-
1
-
-
67650237241
-
-
Mohamed, E. A. Some new quinolones of expected pharmaceutical importance derived from 1,2-dihydro-4-hydro-1-methyl-2-oxoquinoline-3- carboxaldehyde. Chem. Pap. 1994, 48, 261-267; Chem. Abstr. 1995, 9315x.
-
Mohamed, E. A. Some new quinolones of expected pharmaceutical importance derived from 1,2-dihydro-4-hydro-1-methyl-2-oxoquinoline-3- carboxaldehyde. Chem. Pap. 1994, 48, 261-267; Chem. Abstr. 1995, 9315x.
-
-
-
-
2
-
-
67650246222
-
-
Nesterova, I. N.; Alekseeva, L. M.; Andreeva, L. M.; Andreeva, N. I.; Golovina, S. M.; Granik, V. G. Synthesis and pharmacological activity of derivatives of 5-(dimethylamino)pyrano (3,2-c)quinoline-2 ones. Khim.-Farm Zh. 1995, 29, 31-34; Chem. Abst. 1996, 124, 117128t.
-
Nesterova, I. N.; Alekseeva, L. M.; Andreeva, L. M.; Andreeva, N. I.; Golovina, S. M.; Granik, V. G. Synthesis and pharmacological activity of derivatives of 5-(dimethylamino)pyrano (3,2-c)quinoline-2 ones. Khim.-Farm Zh. 1995, 29, 31-34; Chem. Abst. 1996, 124, 117128t.
-
-
-
-
3
-
-
0021733921
-
Nonsteroidal anti-inflammatory agents: Synthesis of 4-hydrox-2-oxo-1,2-dihydroquinoline-3-ylalkanoic acids by the Witting reaction of quinisatins
-
Faber, K.; Stueckler, H.; Kappe, T. Nonsteroidal anti-inflammatory agents: Synthesis of 4-hydrox-2-oxo-1,2-dihydroquinoline-3-ylalkanoic acids by the Witting reaction of quinisatins. J. Heterocycl. Chem. 1984, 21, 1177-1181.
-
(1984)
J. Heterocycl. Chem
, vol.21
, pp. 1177-1181
-
-
Faber, K.1
Stueckler, H.2
Kappe, T.3
-
4
-
-
0025327614
-
Differential analysis of the frequency dependent effects of class I antiarrthymic drugs according to periodical ligand binding: Implication for antiarrthymic and proarrthymics
-
Weirich, J.; Antoni, H. Differential analysis of the frequency dependent effects of class I antiarrthymic drugs according to periodical ligand binding: Implication for antiarrthymic and proarrthymics. J. Cardiovasc. Pharmacol. 1990, 15, 998-1009.
-
(1990)
J. Cardiovasc. Pharmacol
, vol.15
, pp. 998-1009
-
-
Weirich, J.1
Antoni, H.2
-
5
-
-
67650240256
-
-
Khodzhaeva, K. S. A.; Bessonova, I. A. Some data on the relation between chemical structure and estrogen activity in a series of quinoline derivatives. Dokl. Akad. Nauk Uzh, SSR 1982, 9, 34-36; Chem. Abstr. 1983, 98, 83727q.
-
Khodzhaeva, K. S. A.; Bessonova, I. A. Some data on the relation between chemical structure and estrogen activity in a series of quinoline derivatives. Dokl. Akad. Nauk Uzh, SSR 1982, 9, 34-36; Chem. Abstr. 1983, 98, 83727q.
-
-
-
-
6
-
-
31144434114
-
Preparation of tetra- hydroquinolines as immunosuppressants and inflammation inhibitors. Kokai Tokkayo Koho JP 06 56,788
-
Kono, Y.; Kojima, E.; Saito, K.; Kudo, S.; Sekoe, Y. Preparation of tetra- hydroquinolines as immunosuppressants and inflammation inhibitors. Kokai Tokkayo Koho JP 06 56,788; Chem. Abstr. 1994, 121, 157536u.
-
(1994)
Chem. Abstr
, vol.121
-
-
Kono, Y.1
Kojima, E.2
Saito, K.3
Kudo, S.4
Sekoe, Y.5
-
7
-
-
0026749637
-
2-Carboxytetrahydroquinolines: Conformational and sterochemical requirements for antagonism of the gly- cine site on the NMDA receptor
-
(a) Carling, R. W.; Leeson, P. D.; Moseley, A. M.; Baker, R.; Forster, A. C.; Grimwood, S.; Kemp, J. A.; Marshall, G. R. 2-Carboxytetrahydroquinolines: Conformational and sterochemical requirements for antagonism of the gly- cine site on the NMDA receptor. J. Med. Chem. 1992, 35, 1942
-
(1992)
J. Med. Chem
, vol.35
, pp. 1942
-
-
Carling, R.W.1
Leeson, P.D.2
Moseley, A.M.3
Baker, R.4
Forster, A.C.5
Grimwood, S.6
Kemp, J.A.7
Marshall, G.R.8
-
8
-
-
0026766273
-
4-Amido-2-carboxytetrahydroquino- lines: Structure-activity relationships for antagonism at the glycine site of the NMDA receptor
-
(b) Leeson, P. D.; Carling, R. W.; Moore, K. W.; Moseley, A. M.; Smith, J. D.; Stevenson, G.; Chan, T.; Baker, R.; Foster, A. C.; Grimword, S.; Kemp, J. A.; Marshall, G. R.; Hoogsteen, K. 4-Amido-2-carboxytetrahydroquino- lines: Structure-activity relationships for antagonism at the glycine site of the NMDA receptor. J. Med. Chem. 1992, 35, 1954
-
(1992)
J. Med. Chem
, vol.35
, pp. 1954
-
-
Leeson, P.D.1
Carling, R.W.2
Moore, K.W.3
Moseley, A.M.4
Smith, J.D.5
Stevenson, G.6
Chan, T.7
Baker, R.8
Foster, A.C.9
Grimword, S.10
Kemp, J.A.11
Marshall, G.R.12
Hoogsteen, K.13
-
9
-
-
67650230758
-
-
Cai, S. X, Zhou, Z.-L, Huang, J.-C, Whittermore, E. R, Egbuwoku, Z. O, Lu, Y, Hawkinson, J. E, Woodward, R. M, Keana, J. F. W. Synthesis and structure-activity
-
(c) Cai, S. X.; Zhou, Z.-L.; Huang, J.-C.; Whittermore, E. R.; Egbuwoku, Z. O.; Lu, Y.; Hawkinson, J. E.; Woodward, R. M.; Keana, J. F. W. Synthesis and structure-activity
-
-
-
-
10
-
-
0000039703
-
-
relationships of 1,2,3,4-tetrahydroquinoline-2,3,4-trione-3-oxime novel and highly potent antagonists for NMDA receptor glucine site. J. Med. Chem. 1996, 39, 3248.
-
relationships of 1,2,3,4-tetrahydroquinoline-2,3,4-trione-3-oxime novel and highly potent antagonists for NMDA receptor glucine site. J. Med. Chem. 1996, 39, 3248.
-
-
-
-
11
-
-
0036157389
-
Antiplasmodial and cytotoxic activity of galipinine and other tetrahydroquinolines from Galipea officinalis
-
Jacquemond-Collet, I.; Benoit-Vical, F.; Mustofa, V.; Stanislas, A.; Mallie, E.; Fouraste, I. Antiplasmodial and cytotoxic activity of galipinine and other tetrahydroquinolines from Galipea officinalis. Planta Med. 2002, 68, 68.
-
(2002)
Planta Med
, vol.68
, pp. 68
-
-
Jacquemond-Collet, I.1
Benoit-Vical, F.2
Mustofa, V.3
Stanislas, A.4
Mallie, E.5
Fouraste, I.6
-
12
-
-
0034193404
-
New quinolinic derivatives as centrally active antioxidants: First QSAR report on FSH receptor antagonistic activity: Quantitative investigations on physico-chemical and structural features among 6-amino-4-phenyltetrahydroquinoline derivatives
-
Dorey, G.; Lockhart, B.; Lestage, P.; Casara, P. New quinolinic derivatives as centrally active antioxidants: First QSAR report on FSH receptor antagonistic activity: Quantitative investigations on physico-chemical and structural features among 6-amino-4-phenyltetrahydroquinoline derivatives. Bioorg. Med. Chem. 2000, 10, 935-939.
-
(2000)
Bioorg. Med. Chem
, vol.10
, pp. 935-939
-
-
Dorey, G.1
Lockhart, B.2
Lestage, P.3
Casara, P.4
-
13
-
-
24344504883
-
First QSAR report on FSH receptor antagonistic activity: Quantitative investigations on physico-chemical and structural features among 6-amino-4-phenyltetrahydroquinoline derivatives
-
(a) Manivannan, E.; Prasanna, S. First QSAR report on FSH receptor antagonistic activity: Quantitative investigations on physico-chemical and structural features among 6-amino-4-phenyltetrahydroquinoline derivatives. Bioorg. Med. Chem. Lett. 2005, 15, 4496-4501
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 4496-4501
-
-
Manivannan, E.1
Prasanna, S.2
-
14
-
-
20144367831
-
Identification of substituted 6-amino-4- phenyltetrahydroquinoline derivatives: Potent antagonists for the follicle-stimulating hormone receptor
-
(b) van Straten, N. C. R.; van Berkel, T. H. J.; Demont, D. R.; Karstens, W.-J. F.; Merkx, R.; Oos- terom, J.; van Someren, R. G.; Timmers, C. M.; van zandvoort, P. M. Identification of substituted 6-amino-4- phenyltetrahydroquinoline derivatives: Potent antagonists for the follicle-stimulating hormone receptor. J. Med. Chem. 2005, 48, 1697-1700.
-
(2005)
J. Med. Chem
, vol.48
, pp. 1697-1700
-
-
van Straten, N.C.R.1
van Berkel, T.H.J.2
Demont, D.R.3
Karstens, W.-J.F.4
Merkx, R.5
Oos- terom, J.6
van Someren, R.G.7
Timmers, C.M.8
van zandvoort, P.M.9
-
15
-
-
1842741033
-
Highly diasteroselctive inverse electron demand (IED) Diels-Alder reaction mediated by chiral salen-AlCl complex: The first target-oriented synthesis of pyranoquinolines as potential antibacterial agents
-
Magesh, C. J.; Makesh, S. V.; Perumal, P. T. Highly diasteroselctive inverse electron demand (IED) Diels-Alder reaction mediated by chiral salen-AlCl complex: The first target-oriented synthesis of pyranoquinolines as potential antibacterial agents. Bioorg. Med. Chem. Lett. 2004, 14, 2035-2040.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 2035-2040
-
-
Magesh, C.J.1
Makesh, S.V.2
Perumal, P.T.3
-
16
-
-
0030602266
-
-
Kartrizky, A. R.; Rachwal, S.; Rachwal, B. Recent progress in the synth esis of 1,2,3,4-tetrahydroquinolines. Tetrahedron 1996, 52, 15031-15070
-
(a) Kartrizky, A. R.; Rachwal, S.; Rachwal, B. Recent progress in the synth esis of 1,2,3,4-tetrahydroquinolines. Tetrahedron 1996, 52, 15031-15070
-
-
-
-
17
-
-
0042912898
-
Cation radical imino Diels-Alder reaction: A new approach for the synthesis of tet- rahydroquinolines
-
(b) Jia, X. D.; Lin, H. C.; Huo, C. D.; Zhang, W.; Lu, J. M.; Lin, H. C.; Huo, C. D.; Zhang, W.; Lu, J. M.; Yang, L.; Zhao, G. Y.; Liu, Z. L. Cation radical imino Diels-Alder reaction: A new approach for the synthesis of tet- rahydroquinolines. Synlett 2003, 1707
-
(2003)
Synlett
, pp. 1707
-
-
Jia, X.D.1
Lin, H.C.2
Huo, C.D.3
Zhang, W.4
Lu, J.M.5
Lin, H.C.6
Huo, C.D.7
Zhang, W.8
Lu, J.M.9
Yang, L.10
Zhao, G.Y.11
Liu, Z.L.12
-
18
-
-
0033953146
-
Imino Diels-Alder reaction: Application to the synthesis of diverse cyclopenta[c]quinoline derivatives
-
(c) Posson, H.; Hurvois, J. P.; Moinet, C. Imino Diels-Alder reaction: Application to the synthesis of diverse cyclopenta[c]quinoline derivatives. Synlett 2000, 209
-
(2000)
Synlett
, pp. 209
-
-
Posson, H.1
Hurvois, J.P.2
Moinet, C.3
-
19
-
-
0037121565
-
Photosensitized Diels-Alder reactions of N-aryli- mines: Synthesis of tetrahydroquinoline derivatives
-
(d) Zhang, W.; Jia, X.; Yang, L.; Liu, Z. L. Photosensitized Diels-Alder reactions of N-aryli- mines: Synthesis of tetrahydroquinoline derivatives. Tetrahedron Lett. 2002,43, 9433.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 9433
-
-
Zhang, W.1
Jia, X.2
Yang, L.3
Liu, Z.L.4
-
20
-
-
0032516298
-
Convenient synthesis of pyrano [3,2-c]quinolines and indeno [2,1-c] quinolines by imino Diels-Alder reactions
-
Babu, G.; Perumal, P. T. Convenient synthesis of pyrano [3,2-c]quinolines and indeno [2,1-c] quinolines by imino Diels-Alder reactions. Tetrahedron Lett. 1998, 39, 3225-3228.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 3225-3228
-
-
Babu, G.1
Perumal, P.T.2
-
21
-
-
0029123197
-
Yetter- biumtriflate-catalyzed synthesis of quinoline derivatives from N-arylaldi- mines and vinyl ethers
-
(a) Makoika, Y.; Shindo, T.; Tanigudi, Y.; Takki, K.; Fujwara, Y. Yetter- biumtriflate-catalyzed synthesis of quinoline derivatives from N-arylaldi- mines and vinyl ethers. Synthesis 1995, 801
-
(1995)
Synthesis
, pp. 801
-
-
Makoika, Y.1
Shindo, T.2
Tanigudi, Y.3
Takki, K.4
Fujwara, Y.5
-
22
-
-
0030829336
-
-
Annuziata, R.; Ciquini, M.; Cozzi, F.; Molteni, V.; Schupp, O. A new multicomponent synthesis of 1,2,3,4-tetrahydroqunilines. Tetrahedron 1997, 53, 9715
-
(b) Annuziata, R.; Ciquini, M.; Cozzi, F.; Molteni, V.; Schupp, O. A new multicomponent synthesis of 1,2,3,4-tetrahydroqunilines. Tetrahedron 1997, 53, 9715
-
-
-
-
24
-
-
67650222025
-
-
Ishitani, H, Kobayashi, S. Catalytic asymmetric aza-Diels-Alder
-
(d) Ishitani, H.; Kobayashi, S. Catalytic asymmetric aza-Diels-Alder
-
-
-
-
25
-
-
0030573985
-
reactions using a chiral lanthanide Lewis acid. Enantioselective synthesis of tetrahydroquinoline derivatives using a catalytic amount of a chiral source
-
reactions using a chiral lanthanide Lewis acid. Enantioselective synthesis of tetrahydroquinoline derivatives using a catalytic amount of a chiral source. Tetrahedron Lett. 1996, 118, 7357.
-
(1996)
Tetrahedron Lett
, vol.118
, pp. 7357
-
-
-
26
-
-
0041753278
-
Activation of imines by rare earth metal triflates. Ln(OTf)3 or Sc(OTf)3-catalyzed reactions of imines with silyl enolates and Diels-Alder reactions of imines
-
(a) Kobayashi, S.; Araki, M.; Ishitani, H.; Nagayama, S.; Hachiya, I. Activation of imines by rare earth metal triflates. Ln(OTf)3 or Sc(OTf)3-catalyzed reactions of imines with silyl enolates and Diels-Alder reactions of imines. Synlett 1995, 223
-
(1995)
Synlett
, pp. 223
-
-
Kobayashi, S.1
Araki, M.2
Ishitani, H.3
Nagayama, S.4
Hachiya, I.5
-
27
-
-
0029813591
-
A new methodology for combinatorial synthesis: Preparation of diverse quinoline derivatives using a novel polymer-supported scandium catalyst
-
(b) Kobayashi, S.; Nagayama, S. A new methodology for combinatorial synthesis: Preparation of diverse quinoline derivatives using a novel polymer-supported scandium catalyst. J. Am. Chem. Soc. 1996, 118, 8977
-
(1996)
J. Am. Chem. Soc
, vol.118
, pp. 8977
-
-
Kobayashi, S.1
Nagayama, S.2
-
28
-
-
0036459071
-
Scandium triflate immobilized in ionic liquids: A novel and recyclable catalytic system for Hetero-Diels-Alder reactions
-
(c) Yadav, J. S.; Reddy, B. V. S.; Gayathri, K. U.; Prasad, A. R. Scandium triflate immobilized in ionic liquids: A novel and recyclable catalytic system for Hetero-Diels-Alder reactions. Synthesis 2002, 2537.
-
(2002)
Synthesis
, pp. 2537
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Gayathri, K.U.3
Prasad, A.R.4
-
29
-
-
67650237239
-
-
Povarov, L. S. aα/&ß;-Unsaturated ethers and their analogues in reactions of diene synthesis. Russ. Chem. Rev. 1967, 36, 656.
-
Povarov, L. S. aα/&ß;-Unsaturated ethers and their analogues in reactions of diene synthesis. Russ. Chem. Rev. 1967, 36, 656.
-
-
-
-
30
-
-
0033588330
-
Lanthanide chloride catalyzed Diels- Alder reaction: One-pot synthesis of pyrano [3,2-c]- and furo [3,2-c] quino- lines
-
Ma, Y.; Qian, C. T.; Xie, M. H.; Sun, J. Lanthanide chloride catalyzed Diels- Alder reaction: One-pot synthesis of pyrano [3,2-c]- and furo [3,2-c] quino- lines. J. Org. Chem. 1999, 64, 6462.
-
(1999)
J. Org. Chem
, vol.64
, pp. 6462
-
-
Ma, Y.1
Qian, C.T.2
Xie, M.H.3
Sun, J.4
-
31
-
-
0035128465
-
Lithium perchlorate/diethylether catalyzed aza-Diels-Alder reaction: An expeditious synthesis of pyrano, indeno quinolines, and phenanthridines
-
Yadav, J. S.; Subba Reddy, B. V.; Srinivas, R.; Madhuri, C. H.; Ramalingam, T. Lithium perchlorate/diethylether catalyzed aza-Diels-Alder reaction: An expeditious synthesis of pyrano, indeno quinolines, and phenanthridines. Synlett 2001, 2, 240.
-
(2001)
Synlett
, vol.2
, pp. 240
-
-
Yadav, J.S.1
Subba Reddy, B.V.2
Srinivas, R.3
Madhuri, C.H.4
Ramalingam, T.5
-
33
-
-
0001595120
-
Role reversal in the cyclocondensation of cyclo- pentadiene with heterodienophiles derived from aryl amines and aldehydes: Synthesis of novel tetrahydroquinolines
-
(a) Grieco, P. A.; Bahsas, A. Role reversal in the cyclocondensation of cyclo- pentadiene with heterodienophiles derived from aryl amines and aldehydes: Synthesis of novel tetrahydroquinolines. Tetrahedron Lett. 1988, 29, 5855
-
(1988)
Tetrahedron Lett
, vol.29
, pp. 5855
-
-
Grieco, P.A.1
Bahsas, A.2
-
34
-
-
0026068030
-
Synthesis of tetrahydroquino- lines from aromatic amines, formaldehyde, and electron rich alkenes: Evidence for nonconcertedness
-
(b) Mellor, J. M.; Merriman, G. D.; Rivere, P. Synthesis of tetrahydroquino- lines from aromatic amines, formaldehyde, and electron rich alkenes: Evidence for nonconcertedness. Tetrahedron Lett. 1991, 32, 7103.
-
(1991)
Tetrahedron Lett
, vol.32
, pp. 7103
-
-
Mellor, J.M.1
Merriman, G.D.2
Rivere, P.3
-
35
-
-
84932245583
-
-
Jon, T.; Hagihara, N. Reaction of Schiff bases with alkyl vinyl ethers catalyzed by Co2(CO)8 or Ni(CO)4. Nippon Kagaku Zashi 1970, 91, 378; Chem. Abstr. 1970, 73, 45294.
-
Jon, T.; Hagihara, N. Reaction of Schiff bases with alkyl vinyl ethers catalyzed by Co2(CO)8 or Ni(CO)4. Nippon Kagaku Zashi 1970, 91, 378; Chem. Abstr. 1970, 73, 45294.
-
-
-
-
36
-
-
0000249352
-
Schizoid activity of N-benzylidene: Aniline toward clay-catalyzed cycloadditions
-
Cabral, J.; Laszlo, P.; Montaufier, M. T. Schizoid activity of N-benzylidene: Aniline toward clay-catalyzed cycloadditions. Tetrahedron Lett. 1988, 29, 547.
-
(1988)
Tetrahedron Lett
, vol.29
, pp. 547
-
-
Cabral, J.1
Laszlo, P.2
Montaufier, M.T.3
-
37
-
-
0037421092
-
Aza-Diels-Alder reaction in fluorinated alcohols: A one-pot synthesis of tetrahydroquinolines
-
Spanedda, M. V.; Hoang, V. D.; Crousse, B.; Bonnet-Delpon, D.; Begue, J. P. Aza-Diels-Alder reaction in fluorinated alcohols: A one-pot synthesis of tetrahydroquinolines. Tetrahedron Lett. 2003, 44, 217.
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 217
-
-
Spanedda, M.V.1
Hoang, V.D.2
Crousse, B.3
Bonnet-Delpon, D.4
Begue, J.P.5
-
38
-
-
25444530933
-
Molecular iodine-catalyzed imino-Diels-Alder reactions: Efficient one-pot synthesis of pyrano[3,2-c] quinolines
-
Xia, M.; Lu, Y. Molecular iodine-catalyzed imino-Diels-Alder reactions: Efficient one-pot synthesis of pyrano[3,2-c] quinolines. Synlett 2005, 2357.
-
(2005)
Synlett
, pp. 2357
-
-
Xia, M.1
Lu, Y.2
-
39
-
-
33745431146
-
TMSCl-catalyzed aza-Diels-Alder reaction: A simple and efficient synthesis of pyrano- and furanoquinolines
-
More, S. V.; Sastry, M. N. V.; Yao, C. TMSCl-catalyzed aza-Diels-Alder reaction: A simple and efficient synthesis of pyrano- and furanoquinolines. Synlett 2006, 1399.
-
(2006)
Synlett
, pp. 1399
-
-
More, S.V.1
Sastry, M.N.V.2
Yao, C.3
-
40
-
-
34248386529
-
CAN-Catalyzed vinylogous povarov reaction: The first three-component synthesis of2-functionalized tet- rahydroquinolines from anilines, cinnamaldehyde and vinyl ethers
-
(a) Sridharan, V.; Avendano, C.; Menendez, J. C. CAN-Catalyzed vinylogous povarov reaction: The first three-component synthesis of2-functionalized tet- rahydroquinolines from anilines, cinnamaldehyde and vinyl ethers. Synlett 2007, 1079
-
(2007)
Synlett
, pp. 1079
-
-
Sridharan, V.1
Avendano, C.2
Menendez, J.C.3
-
41
-
-
34247587011
-
-
(b) Sridharan, V.; Perumal, P. T.; Avendafio, C.; Menendez, J. C.; Org. Biomol. Chem. 2007, 5, 1351.
-
(2007)
Org. Biomol. Chem
, vol.5
, pp. 1351
-
-
Sridharan, V.1
Perumal, P.T.2
Avendafio, C.3
Menendez, J.C.4
-
42
-
-
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.
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 7569
-
-
Powell, D.A.1
Batey, R.A.2
-
43
-
-
67650215788
-
Miler and related syntheses, see: Jones, G
-
For a general review of, Weissberger, A, Taylor, E. C, Eds, Wiley, and reference cited therein
-
For a general review of Doebner-von Miler and related syntheses, see: Jones, G. In The Chemistry of Heterocyclic Compounds; Weissberger, A.; Taylor, E. C., Eds.; Wiley, 1977; Vol. 32, pp. 93-318 and reference cited therein.
-
(1977)
The Chemistry of Heterocyclic Compounds
, vol.32
, pp. 93-318
-
-
Doebner-von1
-
44
-
-
37049079926
-
Stereochemistry of the tetrahydroquinolines from the condensation of methylaniline and glyco- laldehyde
-
(a) Turner, A. B.; McBain, B. I.; Howie, R. A.; Cox, P. J. Stereochemistry of the tetrahydroquinolines from the condensation of methylaniline and glyco- laldehyde. J. Chem. Soc., Perkin Trans. 1 1986, 1151-1155
-
(1986)
J. Chem. Soc., Perkin Trans. 1
, pp. 1151-1155
-
-
Turner, A.B.1
McBain, B.I.2
Howie, R.A.3
Cox, P.J.4
-
45
-
-
0011984883
-
-
and references cited therein
-
(b) Westerwelle, U.; Keuper, R.; Risch, N. J. Org. Chem. 1995, 60, 2263-2266 and references cited therein.
-
(1995)
J. Org. Chem
, vol.60
, pp. 2263-2266
-
-
Westerwelle, U.1
Keuper, R.2
Risch, N.3
-
46
-
-
0034685750
-
-
Using benzotriazole catalysts: (a) Talukdar, S, Chen, C.-T, Fang, J.-M. A steroselective route to polysubstituted terahydroquinolines by bezotriazole promoted condensation of aliphatic aldehydes and aromatic amines. J. Org. Chem. 2000, 65, 3148-3153
-
Using benzotriazole catalysts: (a) Talukdar, S.; Chen, C.-T.; Fang, J.-M. A steroselective route to polysubstituted terahydroquinolines by bezotriazole promoted condensation of aliphatic aldehydes and aromatic amines. J. Org. Chem. 2000, 65, 3148-3153
-
-
-
-
47
-
-
0028875774
-
-
Katritzky, A. R.; Rachwal, B.; Rachwal, S. A versatile method for the preparation of substituted 1,2,3,4-tetrahydroquino- lines. J. Org. Chem. 1995, 60, 7631-7640.
-
(b) Katritzky, A. R.; Rachwal, B.; Rachwal, S. A versatile method for the preparation of substituted 1,2,3,4-tetrahydroquino- lines. J. Org. Chem. 1995, 60, 7631-7640.
-
-
-
|