-
1
-
-
84944031181
-
-
Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds), Pergamon, Oxford Chapter 5.06
-
Balasubramanian M., and Keay J.G. In: Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds). Comprehensive Heterocyclic Chemistry II Vol. 5 (1996), Pergamon, Oxford 245 Chapter 5.06
-
(1996)
Comprehensive Heterocyclic Chemistry II
, vol.5
, pp. 245
-
-
Balasubramanian, M.1
Keay, J.G.2
-
2
-
-
33750428285
-
-
Jones G. (Ed), John Wiley and Sons, Chichester, UK Part 2
-
Claret P.A., and Osborne A.G. In: Jones G. (Ed). The Chemistry of Heterocyclic Compounds; Quinolines Vol. 32 (1982), John Wiley and Sons, Chichester, UK 31-32 Part 2
-
(1982)
The Chemistry of Heterocyclic Compounds; Quinolines
, vol.32
, pp. 31-32
-
-
Claret, P.A.1
Osborne, A.G.2
-
3
-
-
45449093584
-
-
Daines, R. A.; Kingsbury, W. D.; Pendrak, I.; Mallamo, J. P. Quinoline- and Naphthalenecarboxamides, Pharmaceutical Compositions and Methods of Inhibiting Calpain. U.S. Patent Application U.S. 6,100,267, August 8, 2000.
-
Daines, R. A.; Kingsbury, W. D.; Pendrak, I.; Mallamo, J. P. Quinoline- and Naphthalenecarboxamides, Pharmaceutical Compositions and Methods of Inhibiting Calpain. U.S. Patent Application U.S. 6,100,267, August 8, 2000.
-
-
-
-
4
-
-
15244355255
-
-
and references cited therein
-
Martínez-Grueiro M., Giménez-Pardo C., Gómez-Barrio A., Franck X., Fournet A., Hocquemiller R., Figadère B., and Casado-Escribano N. IL Farmaco 60 (2005) 219 and references cited therein
-
(2005)
IL Farmaco
, vol.60
, pp. 219
-
-
Martínez-Grueiro, M.1
Giménez-Pardo, C.2
Gómez-Barrio, A.3
Franck, X.4
Fournet, A.5
Hocquemiller, R.6
Figadère, B.7
Casado-Escribano, N.8
-
5
-
-
0027447599
-
-
Fournet A., Barrios A.A., Munoz V., Hocquemiller R., Cave A., and Bruneton J. Antimicrob. Agents Chemother. 37 (1993) 859
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 859
-
-
Fournet, A.1
Barrios, A.A.2
Munoz, V.3
Hocquemiller, R.4
Cave, A.5
Bruneton, J.6
-
7
-
-
0242266523
-
-
Fakhfakh M.A., Fournet A., Prina E., Mouscadet J.-F., Franck X., Hocquemiller R., and Figadère B. Bioorg. Med. Chem. 11 (2003) 5013
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 5013
-
-
Fakhfakh, M.A.1
Fournet, A.2
Prina, E.3
Mouscadet, J.-F.4
Franck, X.5
Hocquemiller, R.6
Figadère, B.7
-
8
-
-
0037430658
-
-
Fournet A., Mahieux R., Fakhfakh M.A., Franck X., Hocquemiller R., and Figadère B. Bioorg. Med. Chem. Lett. 13 (2003) 891
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 891
-
-
Fournet, A.1
Mahieux, R.2
Fakhfakh, M.A.3
Franck, X.4
Hocquemiller, R.5
Figadère, B.6
-
9
-
-
0035806298
-
-
Fakhfakh M.A., Franck X., Fournet A., Hocquemiller R., and Figadère B. Tetrahedron Lett. 42 (2001) 3847
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 3847
-
-
Fakhfakh, M.A.1
Franck, X.2
Fournet, A.3
Hocquemiller, R.4
Figadère, B.5
-
11
-
-
0036038489
-
-
Fakhfakh M.A., Franck X., Fournet A., Hocquemiller R., and Figadère B. Synth. Commun. 32 (2002) 2863
-
(2002)
Synth. Commun.
, vol.32
, pp. 2863
-
-
Fakhfakh, M.A.1
Franck, X.2
Fournet, A.3
Hocquemiller, R.4
Figadère, B.5
-
17
-
-
1242271375
-
-
Seck M., Franck X., Hocquemiller R., Figadère B., Peyrat J.-F., Provot O., Brion J.-D., and Alami M. Tetrahedron Lett. 45 (2004) 1881
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 1881
-
-
Seck, M.1
Franck, X.2
Hocquemiller, R.3
Figadère, B.4
Peyrat, J.-F.5
Provot, O.6
Brion, J.-D.7
Alami, M.8
-
23
-
-
3442888245
-
-
For the synthesis of 6-alkynylquinolines, see:
-
For the synthesis of 6-alkynylquinolines, see:. Beletskaya I.P., Latyshev G.V., Tsvetkov A.V., and Lukashev N.V. Russ. Chem. Bull., Int. Ed. 53 (2004) 189
-
(2004)
Russ. Chem. Bull., Int. Ed.
, vol.53
, pp. 189
-
-
Beletskaya, I.P.1
Latyshev, G.V.2
Tsvetkov, A.V.3
Lukashev, N.V.4
-
24
-
-
36148965545
-
-
Bera R., Swamy N.K., Dhananjaya G., Babu J.M., Kumar P.R., Mukkanti K., and Pal M. Tetrahedron 63 (2007) 13018
-
(2007)
Tetrahedron
, vol.63
, pp. 13018
-
-
Bera, R.1
Swamy, N.K.2
Dhananjaya, G.3
Babu, J.M.4
Kumar, P.R.5
Mukkanti, K.6
Pal, M.7
-
26
-
-
45449101529
-
-
See also:
-
See also:
-
-
-
-
27
-
-
45449110419
-
-
Kalleda, S.; Padakanti, S.; Kumara Swamy, N.; Yeleswarapu, K. R.; Alexander, C. W.; Khanna, I. K.; Iqbal, J.; Pillarisetti, S.; Pal, M.; Barange, D. Novel Pyrimidine Compounds, Process for their Preparation and Compositions Containing them. World Patent Application WO 2006034473 A2, March 30, 2006.
-
Kalleda, S.; Padakanti, S.; Kumara Swamy, N.; Yeleswarapu, K. R.; Alexander, C. W.; Khanna, I. K.; Iqbal, J.; Pillarisetti, S.; Pal, M.; Barange, D. Novel Pyrimidine Compounds, Process for their Preparation and Compositions Containing them. World Patent Application WO 2006034473 A2, March 30, 2006.
-
-
-
-
28
-
-
33750698953
-
-
Raju S., Kumar P.R., Mukkanti K., Annamalai P., and Pal M. Bioorg. Med. Chem. Lett. 16 (2006) 6185
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 6185
-
-
Raju, S.1
Kumar, P.R.2
Mukkanti, K.3
Annamalai, P.4
Pal, M.5
-
29
-
-
24344437318
-
-
Batchu V.R., Subramanian V., Parasuraman K., Swamy N.K., Kumar S., and Pal M. Tetrahedron 61 (2005) 9869
-
(2005)
Tetrahedron
, vol.61
, pp. 9869
-
-
Batchu, V.R.1
Subramanian, V.2
Parasuraman, K.3
Swamy, N.K.4
Kumar, S.5
Pal, M.6
-
30
-
-
45449119117
-
-
See also:
-
See also:
-
-
-
-
33
-
-
45449095710
-
-
Pal, M.; Khanna, I.; Venkataraman, S.; Srinivas, P.; Sivram, P. Heterocyclic and Bicyclic Compounds, Compositions and Methods. World Patent Application WO 2006058201, June 1, 2006.
-
Pal, M.; Khanna, I.; Venkataraman, S.; Srinivas, P.; Sivram, P. Heterocyclic and Bicyclic Compounds, Compositions and Methods. World Patent Application WO 2006058201, June 1, 2006.
-
-
-
-
34
-
-
36549018663
-
-
Bera R., Dhananjaya G., Singh S.N., Ramu B., Kiran S.U., Kumar P.R., Mukkanti K., and Pal M. Tetrahedron 64 (2008) 582
-
(2008)
Tetrahedron
, vol.64
, pp. 582
-
-
Bera, R.1
Dhananjaya, G.2
Singh, S.N.3
Ramu, B.4
Kiran, S.U.5
Kumar, P.R.6
Mukkanti, K.7
Pal, M.8
-
35
-
-
45449110977
-
-
Based on experimental observations it has been suggested that coordination of quinoline nitrogen to the palladium controls the coupling reaction at the C-2 position of the quinoline ring, see:
-
Based on experimental observations it has been suggested that coordination of quinoline nitrogen to the palladium controls the coupling reaction at the C-2 position of the quinoline ring, see:
-
-
-
-
39
-
-
0023805195
-
-
Nasr M., Drach J.C., Smith S.H., Shipman Jr. C.H., and Burckhalter J.H. J. Med. Chem. 31 (1988) 1347
-
(1988)
J. Med. Chem.
, vol.31
, pp. 1347
-
-
Nasr, M.1
Drach, J.C.2
Smith, S.H.3
Shipman Jr., C.H.4
Burckhalter, J.H.5
-
40
-
-
0020034429
-
-
Kaneko C., Naito T., Momose Y., Fujii H., Nakayama N., and Koizumi I. Chem. Pharm. Bull. 30 (1982) 519
-
(1982)
Chem. Pharm. Bull.
, vol.30
, pp. 519
-
-
Kaneko, C.1
Naito, T.2
Momose, Y.3
Fujii, H.4
Nakayama, N.5
Koizumi, I.6
-
41
-
-
0037016917
-
-
For nucleophilic substitution reaction under microwave irradiation, see:
-
For nucleophilic substitution reaction under microwave irradiation, see:. Cheng Y.-J. Tetrahedron 58 (2002) 1125
-
(2002)
Tetrahedron
, vol.58
, pp. 1125
-
-
Cheng, Y.-J.1
-
42
-
-
45449116519
-
-
See Ref. 9a;
-
See Ref. 9a;
-
-
-
-
43
-
-
0030792219
-
-
Fang F.G., Bankston D.D., Huie E.M., Johnson M.R., Kang M.C., LeHoullier C.S., Lewis G.C., Lovelace T.C., Lowery M.W., McDougald D.L., Meerholz C.A., Partridge J.J., Sharp M.J., and Xie S. Tetrahedron 53 (1997) 10953
-
(1997)
Tetrahedron
, vol.53
, pp. 10953
-
-
Fang, F.G.1
Bankston, D.D.2
Huie, E.M.3
Johnson, M.R.4
Kang, M.C.5
LeHoullier, C.S.6
Lewis, G.C.7
Lovelace, T.C.8
Lowery, M.W.9
McDougald, D.L.10
Meerholz, C.A.11
Partridge, J.J.12
Sharp, M.J.13
Xie, S.14
-
48
-
-
0033549049
-
-
Aranyos A., Old D.W., Kiyomori A., Wolfe J.P., Sadighi J.P., and Buchwald S.L. J. Am. Chem. Soc. 121 (1999) 4369
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 4369
-
-
Aranyos, A.1
Old, D.W.2
Kiyomori, A.3
Wolfe, J.P.4
Sadighi, J.P.5
Buchwald, S.L.6
-
49
-
-
0000157513
-
-
For a review on C-O bond formation under Pd-catalysis, see:
-
For a review on C-O bond formation under Pd-catalysis, see:. Muci A.R., and Buchwald S.L. Top. Curr. Chem. 219 (2002) 131
-
(2002)
Top. Curr. Chem.
, vol.219
, pp. 131
-
-
Muci, A.R.1
Buchwald, S.L.2
-
50
-
-
0348167677
-
-
2,4-Dichloroquinoline was prepared via the reaction of aniline with malonic acid in an excess of phosphorus oxychloride at reflux, see:
-
2,4-Dichloroquinoline was prepared via the reaction of aniline with malonic acid in an excess of phosphorus oxychloride at reflux, see:. Jones K., Roset X., Rossiter S., and Whitfield P. Org. Biomol. Chem. 1 (2003) 4380
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 4380
-
-
Jones, K.1
Roset, X.2
Rossiter, S.3
Whitfield, P.4
-
52
-
-
0042331953
-
-
Huang C.Q., Wilcoxen K., McCarthy J.R., Haddach M., Webb T.R., Gu J., Xie Y.-F., Grigoriadis D.E., and Chen C. Bioorg. Med. Chem. Lett. 13 (2003) 3375
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3375
-
-
Huang, C.Q.1
Wilcoxen, K.2
McCarthy, J.R.3
Haddach, M.4
Webb, T.R.5
Gu, J.6
Xie, Y.-F.7
Grigoriadis, D.E.8
Chen, C.9
-
53
-
-
33644556178
-
-
Zhong B., Al-Awar R.S., Shih C., Grimes Jr. J.H., Vieth M., and Hamdouchi C. Tetrahedron Lett. 47 (2006) 2161
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 2161
-
-
Zhong, B.1
Al-Awar, R.S.2
Shih, C.3
Grimes Jr., J.H.4
Vieth, M.5
Hamdouchi, C.6
-
55
-
-
45449110602
-
-
Allgeier, H.; Auberson, Y.; Biollaz, M.; Cosford, N. D.; Gasparini, F.; Heckendorn, R.; Johnson, E. C.; Kuhn, R.; Varney, M. A.; Velicelebi, G. Preparation of Pyridine Derivatives for Treating Disorders Mediated Full or in Part by mGluR5. World Patent Application Appl. WO 9902497 A2, 1999.
-
Allgeier, H.; Auberson, Y.; Biollaz, M.; Cosford, N. D.; Gasparini, F.; Heckendorn, R.; Johnson, E. C.; Kuhn, R.; Varney, M. A.; Velicelebi, G. Preparation of Pyridine Derivatives for Treating Disorders Mediated Full or in Part by mGluR5. World Patent Application Appl. WO 9902497 A2, 1999.
-
-
-
-
61
-
-
2942744717
-
-
Elangovan A., Yang S.-W., Lin J.-H., Kao K.-M., and Ho T.-I. Org. Biomol. Chem. 2 (2004) 1597
-
(2004)
Org. Biomol. Chem.
, vol.2
, pp. 1597
-
-
Elangovan, A.1
Yang, S.-W.2
Lin, J.-H.3
Kao, K.-M.4
Ho, T.-I.5
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