application to the synthesis of N-polyheterocycles and related alkaloids
-
Kouznetsov, V. V. Recent synthetic developments in a powerful imino Diels-Alder reaction (Povarov reaction): application to the synthesis of N-polyheterocycles and related alkaloids. Tetrahedron, 2009, 65, 2721-2750.
-
(2009)
Tetrahedron
, vol.65
, pp. 2721-2750
-
-
Kouznetsov, V.V.1
-
14
-
-
43949108252
-
Synthesis of substituted 1,2,3,4-tetrahydroquinolines by the povarov reaction. new potentials of the classical reaction
-
Glushkov, V. A.; Tolstikov, A. G. Synthesis of substituted 1,2,3,4-tetrahydroquinolines by the povarov reaction. new potentials of the classical reaction. Russ. Chem. Rev., 2008, 77, 137-159.
-
(2008)
Russ. Chem. Rev.
, vol.77
, pp. 137-159
-
-
Glushkov, V.A.1
Tolstikov, A.G.2
-
15
-
-
0037529208
-
Dihydropyridine-based multicomponent reactions. efficient entry into new tetrahydroquinoline systems through lewis acid-catalyzed formal [4 + 2] cycloadditions
-
Lavilla, R.; Bernabeu, M. C.; Carranco, I.; Díaz, J. L. Dihydropyridine-based multicomponent reactions. efficient entry into new tetrahydroquinoline systems through lewis acid-catalyzed formal [4 + 2] cycloadditions. Org. Lett., 2003, 5, 717-720.
-
(2003)
Org. Lett.
, vol.5
, pp. 717-720
-
-
Lavilla, R.1
Bernabeu, M.C.2
Carranco, I.3
Díaz, J.L.4
-
16
-
-
0036012737
-
Recent developments in the chemistry of dihydropyridines
-
Lavilla, R. Recent developments in the chemistry of dihydropyridines. J. Chem. Soc. Perkin Trans., 2002, 1, 1141-1156.
-
(2002)
J. Chem. Soc. Perkin Trans.
, vol.1
, pp. 1141-1156
-
-
Lavilla, R.1
-
17
-
-
2342429191
-
Non-conventional redox chemistry of dihydropyridines and pyridinium salts
-
Lavilla, R. Non-conventional redox chemistry of dihydropyridines and pyridinium salts. Curr. Org. Chem., 2004, 8, 715-737.
-
(2004)
Curr. Org. Chem.
, vol.8
, pp. 715-737
-
-
Lavilla, R.1
-
18
-
-
13544253604
-
Multicomponent reactions with dihydroazines: efficient synthesis of a diverse set of pyrido-fused tetrahydroquinolines
-
Carranco, I.; Díaz, J. L.; Jiménez, O.; Vendrell, M.; Albericio, F.; Royo, M.; Lavilla, R. Multicomponent reactions with dihydroazines: efficient synthesis of a diverse set of pyrido-fused tetrahydroquinolines. J. Comb. Chem., 2005, 7, 33-41.
-
(2005)
J. Comb. Chem.
, vol.7
, pp. 33-41
-
-
Carranco, I.1
Díaz, J.L.2
Jiménez, O.3
Vendrell, M.4
Albericio, F.5
Royo, M.6
Lavilla, R.7
-
19
-
-
0035944441
-
Metal ion-catalyzed cycloaddition vs hydride transfer reactions of NADH analogues with p-Benzoquinones
-
Fukuzumi, S.; Fujii, Y.; Suenobu, T. Metal ion-catalyzed cycloaddition vs hydride transfer reactions of NADH analogues with p-Benzoquinones. J. Am. Chem. Soc., 2001, 123, 10191-10199.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 10191-10199
-
-
Fukuzumi, S.1
Fujii, Y.2
Suenobu, T.3
-
20
-
-
0037156431
-
Reductive amination of aldehydes and ketones by a Hantzsch dihydropyridine using scandium triflate as a catalyst
-
Itoh, T.; Nagata, K.; Kurihara, A.; Miyazaki, M.; Ohsawa, A. Reductive amination of aldehydes and ketones by a Hantzsch dihydropyridine using scandium triflate as a catalyst. Tetrahedron Lett., 2002, 43, 3105-3108.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 3105-3108
-
-
Itoh, T.1
Nagata, K.2
Kurihara, A.3
Miyazaki, M.4
Ohsawa, A.5
-
21
-
-
4143066159
-
A selective reductive amination of aldehydes by the use of Hantzsch dihy-dropyridines as reductant
-
Itoh, T.; Nagata, K.; Miyazaki, M.; Ishikawa, H.; Kurihara, A.; Ohsawa, A. A selective reductive amination of aldehydes by the use of Hantzsch dihy-dropyridines as reductant. Tetrahedron, 2004, 60, 6649-6655.
-
(2004)
Tetrahedron
, vol.60
, pp. 6649-6655
-
-
Itoh, T.1
Nagata, K.2
Miyazaki, M.3
Ishikawa, H.4
Kurihara, A.5
Ohsawa, A.6
-
22
-
-
17844396460
-
1,4-Dihydropicolinic acid derivatives: novel NADH analogues with an altered connectivity pattern
-
Gómez, E.; Miguel, M.; Jiménez, O.; de la Rosa, G.; Lavilla, R. 1,4-Dihydropicolinic acid derivatives: novel NADH analogues with an altered connectivity pattern. Tetrahedron Lett., 2005, 46, 3513-3516.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 3513-3516
-
-
Gómez, E.1
Miguel, M.2
Jiménez, O.3
de la Rosa, G.4
Lavilla, R.5
-
23
-
-
53049106528
-
Auto-tandem catalysis in the synthesis of substituted quinolines from aldimines and electron-rich olefins: cascade povarov-hydrogen-transfer reaction
-
Shindoh, N.; Tokuyama, H.; Takemoto, Y.; Takasu, K. Auto-tandem catalysis in the synthesis of substituted quinolines from aldimines and electron-rich olefins: cascade povarov-hydrogen-transfer reaction. J. Org. Chem., 2008, 73, 7451-7456.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 7451-7456
-
-
Shindoh, N.1
Tokuyama, H.2
Takemoto, Y.3
Takasu, K.4
-
24
-
-
34250895534
-
Ethynyl ketene-S,S-acetals: the highly reactive electron-rich dienophiles and applications in the synthesis of 4-functionalized quinolines via a one-pot three-component reaction
-
Zhao, Y.-L.; Zhang, W.; Wang, S.; Liu, Q. Ethynyl ketene-S,S-acetals: the highly reactive electron-rich dienophiles and applications in the synthesis of 4-functionalized quinolines via a one-pot three-component reaction. J. Org. Chem., 2007, 72, 4985-4988.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 4985-4988
-
-
Zhao, Y.-L.1
Zhang, W.2
Wang, S.3
Liu, Q.4
-
25
-
-
78650001613
-
Synthesis and cycloaddition reactions of ethyl glyoxylate imines. Synthesis of substituted furo-[3,2-c]quinolines and 7H-indeno[2,1-c]quinolines
-
Borrione, E.; Prato, M.; Scorrano, G.; Stivanello, M.; Lucchini, V. Synthesis and cycloaddition reactions of ethyl glyoxylate imines. Synthesis of substituted furo-[3,2-c]quinolines and 7H-indeno[2,1-c]quinolines. J. Heterocycl. Chem., 1988, 25, 1831-1835.
-
(1988)
J. Heterocycl. Chem.
, vol.25
, pp. 1831-1835
-
-
Borrione, E.1
Prato, M.2
Scorrano, G.3
Stivanello, M.4
Lucchini, V.5
-
26
-
-
30744468567
-
An efficient synthesis of new C-2 aryl substituted quinolines based on three component imino Diels-Alder reaction
-
Kouznetsov, V. V.; Bohórquez, A.; Saavedra, L.; Medina, R. An efficient synthesis of new C-2 aryl substituted quinolines based on three component imino Diels-Alder reaction. Mol. Divers., 2006, 10, 29-37.
-
(2006)
Mol. Divers.
, vol.10
, pp. 29-37
-
-
Kouznetsov, V.V.1
Bohórquez, A.2
Saavedra, L.3
Medina, R.4
-
27
-
-
33646033447
-
An efficient one-pot synthesis of tetrahydroquinoline derivatives via an aza Diels-Alder reaction mediated by CAN in an aqueous medium and oxidation to heteroaryl quinolines
-
Savitha, G.; Perumal, P. T. An efficient one-pot synthesis of tetrahydroquinoline derivatives via an aza Diels-Alder reaction mediated by CAN in an aqueous medium and oxidation to heteroaryl quinolines. Tetrahedron Lett., 2006, 47, 3589-3593.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 3589-3593
-
-
Savitha, G.1
Perumal, P.T.2
-
28
-
-
59249101684
-
Convenient, two-step synthesis of 2-styrylquinolines: an application of the CAN-catalyzed vinylogous type-II Povarov reaction
-
Sridharan, V.; Avendaño, C.; Menéndez, J. C. Convenient, two-step synthesis of 2-styrylquinolines: an application of the CAN-catalyzed vinylogous type-II Povarov reaction. Tetrahedron, 2009, 65, 2087-2096.
-
(2009)
Tetrahedron
, vol.65
, pp. 2087-2096
-
-
Sridharan, V.1
Avendaño, C.2
Menéndez, J.C.3
-
29
-
-
33646022857
-
A CAN-initiated aza-Diels-Alder reaction for a facile synthesis of 4-amido-N-yl tetrahydroquinolines
-
Han, B.; Jia, X.-D.; Jin, X.-L.; Zhou, Y.-L.; Yang, L.; Liu, Z.-L.; Yu, W. A CAN-initiated aza-Diels-Alder reaction for a facile synthesis of 4-amido-N-yl tetrahydroquinolines. Tetrahedron Lett., 2006, 47, 3545-3547.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 3545-3547
-
-
Han, B.1
Jia, X.-D.2
Jin, X.-L.3
Zhou, Y.-L.4
Yang, L.5
Liu, Z.-L.6
Yu, W.7
-
30
-
-
0037121565
-
Photosensitized Diels-Alder reactions of N-arylimines: synthesis of tetrahydroquinoline derivatives
-
Zhang, W.; Jia, X.; Yang, L.; Liu, Z.-L. Photosensitized Diels-Alder reactions of N-arylimines: synthesis of tetrahydroquinoline derivatives. Tetrahedron Lett., 2002, 43, 9433-9436.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 9433-9436
-
-
Zhang, W.1
Jia, X.2
Yang, L.3
Liu, Z.-L.4
-
31
-
-
12344270063
-
Photochemically catalyzed Diels-Alder reaction of arylimines with N-vinylpyrrolidinone and N-vinylcarbazole by 2,4,6-triphenylpyrylium salt: synthesis of 4-heterocycle-substituted tetrahydroquinoline derivatives
-
Zhang, W.; Guo, Y.; Liu, Z.; Jin, X.; Yang, L.; Liu, Z.-L. Photochemically catalyzed Diels-Alder reaction of arylimines with N-vinylpyrrolidinone and N-vinylcarbazole by 2,4,6-triphenylpyrylium salt: synthesis of 4-heterocycle-substituted tetrahydroquinoline derivatives. Tetrahedron, 2005, 61, 1325-1333.
-
(2005)
Tetrahedron
, vol.61
, pp. 1325-1333
-
-
Zhang, W.1
Guo, Y.2
Liu, Z.3
Jin, X.4
Yang, L.5
Liu, Z.-L.6
-
32
-
-
27944471884
-
+) initiated and cation radical-mediated imino Diels-Alder reaction
-
+) initiated and cation radical-mediated imino Diels-Alder reaction. Tetrahedron Lett., 2005, 46, 8937-8939.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 8937-8939
-
-
Zhou, Y.1
Jia, X.2
Li, R.3
Liu, Z.4
Liu, Z.5
Wu, L.6
-
33
-
-
12344256758
-
Intramolecular hetero Diels-Alder (Povarov) approach to the synthesis of the alkaloids luotonin A and camptothecin
-
Twin, H.; Batey, R. A. Intramolecular hetero Diels-Alder (Povarov) approach to the synthesis of the alkaloids luotonin A and camptothecin. Org. Lett., 2004, 6, 4913-4916.
-
(2004)
Org. Lett.
, vol.6
, pp. 4913-4916
-
-
Twin, H.1
Batey, R.A.2
-
34
-
-
67649592788
-
Iron(III)-catalyzed and air-mediated tandem reaction of aldehydes, alkynes and amines: an efficient approach to substituted quinolines
-
Cao, K.; Zhang, F.-M.; Tu, Y.-Q.; Zhuo, X.-T.; Fan, C.-A. Iron(III)-catalyzed and air-mediated tandem reaction of aldehydes, alkynes and amines: an efficient approach to substituted quinolines. Chem. Eur. J., 2009, 15, 6332-6334.
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 6332-6334
-
-
Cao, K.1
Zhang, F.-M.2
Tu, Y.-Q.3
Zhuo, X.-T.4
Fan, C.-A.5
-
35
-
-
0141554100
-
Synthesis of novel steroid alkaloids by cyclization of arylimines from estrone
-
Wölfling, J.; Frank, É.; Schneider, G.; Tietze, L. F. Synthesis of novel steroid alkaloids by cyclization of arylimines from estrone. Eur. J. Org. Chem., 1999, 3013-3020.
-
(1999)
Eur. J. Org. Chem.
, pp. 3013-3020
-
-
Wölfling, J.1
Frank, É.2
Schneider, G.3
Tietze, L.F.4
-
36
-
-
4544374329
-
Synthesis of novel D-secoestrone isoquinuclidines by an unpredicted iminium Ion-induced 1,5-hydride shift
-
Wölfling, J.; Frank, É.; Schneider, G.; Tietze, L. F. Synthesis of novel D-secoestrone isoquinuclidines by an unpredicted iminium Ion-induced 1,5-hydride shift. Eur. J. Org. Chem., 2004, 90-100.
-
(2004)
Eur. J. Org. Chem.
, pp. 90-100
-
-
Wölfling, J.1
Frank, É.2
Schneider, G.3
Tietze, L.F.4
-
37
-
-
67650682825
-
Intramolecular hydro-N-alkylation of hydrazones and oxime ethers: synthesis of novel D-secoestrone isoquinuclidines via domino 1,5-Hydride shift/cyclization
-
Frank, É.; Schneider, G.; Kádár, Z.; Wölfling, J. Intramolecular hydro-N-alkylation of hydrazones and oxime ethers: synthesis of novel D-secoestrone isoquinuclidines via domino 1,5-Hydride shift/cyclization. Eur. J. Org. Chem., 2009, 3544-3553.
-
(2009)
Eur. J. Org. Chem.
, pp. 3544-3553
-
-
Frank, É.1
Schneider, G.2
Kádár, Z.3
Wölfling, J.4
-
38
-
-
67449099159
-
Trifluoroacetic acid-mediated facile construction of 6-substituted phenanthridines
-
Youn, S. W.; Bihn, J. H. Trifluoroacetic acid-mediated facile construction of 6-substituted phenanthridines. Tetrahedron Lett., 2009, 50, 4598-4601.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 4598-4601
-
-
Youn, S.W.1
Bihn, J.H.2
-
39
-
-
0000522529
-
Termination of biomimetic cyclizations by the allylsilane function. Formation of the steroid nucleus in one step from an acyclic polyenic chain
-
Johnson, W. S.; Chen, Y. Q.; Kellogg, M. S. Termination of biomimetic cyclizations by the allylsilane function. Formation of the steroid nucleus in one step from an acyclic polyenic chain. J. Am. Chem. Soc., 1983, 105, 6653-6656.
-
(1983)
J. Am. Chem. Soc.
, vol.105
, pp. 6653-6656
-
-
Johnson, W.S.1
Chen, Y.Q.2
Kellogg, M.S.3
-
40
-
-
41349100916
-
Reactions of N-Acyl imines with dihydropyrans
-
Cakir, S. P.; Mead, K. T. Reactions of N-Acyl imines with dihydropyrans. Synthesis, 2008, 871-874.
-
(2008)
Synthesis
, pp. 871-874
-
-
Cakir, S.P.1
Mead, K.T.2
-
41
-
-
27144508168
-
Straightforward access to a structurally diverse set of oxacyclic scaffolds through a four-component reaction
-
Jiménez, O.; de la Rosa, G.; Lavilla, R. Straightforward access to a structurally diverse set of oxacyclic scaffolds through a four-component reaction. Angew. Chem. Int. Ed., 2005, 44, 6521-6525.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 6521-6525
-
-
Jiménez, O.1
de la Rosa, G.2
Lavilla, R.3
-
42
-
-
0742272064
-
A convenient route to 1-(2-oxiranyl)-1,4-diketones and their application to the synthesis of endobrevicomin, endo-isobrevicomin, frontalin and related compounds via alkylated 6,8-dioxabicyclo[3. 2. 1]octan-2-ones
-
and references cited therein
-
Tyvorskii, V. I.; Astashko, D. A.; Kulinkovich, O. G. A convenient route to 1-(2-oxiranyl)-1,4-diketones and their application to the synthesis of endobrevicomin, endo-isobrevicomin, frontalin and related compounds via alkylated 6,8-dioxabicyclo[3.2.1]octan-2-ones. Tetrahedron, 2004, 60, 1473-1479 and references cited therein.
-
(2004)
Tetrahedron
, vol.60
, pp. 1473-1479
-
-
Tyvorskii, V.I.1
Astashko, D.A.2
Kulinkovich, O.G.3
-
43
-
-
70349914297
-
Building addressable libraries: siteselective lewis acid [Scandium(III)] catalyzed reactions
-
Bi, B.; Maurer, K.; Moeller, K. D. Building addressable libraries: siteselective lewis acid [Scandium(III)] catalyzed reactions. Angew. Chem. Int. Ed., 2009, 48, 5872-5874.
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 5872-5874
-
-
Bi, B.1
Maurer, K.2
Moeller, K.D.3
-
44
-
-
12344317282
-
4-Promoted multicomponent reaction: a new entry to functionalized α-amino acids
-
4-Promoted multicomponent reaction: a new entry to functionalized α-amino acids. Org. Lett., 2005, 7, 7-10.
-
(2005)
Org. Lett.
, vol.7
, pp. 7-10
-
-
Ghosh, A.K.1
Xu, C.-X.2
Kulkarni, S.S.3
Wink, D.4
-
45
-
-
33750060464
-
Asymmetric multicomponent reactions: diastereoselective synthesis of substituted pyrrolidines and prolines
-
Ghosh, A. K.; Kulkarni, S.; Xu, C.-X.; Fanwick, P. E. Asymmetric multicomponent reactions: diastereoselective synthesis of substituted pyrrolidines and prolines. Org. Lett., 2006, 8, 4509-4511.
-
(2006)
Org. Lett.
, vol.8
, pp. 4509-4511
-
-
Ghosh, A.K.1
Kulkarni, S.2
Xu, C.-X.3
Fanwick, P.E.4
-
46
-
-
60749097519
-
A Palladium(II)-catalyzed synthesis of spiroacetals through a one-pot multicomponent cascade reaction
-
Barluenga, J.; Mendoza, A.; Rodríguez, F.; Fañanás, F. J. A Palladium(II)-catalyzed synthesis of spiroacetals through a one-pot multicomponent cascade reaction. Angew. Chem. Int. Ed., 2009, 48, 1644-1647.
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 1644-1647
-
-
Barluenga, J.1
Mendoza, A.2
Rodríguez, F.3
Fañanás, F.J.4
-
47
-
-
60749112064
-
Synthesis of spiroquinolines through a one-pot multicatalytic and multicomponent cascade reaction
-
Barluenga, J.; Mendoza, A.; Rodríguez, F.; Fañanás, F. J. Synthesis of spiroquinolines through a one-pot multicatalytic and multicomponent cascade reaction. Angew. Chem. Int. Ed., 2008, 120, 7152-7155.
-
(2008)
Angew. Chem. Int. Ed.
, vol.120
, pp. 7152-7155
-
-
Barluenga, J.1
Mendoza, A.2
Rodríguez, F.3
Fañanás, F.J.4
-
48
-
-
0037204923
-
3-catalyzed domino reaction of aromatic amines with cyclic enol ethers in water: a highly efficient synthesis of new 1,2,3,4-tetrahydroquinoline derivatives
-
3-catalyzed domino reaction of aromatic amines with cyclic enol ethers in water: a highly efficient synthesis of new 1,2,3,4-tetrahydroquinoline derivatives. J. Org. Chem., 2002, 67, 3969-3971.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 3969-3971
-
-
Zhang, J.1
Li, C.-J.2
-
49
-
-
33646767134
-
A highly efficient synthesis of 1,2,3,4-tetrahydroquinolines by molecular iodine-catalyzed domino reaction of anilines with cyclic enol ethers
-
Lin, X.-F.; Cui, S.-L.; Wang, Y.-G. A highly efficient synthesis of 1,2,3,4-tetrahydroquinolines by molecular iodine-catalyzed domino reaction of anilines with cyclic enol ethers. Tetrahedron Lett., 2006, 47, 4509-4512.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 4509-4512
-
-
Lin, X.-F.1
Cui, S.-L.2
Wang, Y.-G.3
-
50
-
-
0012815011
-
Total synthesis of the alkaloids martinelline and martinellic acid via a hetero diels-alder multicomponent coupling reaction
-
Powell, D. A.; Batey, R. A. Total synthesis of the alkaloids martinelline and martinellic acid via a hetero diels-alder multicomponent coupling reaction. Org. Lett., 2002, 4, 2913-2916.
-
(2002)
Org. Lett.
, vol.4
, pp. 2913-2916
-
-
Powell, D.A.1
Batey, R.A.2
-
51
-
-
33846579646
-
A substrate-based folding process incorporating chemodifferentiating ABB' three-component reactions of terminal alkynoates and 1,2-Dicarbonyl compounds: a skeletal-diversity-oriented synthetic manifold
-
Tejedor, D.; Santos-Expósito, A.; García-Tellado, F. A substrate-based folding process incorporating chemodifferentiating ABB' three-component reactions of terminal alkynoates and 1,2-Dicarbonyl compounds: a skeletal-diversity-oriented synthetic manifold. Chem. Eur. J., 2007, 13, 1201-1209.
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 1201-1209
-
-
Tejedor, D.1
Santos-Expósito, A.2
García-Tellado, F.3
-
52
-
-
0344861842
-
Domino reaction of anilines with 3,4-dihydro-2H-pyran catalyzed by cation-exchange resin in water: an efficient synthesis of 1,2,3,4-tetrahydroquinoline derivatives
-
Chen, L.; Li, C.-J. Domino reaction of anilines with 3,4-dihydro-2H-pyran catalyzed by cation-exchange resin in water: an efficient synthesis of 1,2,3,4-tetrahydroquinoline derivatives. Green Chem., 2003, 5, 627-629.
-
(2003)
Green Chem.
, vol.5
, pp. 627-629
-
-
Chen, L.1
Li, C.-J.2
-
53
-
-
0037140820
-
Montmorillonite clay-catalyzed [4+2] cycloaddition reactions: a facile synthesis of pyrano-and furanoquinolines
-
Yadav, J. S.; Reddy, B. V. S.; Sadasiv, K.; Reddy, P. S. R. Montmorillonite clay-catalyzed [4+2] cycloaddition reactions: a facile synthesis of pyrano-and furanoquinolines. Tetrahedron Lett., 2002, 43, 3853-3856.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 3853-3856
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Sadasiv, K.3
Reddy, P.S.R.4
-
54
-
-
33845335853
-
CAN-catalyzed three-component reaction between anilines and alkyl vinyl ethers: stereoselective synthesis of 2-methyl-1,2,3,4-tetrahydroquinolines and studies on their aromatization
-
Sridharan, V.; Avendaño, C.; Menéndez, J. C. CAN-catalyzed three-component reaction between anilines and alkyl vinyl ethers: stereoselective synthesis of 2-methyl-1,2,3,4-tetrahydroquinolines and studies on their aromatization. Tetrahedron, 2007, 63, 673-681.
-
(2007)
Tetrahedron
, vol.63
, pp. 673-681
-
-
Sridharan, V.1
Avendaño, C.2
Menéndez, J.C.3
-
55
-
-
0033531748
-
A three-component coupling protocol for the synthesis of substituted hexahydropyr-rolo[3,2-c]quinolines
-
Batey, R. A.; Simoncic, P. D.; Lin, D.; Smyj, R. P.; Lough, A. J. A three-component coupling protocol for the synthesis of substituted hexahydropyr-rolo[3,2-c]quinolines. Chem. Commun., 1999, 651-652.
-
(1999)
Chem. Commun.
, pp. 651-652
-
-
Batey, R.A.1
Simoncic, P.D.2
Lin, D.3
Smyj, R.P.4
Lough, A.J.5
-
56
-
-
0037213014
-
3-catalyzed reaction of aromatic amines with cyclic hemiacetals in water: facile synthesis 1,2,3,4-tetrahydroquinoline derivatives
-
3-catalyzed reaction of aromatic amines with cyclic hemiacetals in water: facile synthesis 1,2,3,4-tetrahydroquinoline derivatives. Tetrahedron Lett., 2003, 44, 153-156.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 153-156
-
-
Li, Z.1
Zhang, J.2
Li, C.-J.3
-
57
-
-
0034685750
-
A stereoselective route to polysubstituted tetrahydroquinolines by benzotriazole-promoted condensation of aliphatic aldehydes and aromatic amines
-
Talukdar, S.; Chen, C.-T.; Fang, J.-M. A stereoselective route to polysubstituted tetrahydroquinolines by benzotriazole-promoted condensation of aliphatic aldehydes and aromatic amines. J. Org. Chem., 2000, 65, 3148-3153.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 3148-3153
-
-
Talukdar, S.1
Chen, C.-T.2
Fang, J.-M.3
-
58
-
-
0141518222
-
Lanthanide(III)-catalyzed multi-component aza-Diels-Alder reaction of aliphatic N-arylaldimines with cyclopentadiene
-
Powell, D. A.; Batey, R. A. Lanthanide(III)-catalyzed multi-component aza-Diels-Alder reaction of aliphatic N-arylaldimines with cyclopentadiene. Tetrahedron Lett., 2003, 44, 7569-7573.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 7569-7573
-
-
Powell, D.A.1
Batey, R.A.2
-
59
-
-
33947512724
-
An efficient synthesis of isoindolo[2,1-a]quinoline derivatives via imino diels-alder and intramolecular diels-alder reactions with furan
-
Kouznetsov, V. V.; Cruz, U. M.; Zubkov, F. I.; Nikitina, E. V. An efficient synthesis of isoindolo[2,1-a]quinoline derivatives via imino diels-alder and intramolecular diels-alder reactions with furan. Synthesis, 2007, 375-384.
-
(2007)
Synthesis
, pp. 375-384
-
-
Kouznetsov, V.V.1
Cruz, U.M.2
Zubkov, F.I.3
Nikitina, E.V.4
-
60
-
-
22644432437
-
A facile synthesis of isoindolo[2,1-a]quinolin-11-one via [4+2] reactions of N-acyliminium intermediates with olefines
-
Zhang, W.; Zheng, A.; Liu, Z.; Yang, L.; Liu, Z. A facile synthesis of isoindolo[2,1-a]quinolin-11-one via [4+2] reactions of N-acyliminium intermediates with olefines. Tetrahedron Lett., 2005, 46, 5691-5694.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 5691-5694
-
-
Zhang, W.1
Zheng, A.2
Liu, Z.3
Yang, L.4
Liu, Z.5
-
61
-
-
58849165439
-
A one-pot synthetic approach to the functionalized isomeric ellipticine derivatives through an imino Diels-Alder reaction
-
Gaddam, V.; Nagarajan, R. A one-pot synthetic approach to the functionalized isomeric ellipticine derivatives through an imino Diels-Alder reaction. Tetrahedron Lett., 2009, 50, 1243-1248.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 1243-1248
-
-
Gaddam, V.1
Nagarajan, R.2
-
62
-
-
55249117944
-
Povarov reactions involving 3-Aminocoumarins: synthesis of 1,2,3,4-Tetrahydropyrido[2,3-c]coumarins and Pyrido[2,3-c]coumarins
-
Kudale, A. A.; Kendall, J.; Miller, D. O.; Collins, J. L.; Bodwell, G. J. Povarov reactions involving 3-Aminocoumarins: synthesis of 1,2,3,4-Tetrahydropyrido[2,3-c]coumarins and Pyrido[2,3-c]coumarins. J. Org. Chem., 2008, 73, 8437-8447.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 8437-8447
-
-
Kudale, A.A.1
Kendall, J.2
Miller, D.O.3
Collins, J.L.4
Bodwell, G.J.5
-
63
-
-
0041345738
-
Useful dual diels-alder behavior of 2-Azetidinone-Tethered aryl imines as azadienophiles or azadienes: a β-Lactam-Based stereocontrolled access to optically pure highly functionalized indolizidine systems
-
Alcaide, B.; Almendros, P.; Alonso, J. M.; Aly, M. F. Useful dual diels-alder behavior of 2-Azetidinone-Tethered aryl imines as azadienophiles or azadienes: a β-Lactam-Based stereocontrolled access to optically pure highly functionalized indolizidine systems. Chem. Eur. J., 2003, 9, 3415-3426.
-
(2003)
Chem. Eur. J.
, vol.9
, pp. 3415-3426
-
-
Alcaide, B.1
Almendros, P.2
Alonso, J.M.3
Aly, M.F.4
-
64
-
-
33846335486
-
Multicomponent coupling reactions of N-acetyl-2-azetine
-
Stevenson, P. J.; Nieuwenhuyzen, M.; Osborne, D. Multicomponent coupling reactions of N-acetyl-2-azetine. Arkivoc, 2007, 129-144.
-
(2007)
Arkivoc
, pp. 129-144
-
-
Stevenson, P.J.1
Nieuwenhuyzen, M.2
Osborne, D.3
-
65
-
-
34247587011
-
The first aza Diels-Alder reaction involving an α.β-unsaturated hydrazone as the dienophile: stereoselective synthesis of C-4 functionalized 1,2,3,4-tetrahydroquinolines containing a quaternary stereocenter
-
Sridharan, V.; Perumal, P. T.; Avendaño, C.; Menéndez, J. C. The first aza Diels-Alder reaction involving an α.β-unsaturated hydrazone as the dienophile: stereoselective synthesis of C-4 functionalized 1,2,3,4-tetrahydroquinolines containing a quaternary stereocenter. Org. Biomol. Chem., 2007, 5, 1351-1353.
-
(2007)
Org. Biomol. Chem.
, vol.5
, pp. 1351-1353
-
-
Sridharan, V.1
Perumal, P.T.2
Avendaño, C.3
Menéndez, J.C.4
-
66
-
-
3242716697
-
Unprecedented regio and stereocontrol in Povarov reaction of benzylidene-(3-nitrophenyl)amine
-
Stevenson, P. J.; Graham, I. Unprecedented regio and stereocontrol in Povarov reaction of benzylidene-(3-nitrophenyl)amine. Arkivoc, 2003, 139-144.
-
(2003)
Arkivoc
, pp. 139-144
-
-
Stevenson, P.J.1
Graham, I.2
-
67
-
-
66249113161
-
Multicomponent reactions of indole, ethyl glyoxylate and anilines: from friedel-crafts to Aza-Diels-Alder reactions catalysed by scandium triflate
-
Desimoni, G.; Faita, G.; Mella, M.; Toscanini, M.; Boiocchi, M. Multicomponent reactions of indole, ethyl glyoxylate and anilines: from friedel-crafts to Aza-Diels-Alder reactions catalysed by scandium triflate. Eur. J. Org. Chem., 2009, 2627-2634.
-
(2009)
Eur. J. Org. Chem.
, pp. 2627-2634
-
-
Desimoni, G.1
Faita, G.2
Mella, M.3
Toscanini, M.4
Boiocchi, M.5
-
68
-
-
35548962875
-
Enol esters: versatile substrates for mannich-type multicomponent reactions
-
Isambert, N.; Cruz, M.; Arévalo, M. J.; Gómez, E.; Lavilla, R. Enol esters: versatile substrates for mannich-type multicomponent reactions. Org. Lett., 2007, 9, 4199-4202.
-
(2007)
Org. Lett.
, vol.9
, pp. 4199-4202
-
-
Isambert, N.1
Cruz, M.2
Arévalo, M.J.3
Gómez, E.4
Lavilla, R.5
-
69
-
-
33751386243
-
Intramolecular hetero-Diels-Alder reaction of N-arylimines. Applications to the synthesis of octahydroacridine derivatives
-
Laschat, S.; Lauterwein, J. Intramolecular hetero-Diels-Alder reaction of N-arylimines. Applications to the synthesis of octahydroacridine derivatives. J. Org. Chem., 2002, 58, 2856-2861.
-
(2002)
J. Org. Chem.
, vol.58
, pp. 2856-2861
-
-
Laschat, S.1
Lauterwein, J.2
-
70
-
-
40849130002
-
Indium chloride catalyzed intramolecular cyclization of N-aryl imines: synthesis of pyrrolo[2,3-d]pyrimidine annulated tetrahydroquinoline derivatives
-
Ramesh, E.; Raghunathan, R. Indium chloride catalyzed intramolecular cyclization of N-aryl imines: synthesis of pyrrolo[2,3-d]pyrimidine annulated tetrahydroquinoline derivatives. Tetrahedron Lett., 2008, 49, 2583-2587.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 2583-2587
-
-
Ramesh, E.1
Raghunathan, R.2
-
71
-
-
47049114333
-
An efficient, one-pot synthesis of isomeric ellipticine derivatives through intramolecular Imino-Diels-Alder reaction
-
Gaddam, V.; Nagarajan, R. An efficient, one-pot synthesis of isomeric ellipticine derivatives through intramolecular Imino-Diels-Alder reaction. Org. Lett., 2008, 10, 1975-1978.
-
(2008)
Org. Lett.
, vol.10
, pp. 1975-1978
-
-
Gaddam, V.1
Nagarajan, R.2
-
72
-
-
0347132250
-
Dihydropyridines in MCRs. tandem processes leading to modular tetrahydroquinoline systems with up to 6 diversity elements
-
Lavilla, R.; Carranco, I.; Díaz, J. L.; Bernabeu, M.; de la Rosa, G. Dihydropyridines in MCRs. tandem processes leading to modular tetrahydroquinoline systems with up to 6 diversity elements. Mol. Divers., 2003, 6, 171-175.
-
(2003)
Mol. Divers.
, vol.6
, pp. 171-175
-
-
Lavilla, R.1
Carranco, I.2
Díaz, J.L.3
Bernabeu, M.4
de la Rosa, G.5
-
73
-
-
33747047578
-
Facile synthesis of tetrahydroquinolines and julolidines through multicomponent reaction
-
Legros, J.; Crousse, B.; Ourévitch, M.; Bonnet-Delpon, D. Facile synthesis of tetrahydroquinolines and julolidines through multicomponent reaction. Synlett, 2006, 1899-1902.
-
(2006)
Synlett
, pp. 1899-1902
-
-
Legros, J.1
Crousse, B.2
Ourévitch, M.3
Bonnet-Delpon, D.4
-
74
-
-
17144366282
-
Asymmetric multicomponent reactions (AMCRs): the new frontier
-
Ramón, D. J.; Yus, M. Asymmetric multicomponent reactions (AMCRs): the new frontier. Angew. Chem. Int. Ed., 2005, 44, 1602-1634.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 1602-1634
-
-
Ramón, D.J.1
Yus, M.2
-
75
-
-
0030573985
-
Catalytic asymmetric aza Diels-Alder reactions using a chiral lanthanide Lewis acid. Enantioselective synthesis of tetrahydroquinoline derivatives using a catalytic amount of a chiral source
-
Ishitani, H.; Kobayashi, S. Catalytic asymmetric aza Diels-Alder reactions using a chiral lanthanide Lewis acid. Enantioselective synthesis of tetrahydroquinoline derivatives using a catalytic amount of a chiral source. Tetrahedron Lett., 1996, 37, 7357-7360.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 7357-7360
-
-
Ishitani, H.1
Kobayashi, S.2
-
76
-
-
33749522044
-
Chiral bronsted acid-catalyzed inverse electron-demand Aza Diels-Alder reaction
-
Akiyama, T.; Morita, H.; Fuchibe, K. Chiral bronsted acid-catalyzed inverse electron-demand Aza Diels-Alder reaction. J. Am. Chem. Soc., 2006, 128, 13070-13071.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 13070-13071
-
-
Akiyama, T.1
Morita, H.2
Fuchibe, K.3
-
77
-
-
66349134696
-
Highly enantioselective one-pot, three-component mannich-type reaction catalyzed by an N-N'-Dioxide-Scandium(III) complex
-
Chen, S.; Hou, Z.; Zhu, Y.; Wang, J.; Lili, L.; Liu, X.; Feng, X. Highly enantioselective one-pot, three-component mannich-type reaction catalyzed by an N-N'-Dioxide-Scandium(III) complex. Chem. Eur. J., 2009, 15, 5884-5887.
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 5884-5887
-
-
Chen, S.1
Hou, Z.2
Zhu, Y.3
Wang, J.4
Lili, L.5
Liu, X.6
Feng, X.7
-
78
-
-
67749110116
-
Chiral bronsted acid-catalyzed enantioselective three-component povarov reaction
-
Liu, H.; Dagousset, G.; Masson, G.; Retailleau, P.; Zhu, J. Chiral bronsted acid-catalyzed enantioselective three-component povarov reaction. J. Am. Chem. Soc., 2009, 131, 4598-4599.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 4598-4599
-
-
Liu, H.1
Dagousset, G.2
Masson, G.3
Retailleau, P.4
Zhu, J.5
-
79
-
-
0035963686
-
First asymmetric synthesis of quinoline derivatives by inverse electron demand (IED) diels-alder reaction using chiral Ti(IV) complex
-
Sundararajan, G.; Prabagaran, N.; Varghese, B. First asymmetric synthesis of quinoline derivatives by inverse electron demand (IED) diels-alder reaction using chiral Ti(IV) complex. Org. Lett., 2001, 3, 1973-1976.
-
(2001)
Org. Lett.
, vol.3
, pp. 1973-1976
-
-
Sundararajan, G.1
Prabagaran, N.2
Varghese, B.3
-
80
-
-
0037147795
-
Potent in vitro methicillin-resistant Staphylococcus aureus activity of 2-(1H-indol-3-yl)tetrahydroquinoline derivatives
-
Hoemann, M. Z.; Xie, R. L.; Rossi, R. F.; Meyer, S.; Sidhu, A.; Cuny, G. D.; Hauske, J. R. Potent in vitro methicillin-resistant Staphylococcus aureus activity of 2-(1H-indol-3-yl)tetrahydroquinoline derivatives. Bioorg. Med. Chem. Lett., 2002, 12, 129-132.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 129-132
-
-
Hoemann, M.Z.1
Xie, R.L.2
Rossi, R.F.3
Meyer, S.4
Sidhu, A.5
Cuny, G.D.6
Hauske, J.R.7
-
81
-
-
33750123139
-
Acid-mediated three-component aza-Diels-Alder reactions of 2-aminophenols under controlled microwave heating for synthesis of highly functionalized tetrahydroquinolines. Part 9: Chemistry of aminophenols
-
Xing, X.; Wu, J.; Dai, W.-M. Acid-mediated three-component aza-Diels-Alder reactions of 2-aminophenols under controlled microwave heating for synthesis of highly functionalized tetrahydroquinolines. Part 9: Chemistry of aminophenols. Tetrahedron, 2006, 62, 11200-11206.
-
(2006)
Tetrahedron
, vol.62
, pp. 11200-11206
-
-
Xing, X.1
Wu, J.2
Dai, W.-M.3
-
82
-
-
36649019120
-
Ionic liquid phase synthesis of tetrahydropyrano-and tetrahydrofuranoquinolines under microwave irradiation
-
Li, M.; Sun, E.; Wen, L.; Sun, J.; Li, Y.; Yang, H. Ionic liquid phase synthesis of tetrahydropyrano-and tetrahydrofuranoquinolines under microwave irradiation. J. Comb. Chem., 2007, 9, 903-905.
-
(2007)
J. Comb. Chem.
, vol.9
, pp. 903-905
-
-
Li, M.1
Sun, E.2
Wen, L.3
Sun, J.4
Li, Y.5
Yang, H.6
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