-
1
-
-
0035811449
-
Synthesis and antibacterial evaluation of certain quinolone derivatives
-
1:CAS:528:DC%2BD3MXktFalsbg%3D 11428933 10.1021/jm0100335
-
Chen YL, Fang KC, Sheu JY, Hsu SL, Tzeng SS (2001) Synthesis and antibacterial evaluation of certain quinolone derivatives. J Med Chem 44:2374-2377
-
(2001)
J Med Chem
, vol.44
, pp. 2374-2377
-
-
Chen, Y.L.1
Fang, K.C.2
Sheu, J.Y.3
Hsu, S.L.4
Tzeng, S.S.5
-
2
-
-
39749084608
-
Structure-activity relationship of coumarin derivatives on xanthine oxidase-inhibiting and free radical-scavenging activities
-
1:CAS:528:DC%2BD1cXislamtbk%3D 18201686 10.1016/j.bcp.2007.11.023
-
Lin HC, Tsai SH, Chen CS, Chang YC, Lee CM, Lai ZY, Lin CM (2008) Structure-activity relationship of coumarin derivatives on xanthine oxidase-inhibiting and free radical-scavenging activities. Biochem Pharmacol 75:1416-1425
-
(2008)
Biochem Pharmacol
, vol.75
, pp. 1416-1425
-
-
Lin, H.C.1
Tsai, S.H.2
Chen, C.S.3
Chang, Y.C.4
Lee, C.M.5
Lai, Z.Y.6
Lin, C.M.7
-
3
-
-
41749084640
-
Chemical library and structure-activity relationships of 11-demethyl-12-oxo calanolide a analogues as anti-HIV-1 agents
-
1:CAS:528:DC%2BD1cXitFeht7g%3D 18284187 10.1021/jm701405p
-
Ma T, Liu L, Xue H, Li L, Han C, Wang L, Chen Z, Liu G (2008) Chemical library and structure-activity relationships of 11-demethyl-12-oxo calanolide a analogues as anti-HIV-1 agents. J Med Chem 51:1432-1446
-
(2008)
J Med Chem
, vol.51
, pp. 1432-1446
-
-
Ma, T.1
Liu, L.2
Xue, H.3
Li, L.4
Han, C.5
Wang, L.6
Chen, Z.7
Liu, G.8
-
4
-
-
0037971925
-
Novel coumarin derivatives of heterocyclic compounds as lipid-lowering agents
-
1:CAS:528:DC%2BD3sXlt1WgsbY%3D 12852963 10.1016/S0960-894X(03)00490-6
-
Madhavan GR, Balraju V, Mallesham B, Chakrabarthi R, Lohray VB (2003) Novel coumarin derivatives of heterocyclic compounds as lipid-lowering agents. Bioorg Med Chem Lett 13:2547-2551
-
(2003)
Bioorg Med Chem Lett
, vol.13
, pp. 2547-2551
-
-
Madhavan, G.R.1
Balraju, V.2
Mallesham, B.3
Chakrabarthi, R.4
Lohray, V.B.5
-
5
-
-
0028217675
-
Short synthesis of the dynemicin core structure: Unusual bridgehead enolate reactivity
-
10.1039/c39940001543
-
Magnus P, Parry D, Illiadis T, Eisenbeis SA, Fairhuist RA (1994) Short synthesis of the dynemicin core structure: unusual bridgehead enolate reactivity. J Chem Soc Chem Commun 13:1543-1544
-
(1994)
J Chem Soc Chem Commun
, vol.13
, pp. 1543-1544
-
-
Magnus, P.1
Parry, D.2
Illiadis, T.3
Eisenbeis, S.A.4
Fairhuist, R.A.5
-
6
-
-
0030047733
-
Total synthesis of (-)-tetrahydropalmatine via chiral formamidine carbanions:unexpected behavior with certain ortho-substituted electrophiles
-
1:CAS:528:DyaK28Xis1Krsw%3D%3D 11666977 10.1021/jo951611q
-
Matulenko MA, Meyers AI (1996) Total synthesis of (-)-tetrahydropalmatine via chiral formamidine carbanions:unexpected behavior with certain ortho-substituted electrophiles. J Org Chem 61:573-580
-
(1996)
J Org Chem
, vol.61
, pp. 573-580
-
-
Matulenko, M.A.1
Meyers, A.I.2
-
7
-
-
0023087057
-
Substituted arylmethyl phenyl ethers. 1. A novel series of 5-lipoxygenase inhibitors and leukotriene antagonists
-
1:CAS:528:DyaL2sXhsl2quw%3D%3D 3806607 10.1021/jm00384a017
-
Musser JH, Chakraborty UR, Sciortino S, Gordon RJ, Khandwala A, Neiss ES, Pruss TP, Van Inwegen RG, Weinryb I, Coutts SM (1987) Substituted arylmethyl phenyl ethers. 1. A novel series of 5-lipoxygenase inhibitors and leukotriene antagonists. J Med Chem 30:96-104
-
(1987)
J Med Chem
, vol.30
, pp. 96-104
-
-
Musser, J.H.1
Chakraborty, U.R.2
Sciortino, S.3
Gordon, R.J.4
Khandwala, A.5
Neiss, E.S.6
Pruss, T.P.7
Van Inwegen, R.G.8
Weinryb, I.9
Coutts, S.M.10
-
8
-
-
47749108003
-
Synthesis of a new class of bisheterocycles from phenacylsulfonylacetic acid methyl ester
-
1:CAS:528:DC%2BD1cXoslymt74%3D 10.1002/jhet.5570450430
-
Padmavathi V, Mohan AVN, Mahesh K (2008) Synthesis of a new class of bisheterocycles from phenacylsulfonylacetic acid methyl ester. J Heterocycl Chem 45:1131-1138
-
(2008)
J Heterocycl Chem
, vol.45
, pp. 1131-1138
-
-
Padmavathi, V.1
Mohan, A.V.N.2
Mahesh, K.3
-
9
-
-
0032900708
-
A cycloaddition approach toward the synthesis of substituted indolines and tetrahydroquinolines
-
1:CAS:528:DyaK1MXivFyltbw%3D 11674487 10.1021/jo982453g
-
Padwa A, Brodney MA, Liu B, Satake K, Wu T (1999) A cycloaddition approach toward the synthesis of substituted indolines and tetrahydroquinolines. J Org Chem 64:3595-3607
-
(1999)
J Org Chem
, vol.64
, pp. 3595-3607
-
-
Padwa, A.1
Brodney, M.A.2
Liu, B.3
Satake, K.4
Wu, T.5
-
10
-
-
84856641119
-
Camphorsulfonic acid catalysed facile tandem double Friedlander annulation protocol for the synthesis of phenoxy linked bisquinoline derivatives and discovery of antitubercular agents
-
1:CAS:528:DC%2BC38XitVWrt7Y%3D 22277278 10.1016/j.bmcl.2011.12.119
-
Paul N, Murugavel M, Muthusubramanian S, Sriram D (2012) Camphorsulfonic acid catalysed facile tandem double Friedlander annulation protocol for the synthesis of phenoxy linked bisquinoline derivatives and discovery of antitubercular agents. Bioorg Med Chem Lett 22:1643-1648
-
(2012)
Bioorg Med Chem Lett
, vol.22
, pp. 1643-1648
-
-
Paul, N.1
Murugavel, M.2
Muthusubramanian, S.3
Sriram, D.4
-
11
-
-
77958067742
-
Synthesis and antihyperlipidemic activity of novel coumarin bisindole derivatives
-
1:CAS:528:DC%2BC3cXhtlSms7bJ 20932744 10.1016/j.bmcl.2010.09.055
-
Sashidhara KV, Kumar A, Kumar M, Srivastava A, Puri A (2010) Synthesis and antihyperlipidemic activity of novel coumarin bisindole derivatives. Bioorg Med Chem Lett 20:6504-6507
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 6504-6507
-
-
Sashidhara, K.V.1
Kumar, A.2
Kumar, M.3
Srivastava, A.4
Puri, A.5
-
12
-
-
33846458645
-
Synthesis and antimalarial activity of side chain modified 4-aminoquinoline derivatives
-
1:CAS:528:DC%2BD28XhtlKjsrvL 17228883 10.1021/jm061002i
-
Solomon VR, Haq W, Srivastava K, Puri SK, Katti SB (2007) Synthesis and antimalarial activity of side chain modified 4-aminoquinoline derivatives. J Med Chem 50:394-398
-
(2007)
J Med Chem
, vol.50
, pp. 394-398
-
-
Solomon, V.R.1
Haq, W.2
Srivastava, K.3
Puri, S.K.4
Katti, S.B.5
-
13
-
-
70349270651
-
Practical synthesis of maleimides and coumarin-linked probes for protein and anti body labelling via reduction of native disulfides
-
1:CAS:528:DC%2BD1MXpsl2itrw%3D 19675893 10.1039/b904060a
-
Song HY, Ngai MH, Song ZY, MacAry PA, Hobley J, Lear MJ (2009) Practical synthesis of maleimides and coumarin-linked probes for protein and anti body labelling via reduction of native disulfides. Org Biomol Chem 7:3400-3406
-
(2009)
Org Biomol Chem
, vol.7
, pp. 3400-3406
-
-
Song, H.Y.1
Ngai, M.H.2
Song, Z.Y.3
Macary, P.A.4
Hobley, J.5
Lear, M.J.6
-
14
-
-
33845374421
-
Thioaldehyde Diels-Alder reactions
-
1:CAS:528:DyaL28XitVOisro%3D 10.1021/jo00359a034
-
Vedejs E, Eberlein TH, Mazur DJ, McClure CK, Perry DA, Ruggeri R, Schwartz E, Stults JS, Varie DL (1986) Thioaldehyde Diels-Alder reactions. J Org Chem 51:1556-1562
-
(1986)
J Org Chem
, vol.51
, pp. 1556-1562
-
-
Vedejs, E.1
Eberlein, T.H.2
Mazur, D.J.3
McClure, C.K.4
Perry, D.A.5
Ruggeri, R.6
Schwartz, E.7
Stults, J.S.8
Varie, D.L.9
-
15
-
-
27944434132
-
Design, synthesis, and vasorelaxant and platelet antiaggregatory activities of coumarin-resveratrol hybrids
-
1:CAS:528:DC%2BD2MXht1Git7bN 16275073 10.1016/j.bmcl.2005.10.013
-
Vilar S, Quezada E, Santana L, Uriarte E, Yanez M, Fraiz N, Alcalde C, Cano E, Orallo F (2006) Design, synthesis, and vasorelaxant and platelet antiaggregatory activities of coumarin-resveratrol hybrids. Bioorg Med Chem Lett 16:257-261
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 257-261
-
-
Vilar, S.1
Quezada, E.2
Santana, L.3
Uriarte, E.4
Yanez, M.5
Fraiz, N.6
Alcalde, C.7
Cano, E.8
Orallo, F.9
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