-
1
-
-
0027257652
-
Selective non-nucleoside HIV-1 reverse transcriptase inhibitors. New 2,3-dihydrothiazolo[2,3-a]isoindol-5(9bH)-ones and related compounds with anti-HIV-1 activity
-
(a) Mertens, A.; Zilch, H.; Koenig, B.; Schaefer, W.; Poll, T.; Kampe, W.; Seidel, H.; Leser, U.; Leinert, H. Selective non-nucleoside HIV-1 reverse transcriptase inhibitors. New 2,3- dihydrothiazolo[2,3-a]isoindol-5(9bH)-ones and related compounds with anti-HIV-1 activity. J. Med. Chem. 1993, 36, 2526;
-
(1993)
J. Med. Chem.
, vol.36
, pp. 2526
-
-
Mertens, A.1
Zilch, H.2
Koenig, B.3
Schaefer, W.4
Poll, T.5
Kampe, W.6
Seidel, H.7
Leser, U.8
Leinert, H.9
-
3
-
-
0034699382
-
A chemical switch for inhibitor-sensitive alleles of any protein kinase
-
(c) Bishop, A. C.; Ubersax, J. A.; Shokat, K. M. A chemical switch for inhibitor-sensitive alleles of any protein kinase. Nature 2000, 407, 395;
-
(2000)
Nature
, vol.407
, pp. 395
-
-
Bishop, A.C.1
Ubersax, J.A.2
Shokat, K.M.3
-
4
-
-
0036549654
-
Synthesis and SAR studies for the inhibition of TNF-alpha production. Part 2. 2-[3-(Cyclopentyloxy)-4-methoxyphenyl]- substituted-1-isoindolinone derivatives
-
(d) Park, J. S.; Moon, S. C.; Baik, K. U.; Cho, J. Y.; Yoo, E. S.; Byun, Y. S.; Park, M. H. Synthesis and SAR studies for the inhibition of TNF-alpha production. Part 2. 2-[3-(Cyclopentyloxy)-4-methoxyphenyl]- substituted-1- isoindolinone derivatives. Arch. Pharm. Res. 2002, 25, 137;
-
(2002)
Arch. Pharm. Res.
, vol.25
, pp. 137
-
-
Park, J.S.1
Moon, S.C.2
Baik, K.U.3
Cho, J.Y.4
Yoo, E.S.5
Byun, Y.S.6
Park, M.H.7
-
5
-
-
34547592204
-
Design synthesis, and evaluation of isoindolinone-hydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors
-
(e) Lee, S.; Shinji, C.; Ogura, K.; Shimizu, M.; Maeda, S.; Sato, M.; Yoshida, M.; Hashimoto, Y.; Miyachi, H. Design, synthesis, and evaluation of isoindolinone-hydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors. Bioorg. Med. Chem. Lett. 2007, 17, 4895;
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 4895
-
-
Lee, S.1
Shinji, C.2
Ogura, K.3
Shimizu, M.4
Maeda, S.5
Sato, M.6
Yoshida, M.7
Hashimoto, Y.8
Miyachi, H.9
-
6
-
-
36849081787
-
Novel water-soluble sedative-hypnotic agents: Isoindolin-1-one derivatives
-
(f) Kanamitsu, N.; Osaki, T.; Itsuji, Y.; Yoshimura, M.; Tsujimoto, H.; Soga, M. Novel water-soluble sedative-hypnotic agents: Isoindolin-1-one derivatives. Chem. Pharm. Bull. 2007, 55, 1682;
-
(2007)
Chem. Pharm. Bull.
, vol.55
, pp. 1682
-
-
Kanamitsu, N.1
Osaki, T.2
Itsuji, Y.3
Yoshimura, M.4
Tsujimoto, H.5
Soga, M.6
-
7
-
-
51549112706
-
7-[1H-Indol-2- yl]-2,3-dihydro-isoindol-1-ones as dual Aurora-A/VEGF-R2 kinase inhibitors: Design, synthesis, and biological activity
-
(g) Hughes, T. V.; Emanuel, S. L.; O'Grady, H. R.; Connolly, P. J.; Rugg, C.; Fuentes-Pesquera, A. R.; Karnachi, P.; Alexander, R.; Middleton, S. A. 7-[1H-Indol-2- yl]-2,3-dihydro-isoindol-1-ones as dual Aurora-A/VEGF-R2 kinase inhibitors: Design, synthesis, and biological activity. Bioorg. Med. Chem. Lett. 2008, 18, 5130;
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 5130
-
-
Hughes, T.V.1
Emanuel, S.L.2
O'grady, H.R.3
Connolly, P.J.4
Rugg, C.5
Fuentes-Pesquera, A.R.6
Karnachi, P.7
Alexander, R.8
Middleton, S.A.9
-
8
-
-
38149076469
-
-
(h) Mason, K. A; Valdecanas, D.; Hunter, N. R.; Milas, L. Invest. New Drugs 2008, 26, 1.
-
(2008)
Invest. New Drugs
, vol.26
, pp. 1
-
-
Mason, K.A.1
Valdecanas, D.2
Hunter, N.R.3
Milas, L.4
-
9
-
-
0027437245
-
Stereoselective pharmacokinetics of pazinaclone, a new non-benzodiazepine anxiolytic, and its active metabolite in healthy subjects
-
(a) Hussein, Z.; Mulford, D. J.; Bopp, B. A.; Granneman, G. R. Stereoselective pharmacokinetics of pazinaclone, a new non-benzodiazepine anxiolytic, and its active metabolite in healthy subjects. Br. J. Clin. Pharmacol. 1993, 36, 357;
-
(1993)
Br. J. Clin. Pharmacol.
, vol.36
, pp. 357
-
-
Hussein, Z.1
Mulford, D.J.2
Bopp, B.A.3
Granneman, G.R.4
-
10
-
-
0034757548
-
Pagoclone. Anxiolytic GABA-A/BZD site partial agonist
-
(b) Sorbera, L. A.; Leeson, P. A.; Silvestre, J.; Castaner, J. Pagoclone. Anxiolytic, GABA-A/BZD site partial agonist. Drugs of the Future 2001, 26, 651;
-
(2001)
Drugs of the Future
, vol.26
, pp. 651
-
-
Sorbera, L.A.1
Leeson, P.A.2
Silvestre, J.3
Castaner, J.4
-
11
-
-
0034877353
-
Crossover trial of pagoclone and placebo in patients with DSM-IV panic disorder
-
(c) Sandford, J. J.; Forshall, S.; Bell, C. Crossover trial of pagoclone and placebo in patients with DSM-IV panic disorder. J. Psychopharmacol. 2001, 15, 205;
-
(2001)
J. Psychopharmacol.
, vol.15
, pp. 205
-
-
Sandford, J.J.1
Forshall, S.2
Bell, C.3
-
12
-
-
33645975532
-
2-(4-Hydroxy-biphenyl-3-yl)isoindolin-1-one
-
(d) Atack, J. R.; Pike, A.; Marshall, G. 2-(4-Hydroxy-biphenyl-3-yl) isoindolin-1-one. Neuropharmacology 2006, 50, 677.
-
(2006)
Neuropharmacology
, vol.50
, pp. 677
-
-
Atack, J.R.1
Pike, A.2
Marshall, G.3
-
13
-
-
0033371437
-
A comparative assessment of the risks and benefits of zopiclone: A review of 15 years' clinical experience
-
(a) Hajak, G. A comparative assessment of the risks and benefits of zopiclone: A review of 15 years' clinical experience. Drug Safety 1999, 21, 457;
-
(1999)
Drug Safety
, vol.21
, pp. 457
-
-
Hajak, G.1
-
14
-
-
0033109310
-
Residual effects of zolpidem 10mg and zopiclone 7.5 mg versus flunitrazepam 1mg and placebo on driving performance and ocular saccades
-
(b) Bocca, M. L.; Le Doze, F.; Etard, O.; Pottier, M.; L'Hoste, J.; Denise, P. Residual effects of zolpidem 10mg and zopiclone 7.5 mg versus flunitrazepam 1mg and placebo on driving performance and ocular saccades. Psychopharmacology 1999, 143, 373;
-
(1999)
Psychopharmacology
, vol.143
, pp. 373
-
-
Bocca, M.L.1
Le Doze, F.2
Etard, O.3
Pottier, M.4
L'hoste, J.5
Denise, P.6
-
15
-
-
0035896191
-
Sedative and anxiolytic effects of zopiclone's enantiomers and metabolite
-
(c) Carlson, J. N.; Haskew, R.; Wacker, J. Sedative and anxiolytic effects of zopiclone's enantiomers and metabolite. Eur. J. Pharmacol. 2001, 415, 181;
-
(2001)
Eur. J. Pharmacol.
, vol.415
, pp. 181
-
-
Carlson, J.N.1
Haskew, R.2
Wacker, J.3
-
16
-
-
0142073864
-
Eszopiclone
-
(d) Culy, C.; Castaner, J.; Bayes, M. Eszopiclone. Drugs Future 2003, 28, 640.
-
(2003)
Drugs Future
, vol.28
, pp. 640
-
-
Culy, C.1
Castaner, J.2
Bayes, M.3
-
17
-
-
0029011730
-
Toward improved anti-HIV chemotherapy: Therapeutic strategies for intervention with HIV infections
-
(a) De Clercq, E. J. Toward improved anti-HIV chemotherapy: Therapeutic strategies for intervention with HIV infections. J. Med. Chem. 1995, 38, 2491;
-
(1995)
J. Med. Chem.
, vol.38
, pp. 2491
-
-
De Clercq, E.J.1
-
18
-
-
0030043026
-
Effect of linking bridge modifications on the antipsychotic profile of some phthalimide and isoindolinone derivatives
-
(b) Norman, M. H.; Minick, D. J.; Rigdon, G. C. Effect of linking bridge modifications on the antipsychotic profile of some phthalimide and isoindolinone derivatives. J. Med. Chem. 1996, 39, 149;
-
(1996)
J. Med. Chem.
, vol.39
, pp. 149
-
-
Norman, M.H.1
Minick, D.J.2
Rigdon, G.C.3
-
19
-
-
0031893482
-
1A receptor ligands
-
(c) Zhuang, Z. P.; Kung, M. P.; Mu, M. Hank, F. K. Isoindol-1-one analogues of 4-(2′- methoxyphenyl)-1-[2′-[N-(2″-pyridyl)-p- iodobenzamido]ethyl]piperazine (p-MPPI) as 5- HT1A receptor ligands. J. Med. Chem. 1998, 41, 157;
-
(1998)
J. Med. Chem.
, vol.41
, pp. 157
-
-
Zhuang, Z.P.1
Kung, M.P.2
Mu, M.3
Hank, F.K.4
-
20
-
-
0032537535
-
Isoindolinone enantiomers having affinity for the dopamine D4 receptor
-
(d) Belliotti, T. R.; Brink, W. A.; Wise, L. D. Isoindolinone enantiomers having affinity for the dopamine D4 receptor. Bioorg. Med. Chem. Lett. 1998, 8, 1499;
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 1499
-
-
Belliotti, T.R.1
Brink, W.A.2
Wise, L.D.3
-
21
-
-
0033598368
-
Crystallographic analysis of the binding modes of thiazoloisoindolinone non-nucleoside inhibitors to HIV-1 reverse transcriptase and comparison with modeling studies
-
(e) Ren, J. S.; Esnouf, R. M.; Hopkins, A. L.; Stuart, D. I.; Stammers, D. K. Crystallographic analysis of the binding modes of thiazoloisoindolinone non-nucleoside inhibitors to HIV-1 reverse transcriptase and comparison with modeling studies. J. Med. Chem. 1999, 42, 3845;
-
(1999)
J. Med. Chem.
, vol.42
, pp. 3845
-
-
Ren, J.S.1
Esnouf, R.M.2
Hopkins, A.L.3
Stuart, D.I.4
Stammers, D.K.5
-
22
-
-
0037157754
-
A polymersupported [1,3,2]oxazaphospholidine for the conversion of isothiocyanates to isocyanides and their subsequent use in an ugi reaction
-
(f) Ley, S. V.; Taylor, S. J. A polymersupported [1,3,2] oxazaphospholidine for the conversion of isothiocyanates to isocyanides and their subsequent use in an ugi reaction. Bioorg. Med. Chem. Lett. 2002, 12, 1813;
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1813
-
-
Ley, S.V.1
Taylor, S.J.2
-
23
-
-
13944282529
-
Isoindolinone-based inhibitors of the MDM2- p53 protein-protein interaction
-
(g) Hardcastle, I. R.; Ahmed, S. U.; Atkins, H. Isoindolinone-based inhibitors of the MDM2- p53 protein-protein interaction. Bioorg. Med. Chem. Lett. 2005, 15, 1515;
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 1515
-
-
Hardcastle, I.R.1
Ahmed, S.U.2
Atkins, H.3
-
24
-
-
33750133440
-
Small-molecule inhibitors of the MDM2-p53 protein-protein Interaction based on an isoindolinone scaffold
-
(h) Hardcastle, I. R.; Ahmed, S. U.; Atkins, H. Small-molecule inhibitors of the MDM2-p53 protein-protein Interaction based on an isoindolinone scaffold. J. Med. Chem. 2006, 49, 6209;
-
(2006)
J. Med. Chem.
, vol.49
, pp. 6209
-
-
Hardcastle, I.R.1
Ahmed, S.U.2
Atkins, H.3
-
25
-
-
34547592204
-
Design synthesis, and evaluation of isoindolinone-hydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors
-
(i) Lee, S.; Shinji, C.; Ogura, K. Design, synthesis, and evaluation of isoindolinone-hydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors. Bioorg. Med. Chem. Lett. 2007, 17, 4895.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 4895
-
-
Lee, S.1
Shinji, C.2
Ogura, K.3
-
26
-
-
0000525743
-
Addition of transientlygenerated methyl o-lithiobenzoate to imines. An isoindolone annulation
-
(a) Campbell, J. B.; Dedinas, R. F.; Trumbower-Walsh, S. A. Addition of transientlygenerated methyl o-lithiobenzoate to imines. An isoindolone annulation. J. Org. Chem. 1996, 61, 6205;
-
(1996)
J. Org. Chem.
, vol.61
, pp. 6205
-
-
Campbell, J.B.1
Dedinas, R.F.2
Trumbower-Walsh, S.A.3
-
27
-
-
0032537204
-
LDA-induced metalation of isoindolinones. An efficient route to 3-substituted isoindoline derivatives
-
(b) Couture, A.; Deniau, E.; Grandclaudon, P. LDA-induced metalation of isoindolinones. An efficient route to 3-substituted isoindoline derivatives. Tetrahedron Lett. 1998, 39, 2319;
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 2319
-
-
Couture, A.1
Deniau, E.2
Grandclaudon, P.3
-
28
-
-
0035953025
-
Synthesis of 3-alkyl-1-isoindolinones by alkylation of a benzotriazolyl substituted N-dimethylamino-phthalimidine
-
(c) Deniau, E.; Enders, D. Synthesis of 3-alkyl-1-isoindolinones by alkylation of a benzotriazolyl substituted N-dimethylamino-phthalimidine. Tetrahedron 2001, 57, 2581;
-
(2001)
Tetrahedron
, vol.57
, pp. 2581
-
-
Deniau, E.1
Enders, D.2
-
29
-
-
0037049202
-
A new synthesis of 3-alkyl-1- isoindolinones
-
(d) Wang, E. C.; Chen, H. F.; Hsu, M. K. A new synthesis of 3-alkyl-1- isoindolinones. Tetrahedron Lett. 2002, 43, 9163;
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 9163
-
-
Wang, E.C.1
Chen, H.F.2
Hsu, M.K.3
-
30
-
-
12344261806
-
Studies on the diastereoselective reductive alkylation of (R)-phenylglycinol derived phthalimide: Observation of stereoelectronic effects
-
(e) Chen, M. D.; He, M. Z.; Huang, L. Q. Studies on the diastereoselective reductive alkylation of (R)-phenylglycinol derived phthalimide: Observation of stereoelectronic effects. Tetrahedron 2005, 61, 1335.
-
(2005)
Tetrahedron
, vol.61
, pp. 1335
-
-
Chen, M.D.1
He, M.Z.2
Huang, L.Q.3
-
31
-
-
0042836595
-
Synthesis of 3-substituted isoindolin-1-ones via a palladium-catalysed 3-component carbonylation/amination/ Michael addition process
-
(a) Gai, X. J.; Grigg, R.; Khamnaen, T.; Rajviroongit, S.; Keep, A. Synthesis of 3-substituted isoindolin-1-ones via a palladium-catalysed 3-component carbonylation/amination/ Michael addition process. Tetrahedron Lett. 2003, 44, 7441;
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 7441
-
-
Gai, X.J.1
Grigg, R.2
Khamnaen, T.3
Rajviroongit, S.4
Keep, A.5
-
32
-
-
30844466406
-
Insertion of polar and nonpolar unsaturated molecules into carbon-rhenium bonds generated by C-H bond activation: Synthesis of phthalimidine and indene derivatives
-
(b) Kuninobu, Y.; Tokunaga, Y.; Kawata, Atsushi; Takai, K. Insertion of polar and nonpolar unsaturated molecules into carbon-rhenium bonds generated by C-H bond activation: Synthesis of phthalimidine and indene derivatives. J. Am. Chem. Soc. 2006, 128, 202;
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 202
-
-
Kuninobu, Y.1
Tokunaga, Y.2
Atsushi, K.3
Takai, K.4
-
33
-
-
55249103848
-
Regioselective synthesis of N-aminoisoindolones and mono-N- and di-N,N′-substituted phthalazones utilizing hydrazine nucleophiles in a palladium-catalyzed three-component cascade process
-
(c) Grigg, R.; Sridharan, V.; Shah, M. Regioselective synthesis of N-aminoisoindolones and mono-N- and di-N,N′-substituted phthalazones utilizing hydrazine nucleophiles in a palladium-catalyzed three-component cascade process. J. Org. Chem. 2008, 73, 8352.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 8352
-
-
Grigg, R.1
Sridharan, V.2
Shah, M.3
-
34
-
-
0027159663
-
Evaluation of some Mannich bases of cycloalkanones and related compounds for cytotoxic activity
-
(a) Dimmock, J. R.; Sidhu, K. K.; Chen, M.; Reid, R. S.; Allen, T. M.; Kao, G. Y.; Truitt, G. A. Evaluation of some Mannich bases of cycloalkanones and related compounds for cytotoxic activity. Eur. J. Med. Chem. 1993, 28, 313;
-
(1993)
Eur. J. Med. Chem.
, vol.28
, pp. 313
-
-
Dimmock, J.R.1
Sidhu, K.K.2
Chen, M.3
Reid, R.S.4
Allen, T.M.5
Kao, G.Y.6
Truitt, G.A.7
-
35
-
-
0029034741
-
[(Alkylamino)- methyl]acrylophenones: Potent and selective inhibitors of the epidermal growth factor receptor protein tyrosine kinase
-
(b) Traxler, P.; Trinks, U.; Buchdunger, E.; Mett, H.; Meyer, T.; Müller, M.; Regenass, U.; Rosel, J.; Lydon, N. [(Alkylamino)- methyl]acrylophenones: Potent and selective inhibitors of the epidermal growth factor receptor protein tyrosine kinase. J. Med. Chem. 1995, 38, 2441;
-
(1995)
J. Med. Chem.
, vol.38
, pp. 2441
-
-
Traxler, P.1
Trinks, U.2
Buchdunger, E.3
Mett, H.4
Meyer, T.5
Müller, M.6
Regenass, U.7
Rosel, J.8
Lydon, N.9
-
37
-
-
0000862669
-
Catalytic enantioselective addition to imines
-
(d) Kobayashi, S.; Ishitani, H. Catalytic enantioselective addition to imines. Chem. Rev. 1999, 99, 1069;
-
(1999)
Chem. Rev.
, vol.99
, pp. 1069
-
-
Kobayashi, S.1
Ishitani, H.2
-
38
-
-
0001059120
-
Alkylation of imino groups
-
Jacobsen, E. N.; Pfaltz, A.; Yamomoto, H. (Eds.); Springer: Berlin
-
(e) Denmark, S.; Nicaise, O. J. C. Alkylation of imino groups. In Comprehensive Asymmetric Catalysis. Jacobsen, E. N.; Pfaltz, A.; Yamomoto, H. (Eds.); Springer: Berlin, 1999; Vol. 2, p. 923.
-
(1999)
Comprehensive Asymmetric Catalysis
, vol.2
, pp. 923
-
-
Denmark, S.1
Nicaise, O.J.C.2
-
39
-
-
0032482080
-
Modern variants of the Mannich reaction
-
Arend, M.; Westerman, B.; Risch, N. Modern variants of the Mannich reaction. Angew. Chem., Int. Ed. 1998, 37, 1044.
-
(1998)
Angew. Chem., Int. Ed.
, vol.37
, pp. 1044
-
-
Arend, M.1
Westerman, B.2
Risch, N.3
-
40
-
-
7644238907
-
Solvent- and catalyst-free selective Mannich reaction on catechols and parα-substituted phenols: A convenient route to catecholand phenol-iminodiacetic acid ligands
-
(a) D'Hardemare, A. du M.; Jarjayes, O.; Mortini, F. Solvent- and catalyst-free selective Mannich reaction on catechols and parα-substituted phenols: A convenient route to catecholand phenol-iminodiacetic acid ligands. Synth. Commun. 2004, 34, 3975;
-
(2004)
Synth. Commun.
, vol.34
, pp. 3975
-
-
D'hardemare, A.1
Du, M.2
Jarjayes, O.3
Mortini, F.4
-
41
-
-
36348936614
-
Mannich type reactions of chlorophosphites, phosphoramides and aldehydes (ketones) under solvent-free and catalyst-free conditions- synthesis of N-phosphoramino a-aminophosphonates
-
(b) Zhang, J. F.; Cui, Z. W.; Wang, F.; Wang, Y.; Miao, Z. W.; Chen, R. Y. Mannich type reactions of chlorophosphites, phosphoramides and aldehydes (ketones) under solvent-free and catalyst-free conditions- synthesis of N-phosphoramino a-aminophosphonates. Green Chem. 2007, 9, 1341.
-
(2007)
Green Chem.
, vol.9
, pp. 1341
-
-
Zhang, J.F.1
Cui, Z.W.2
Wang, F.3
Wang, Y.4
Miao, Z.W.5
Chen, R.Y.6
|