-
1
-
-
31544434530
-
Recent developments in isocyanide based multicomponent reactions in applied chemistry
-
DOI 10.1021/cr0505728
-
A Dömling 2006 Recent developments in isocyanide based multicomponent reactions in applied chemistry Chem Rev 106 17 89 10.1021/cr0505728 10.1021/cr0505728 16402771 (Pubitemid 43159621)
-
(2006)
Chemical Reviews
, vol.106
, Issue.1
, pp. 17-89
-
-
Domling, A.1
-
2
-
-
0037238724
-
"Multi-component reactions: Emerging chemistry in drug discovery" 'from Xylocain to Crixivan'
-
DOI 10.2174/0929867033368600
-
C Hulme V Gore 2003 Multi-component reactions: emerging chemistry in drug discovery 'from xylocain to crixivan' Curr Med Chem 10 51 80 10.2174/0929867033368600 10.2174/0929867033368600 1:CAS:528: DC%2BD3sXisVSrtA%3D%3D 12570721 (Pubitemid 36131649)
-
(2003)
Current Medicinal Chemistry
, vol.10
, Issue.1
, pp. 51-80
-
-
Hulme, C.1
Gore, V.2
-
3
-
-
0037391570
-
Recent developments in the isonitrile-based multicomponent synthesis of heterocycles
-
doi: 10.1002/ejoc.200390167
-
Zhu J (2003) Recent developments in the isonitrile-based multicomponent synthesis of heterocycles. Eur J Org Chem 1133-1144 doi: 10.1002/ejoc.200390167
-
(2003)
Eur J Org Chem
, vol.1133-1144
-
-
Zhu, J.1
-
4
-
-
34547403674
-
IBX-mediated oxidative Ugi-type multicomponent reactions: Application to the N and C1 functionalization of tetrahydroisoquinoline
-
DOI 10.1002/anie.200701603
-
T Ngouansavanh J Zhu 2007 IBX-mediated oxidative Ugi-type multicomponent reactions: application to the N and C1 functionalization of tetrahydroisoquinoline Angew Chem Int Ed 46 5775 5778 10.1002/anie.200701603 10.1002/anie.200701603 1:CAS:528:DC%2BD2sXosFGmsL8%3D (Pubitemid 47172210)
-
(2007)
Angewandte Chemie - International Edition
, vol.46
, Issue.30
, pp. 5775-5778
-
-
Ngouansavanh, T.1
Zhu, J.2
-
5
-
-
33748921576
-
Direct access to heterocyclic scaffolds by new multicomponent Ugi-Smiles couplings
-
DOI 10.1021/ol061605o
-
EK Laurent M Gizolme L Grimaud J Oble 2006 Direct access to heterocyclic scaffolds by new multicomponent Ugi-smiles couplings Org Lett 8 4019 4021 10.1021/ol061605o 10.1021/ol061605o (Pubitemid 44432842)
-
(2006)
Organic Letters
, vol.8
, Issue.18
, pp. 4019-4021
-
-
El Kaim, L.1
Gizolme, M.2
Grimaud, L.3
Oble, J.4
-
6
-
-
33750309194
-
Atom economy-a challenge for organic synthesis: Homogeneous catalysis Leads the Way
-
10.1002/anie.199502591 10.1002/anie.199502591 1:CAS:528: DyaK2MXjvFCisL0%3D
-
BM Trost 1995 Atom economy-a challenge for organic synthesis: homogeneous catalysis Leads the Way Angew Chem Int Ed Engl 34 259 281 10.1002/anie. 199502591 10.1002/anie.199502591 1:CAS:528:DyaK2MXjvFCisL0%3D
-
(1995)
Angew Chem Int Ed Engl
, vol.34
, pp. 259-281
-
-
Trost, B.M.1
-
7
-
-
0036424932
-
The application of multi-component reactions in drug discovery
-
1:CAS:528:DC%2BD38XoslKiur8%3D 12470248
-
L Weber 2002 The application of multi-component reactions in drug discovery Curr Med Chem 9 2085 2093 1:CAS:528:DC%2BD38XoslKiur8%3D 12470248
-
(2002)
Curr Med Chem
, vol.9
, pp. 2085-2093
-
-
Weber, L.1
-
8
-
-
34447101448
-
Design of sustainable chemical products - The example of ionic liquids
-
DOI 10.1021/cr050942s
-
J Ranke S Stolter R Strömann J Arning B Jastorff 2007 Design of sustainable chemical products-the example of ionic liquids Chem Rev 107 2183 2206 10.1021/cr050942s 10.1021/cr050942s 1:CAS:528:DC%2BD2sXmtlaks78%3D 17564479 (Pubitemid 47029092)
-
(2007)
Chemical Reviews
, vol.107
, Issue.6
, pp. 2183-2206
-
-
Ranke, J.1
Stolte, S.2
Stormann, R.3
Aming, J.4
Jastorff, B.5
-
9
-
-
35648978105
-
Effects of different head groups and functionalised side chains on the aquatic toxicity of ionic liquids
-
10.1039/b711119c 10.1039/b711119c 1:CAS:528:DC%2BD2sXht1Ghs73N
-
S Stolte M Matzke J Arning A Böschen WR Pitner U Welz-Biermann B Jastorff R Ranke 2007 Effects of different head groups and functionalised side chains on the aquatic toxicity of ionic liquids Green Chem 9 1170 1179 10.1039/b711119c 10.1039/b711119c 1:CAS:528:DC%2BD2sXht1Ghs73N
-
(2007)
Green Chem
, vol.9
, pp. 1170-1179
-
-
Stolte, S.1
Matzke, M.2
Arning, J.3
Böschen, A.4
Pitner, W.R.5
Welz-Biermann, U.6
Jastorff, B.7
Ranke, R.8
-
10
-
-
34347272296
-
Efficient catalyst reuse by simple dissolution in non-conventional media
-
DOI 10.1039/b607483a
-
Afonsa CAM, Branco LC, Candeias NR, Gois PMP, Lourenco NMT, Mateus NMM, Rosa JN (2007) Efficient catalyst reuse by simple dissolution in non-conventional media. Chem Commun 2669-2679 doi: 10.1039/b607483a (Pubitemid 47000778)
-
(2007)
Chemical Communications
, Issue.26
, pp. 2669-2679
-
-
Afonso, C.A.M.1
Branco, L.C.2
Candeias, N.R.3
Gois, P.M.P.4
Lourenco, N.M.T.5
Mateus, N.M.M.6
Rosa, J.N.7
-
11
-
-
34447098295
-
Catalysis in ionic liquids
-
DOI 10.1021/cr050948h
-
VI Parvulescu C Hardacre 2007 Catalysis in ionic liquids Chem Rev 107 2615 2665 10.1021/cr050948h 10.1021/cr050948h 1:CAS:528:DC%2BD2sXlsFOkt7c%3D 17518502 (Pubitemid 47029102)
-
(2007)
Chemical Reviews
, vol.107
, Issue.6
, pp. 2615-2665
-
-
Parvulescu, V.I.1
Hardacre, C.2
-
12
-
-
0020081045
-
Modulation of benzodiazepine receptor binding: Insight into pharmacological efficacy
-
10.1016/0014-2999(82)90246-1 10.1016/0014-2999(82)90246-1 1:CAS:528:DyaL38XhsFGnt7g%3D 6281035
-
FJ Ehlert P Ragan A Chen WR Roeske HI Yamamura 1982 Modulation of benzodiazepine receptor binding: insight into pharmacological efficacy Eur J Pharmacol 78 249 253 10.1016/0014-2999(82)90246-1 10.1016/0014-2999(82)90246-1 1:CAS:528:DyaL38XhsFGnt7g%3D 6281035
-
(1982)
Eur J Pharmacol
, vol.78
, pp. 249-253
-
-
Ehlert, F.J.1
Ragan, P.2
Chen, A.3
Roeske, W.R.4
Yamamura, H.I.5
-
13
-
-
0024516177
-
Synthesis and biological evaluation of certain C-4 substituted pyrazolo[3,4-b]pyridine nucleosides
-
DOI 10.1021/jm00125a004
-
YS Sanghvi SB Larson RC Willis RK Robins GR Revankar 1989 Synthesis and biological evaluation of certain C-4 substituted pyrazolo[3,4-b]pyridine nucleosides J Med Chem 32 945 951 10.1021/jm00125a004 10.1021/jm00125a004 1:CAS:528:DyaL1MXhvFegsrk%3D 2709381 (Pubitemid 19122140)
-
(1989)
Journal of Medicinal Chemistry
, vol.32
, Issue.5
, pp. 945-951
-
-
Sanghvi, Y.S.1
Larson, S.B.2
Willis, R.C.3
Robins, R.K.4
Revankar, G.R.5
-
14
-
-
77957031694
-
Chemistry of pyrazoles condensed to heteroaromatic five- and six-membered rings
-
10.1016/S0065-2725(08)60340-2 10.1016/S0065-2725(08)60340-2 1:CAS:528:DyaK3MXkt1Gqtg%3D%3D
-
MN Elnagdi M Rifaat H Elmoghayar KU Sadek 1990 Chemistry of pyrazoles condensed to heteroaromatic five- and six-membered rings Adv Heterocycl Chem 48 223 299 10.1016/S0065-2725(08)60340-2 10.1016/S0065-2725(08)60340-2 1:CAS:528:DyaK3MXkt1Gqtg%3D%3D
-
(1990)
Adv Heterocycl Chem
, vol.48
, pp. 223-299
-
-
Elnagdi, M.N.1
Rifaat, M.2
Elmoghayar, H.3
Sadek, K.U.4
-
15
-
-
0000956164
-
The chemistry of pyrazolopyridines
-
10.1016/S0065-2725(08)60117-8 10.1016/S0065-2725(08)60117-8 1:CAS:528:DyaL2MXkt1anuro%3D
-
CR Hardy 1984 The chemistry of pyrazolopyridines Adv Heterocycl Chem 36 343 409 10.1016/S0065-2725(08)60117-8 10.1016/S0065-2725(08)60117-8 1:CAS:528:DyaL2MXkt1anuro%3D
-
(1984)
Adv Heterocycl Chem
, vol.36
, pp. 343-409
-
-
Hardy, C.R.1
-
16
-
-
33751104210
-
Synthesis, in vitro evaluation, and SAR studies of a potential antichagasic 1H-pyrazolo[3,4-b]pyridine series
-
DOI 10.1016/j.bmc.2006.09.067, PII S0968089606008157
-
LRS Dias MB Santos S de Albuquerque HC Castro AMT de Souza ACC Freitas MAV Divaio LM Cabral CR Rodrigues 2007 Synthesis, in vitro evaluation, and SAR studies of a potential antichagasic 1H-pyrazolo[3,4-b]pyridine series Bioorg Med Chem 15 211 219 10.1016/j.bmc.2006.09.067 10.1016/j.bmc.2006.09.067 1:CAS:528:DC%2BD28Xht1CmtrbJ 17064907 (Pubitemid 44767993)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.1
, pp. 211-219
-
-
Dias, L.R.S.1
Santos, M.B.2
Albuquerque, S.D.3
Castro, H.C.4
De Souza, A.M.T.5
Freitas, A.C.C.6
DiVaio, M.A.V.7
Cabral, L.M.8
Rodrigues, C.R.9
-
17
-
-
12444280004
-
6-Aryl-pyrazolo[3,4-b]pyridines: Potent inhibitors of glycogen synthase kinase-3 (GSK-3)
-
DOI 10.1016/S0960-894X(03)00645-0
-
J Witherington V Bordas A Gaiba NS Garton A Naylor AD Rawlings BP Slingsby DG Smith AK Takle RW Ward 2003 6-Aryl-pyrazolo[3,4-b]pyridines: potent inhibitors of glycogen synthase kinase-3 (GSK-3) Bioorg Med Chem Lett 13 3055 3057 10.1016/S0960-894X(03)00645-0 10.1016/S0960-894X(03)00645-0 1:CAS:528:DC%2BD3sXms1Gmtro%3D 12941332 (Pubitemid 36993635)
-
(2003)
Bioorganic and Medicinal Chemistry Letters
, vol.13
, Issue.18
, pp. 3055-3057
-
-
Witherington, J.1
Bordas, V.2
Gaiba, A.3
Garton, N.S.4
Naylor, A.5
Rawlings, A.D.6
Slingsby, B.P.7
Smith, D.G.8
Takle, A.K.9
Ward, R.W.10
-
18
-
-
34347387725
-
Synthesis and evaluation of pyrazolo[3,4-b]pyridine CDK1 inhibitors as anti-tumor agents
-
DOI 10.1016/j.bmcl.2007.05.029, PII S0960894X07005823
-
RH Lin PJ Connolly YH Lu G Chiu SJ Li Y Yu SL Huang X Li SL Emanuel SA Middleton RH Gruninger M Adams AR Fuentes-Pesquera LM Greenberger 2007 Synthesis and evaluation of pyrazolo[3,4-b]pyridine CDK1 inhibitors as anti-tumor agents Bioorg Med Chem Lett 17 4297 4302 10.1016/j.bmcl.2007.05.029 10.1016/j.bmcl.2007.05.029 1:CAS:528:DC%2BD2sXnsVKnu7w%3D 17532631 (Pubitemid 47021391)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.15
, pp. 4297-4302
-
-
Lin, R.1
Connolly, P.J.2
Lu, Y.3
Chiu, G.4
Li, S.5
Yu, Y.6
Huang, S.7
Li, X.8
Emanuel, S.L.9
Middleton, S.A.10
Gruninger, R.H.11
Adams, M.12
Fuentes-Pesquera, A.R.13
Greenberger, L.M.14
-
19
-
-
26844510933
-
Design, synthesis and biological activity of acyl substituted 3-amino-5-methyl-1,4,5,7-tetrahydropyrazolo[3,4-b]pyridin-6-ones as potential hypnotic drugs
-
DOI 10.1016/j.ejmech.2005.06.008, PII S0223523405001820
-
JL Falcó M Lloveras I Buira J Teixidó JI Borrell E Méndez J Terencio A Palomer A Guglietta 2005 Design, synthesis and biological activity of acyl substituted 3-amino-5-methyl-1,4,5,7- tetrahydropyrazolo[3,4-b]pyridin-6-ones as potential hypnotic drugs Eur J Med Chem 40 1179 1187 10.1016/j.ejmech.2005.06.008 10.1016/j.ejmech.2005.06.008 16095764 (Pubitemid 41446291)
-
(2005)
European Journal of Medicinal Chemistry
, vol.40
, Issue.11
, pp. 1179-1187
-
-
Falco, J.L.1
Lloveras, M.2
Buira, I.3
Teixido, J.4
Borrell, J.I.5
Mendez, E.6
Terencio, J.7
Palomer, A.8
Guglietta, A.9
-
20
-
-
33745123026
-
1-[3-Aminobenzisoxazol-5′-yl]-3-trifluoromethyl-6-[2′-(3-(R) -hydroxy-N-pyrrolidinyl)methyl-[1,1′]-biphen-4-yl]-1,4,5, 6-tetrahydropyrazolo-[3,4-c]-pyridin-7-one (BMS-740808) a highly potent, selective, efficacious, and orally bioavailable inhibitor of blood coagulation factor Xa
-
DOI 10.1016/j.bmcl.2006.02.069, PII S0960894X06002393
-
DJP Pinto MJ Orwat ML Quan Q Han RA Galemmo Jr E Amparo B Wells C Ellis MY He RS Alexander KA Rossi A Smallwood PC Wong JM Luettgen AR Rendina RM Knabb L Mersinger C Kettner S Bai K He RR Wexler PYS Lam 2006 1-[3-Aminobenzisoxazol- 5-yl]-3-trifluoromethyl-6-[2-(3-(R)-hydroxy-N-pyrrolidinyl)methyl-[1,1] -biphen-4-yl]-1,4,5,6-tetrahydropyrazolo-[3,4-c]-pyridin-7-one (BMS-740808) a highly potent, selective, efficacious, and orally bioavailable inhibitor of blood coagulation factor Xa Bioorg Med Chem Lett 16 4141 4147 10.1016/j.bmcl.2006.02.069 10.1016/j.bmcl.2006.02.069 1:CAS:528: DC%2BD28Xmt1Gguro%3D 16730984 (Pubitemid 43903191)
-
(2006)
Bioorganic and Medicinal Chemistry Letters
, vol.16
, Issue.15
, pp. 4141-4147
-
-
Pinto, D.J.P.1
Orwat, M.J.2
Quan, M.L.3
Han, Q.4
Galemmo Jr., R.A.5
Amparo, E.6
Wells, B.7
Ellis, C.8
He, M.Y.9
Alexander, R.S.10
Rossi, K.A.11
Smallwood, A.12
Wong, P.C.13
Luettgen, J.M.14
Rendina, A.R.15
Knabb, R.M.16
Mersinger, L.17
Kettner, C.18
Bai, S.19
He, K.20
Wexler, R.R.21
Lam, P.Y.S.22
more..
-
22
-
-
0020645555
-
New developments in calcium ion channel antagonists
-
10.1021/jm00360a001 10.1021/jm00360a001
-
RA Janos DJ Triggle 1983 New developments in calcium ion channel antagonists J Med Chem 26 775 785 10.1021/jm00360a001 10.1021/jm00360a001
-
(1983)
J Med Chem
, vol.26
, pp. 775-785
-
-
Janos, R.A.1
Triggle, D.J.2
-
23
-
-
34249111631
-
Facile synthesis of substituted 1H-pyrazolo[3,4-b]pyridines
-
10.1016/j.mencom.2007.05.022 1:CAS:528:DC%2BD2sXhtVelsr3O
-
GP Sagitullina LA Lisitskaya MA Vorontsova RS Sagitullin 2007 Facile synthesis of substituted 1H-pyrazolo[3,4-b]pyridines Mendeleev Commun 17 192 193 10.1016/j.mencom.2007.05.022 1:CAS:528:DC%2BD2sXhtVelsr3O
-
(2007)
Mendeleev Commun
, vol.17
, pp. 192-193
-
-
Sagitullina, G.P.1
Lisitskaya, L.A.2
Vorontsova, M.A.3
Sagitullin, R.S.4
-
24
-
-
0032787121
-
Synthesis of 5-cyanopyrazolo[3,4-b]pyridines in the reaction of 5-amino-3-methyl-1-phenylpyrazole with arylidene derivatives of malonodinitrile and ethyl cyanoacetate
-
10.1002/jhet.5570360533 10.1002/jhet.5570360533 1:CAS:528: DyaK1MXnvFOruro%3D
-
J Quiroga M Alvarado B Insuasty R Moreno E Ravina I Estevez RH de Almedia 1999 Synthesis of 5-cyanopyrazolo[3,4-b]pyridines in the reaction of 5-amino-3-methyl-1-phenylpyrazole with arylidene derivatives of malonodinitrile and ethyl cyanoacetate J Heterocycl Chem 36 1311 1316 10.1002/jhet.5570360533 10.1002/jhet.5570360533 1:CAS:528:DyaK1MXnvFOruro%3D
-
(1999)
J Heterocycl Chem
, vol.36
, pp. 1311-1316
-
-
Quiroga, J.1
Alvarado, M.2
Insuasty, B.3
Moreno, R.4
Ravina, E.5
Estevez, I.6
De Almedia, R.H.7
-
25
-
-
0031833851
-
Reaction of 5-amino-1-aryl-3-methylpyrazoles with benzylidene derivatives of Meldrum's acid: Synthesis and characterization of pyrazolo[3,4-b]pyridinones
-
10.1002/jhet.5570350225 10.1002/jhet.5570350225 1:CAS:528: DyaK1cXjsVSrsrg%3D
-
J Quiroga A Hormaza B Insuasty M Marquez 1998 Reaction of 5-amino-1-aryl-3-methylpyrazoles with benzylidene derivatives of Meldrum's acid: synthesis and characterization of pyrazolo[3,4-b]pyridinones J Heterocycl Chem 35 409 412 10.1002/jhet.5570350225 10.1002/jhet.5570350225 1:CAS:528: DyaK1cXjsVSrsrg%3D
-
(1998)
J Heterocycl Chem
, vol.35
, pp. 409-412
-
-
Quiroga, J.1
Hormaza, A.2
Insuasty, B.3
Marquez, M.4
-
26
-
-
0035086144
-
Synthesis and structural analysis of 5-cyanodihydropyrazolo[3,4-b] pyridines
-
10.1002/jhet.5570380108 10.1002/jhet.5570380108 1:CAS:528: DC%2BD3MXit1ehsr8%3D
-
J Quiroga S Kruz B Insuasty R Abonia M Nogueras A Sanchez J Cobo JN Low 2001 Synthesis and structural analysis of 5-cyanodihydropyrazolo[3,4-b]pyridines J Heterocycl Chem 38 53 60 10.1002/jhet.5570380108 10.1002/jhet.5570380108 1:CAS:528:DC%2BD3MXit1ehsr8%3D
-
(2001)
J Heterocycl Chem
, vol.38
, pp. 53-60
-
-
Quiroga, J.1
Kruz, S.2
Insuasty, B.3
Abonia, R.4
Nogueras, M.5
Sanchez, A.6
Cobo, J.7
Low, J.N.8
-
27
-
-
26044449378
-
Synthesis of 6-amino-4-aryl-5-cyano-3-methyl-1-phenylpyridino-[2,3-c] pyrazole under microwave irradiation
-
1:CAS:528:DC%2BD2MXpsVehtbs%3D (in Chinese)
-
S Zhu S Tu T Li X Zhang S Ji Y Zhang 2005 Synthesis of 6-amino-4-aryl-5-cyano-3-methyl-1-phenylpyridino-[2,3-c]pyrazole under microwave irradiation Chin J Org Chem 25 987 990 1:CAS:528:DC%2BD2MXpsVehtbs%3D (in Chinese)
-
(2005)
Chin J Org Chem
, vol.25
, pp. 987-990
-
-
Zhu, S.1
Tu, S.2
Li, T.3
Zhang, X.4
Ji, S.5
Zhang, Y.6
-
28
-
-
32044452211
-
One-step synthesis of 4-aryl-3-methyl-6-oxo-1-phenyl-4,5,6,7- tetrahydropyrido[2,3-c]pyrazole under microwave irradiation
-
S Tu S Zhu Z Shao X Zou S Ji Y Zhang 2005 One-step synthesis of 4-aryl-3-methyl-6-oxo-1-phenyl-4,5,6,7-tetrahydropyrido[2,3-c]pyrazole under microwave irradiation Chin J Org Chem 25 1552 1555 1:CAS:528:DC%2BD2MXhtlWlurzK (in Chinese) (Pubitemid 43198914)
-
(2005)
Chinese Journal of Organic Chemistry
, vol.25
, Issue.12
, pp. 1552-1555
-
-
Tu, S.-J.1
Zhu, S.-L.2
Shao, Z.3
Zou, X.4
Ji, S.-J.5
Zhang, Y.6
-
29
-
-
36749079869
-
Design and synthesis of new and significative bifunctional compounds containing two pyrazolo[3,4-b]pyridine nucleis through multicomponent reaction under microwave irradiation
-
10.1002/jhet.5570440409 10.1002/jhet.5570440409 1:CAS:528: DC%2BD2sXns1yjsrk%3D
-
S Tu Q Wang Y Zhang J Xu J Zhang X Zhu F Shi 2007 Design and synthesis of new and significative bifunctional compounds containing two pyrazolo[3,4-b]pyridine nucleis through multicomponent reaction under microwave irradiation J Heterocycl Chem 44 811 814 10.1002/jhet.5570440409 10.1002/jhet.5570440409 1:CAS:528:DC%2BD2sXns1yjsrk%3D
-
(2007)
J Heterocycl Chem
, vol.44
, pp. 811-814
-
-
Tu, S.1
Wang, Q.2
Zhang, Y.3
Xu, J.4
Zhang, J.5
Zhu, X.6
Shi, F.7
-
30
-
-
0035806284
-
Microwave assisted solvent-free synthesis of pyrazolo[3,4-b]quinolines and pyrazolo[3,4-c]pyrazoles using p-TsOH
-
DOI 10.1016/S0040-4039(01)00505-6, PII S0040403901005056
-
S Paul M Gupta R Gupta A Loupy 2001 Microwave assisted solvent-free synthesis of pyrazolo[3,4-b]quinolines and pyrazolo[3,4-c]pyrazoles using p-TsOH Tetrahedron Lett 42 3827 3829 10.1016/S0040-4039(01)00505-6 10.1016/S0040-4039(01)00505-6 1:CAS:528:DC%2BD3MXjslanurg%3D (Pubitemid 32493763)
-
(2001)
Tetrahedron Letters
, vol.42
, Issue.23
, pp. 3827-3829
-
-
Paul, S.1
Gupta, M.2
Gupta, R.3
Loupy, A.4
-
31
-
-
0031878132
-
Synthesis of 4-aryl-4,7,8,9-tetrahydro-6H-pyrazolo[3,4-b]quinolin-5-ones
-
10.1002/jhet.5570350313 10.1002/jhet.5570350313 1:CAS:528: DyaK1cXltFKrtb0%3D
-
J Quiroga B Insuasty A Hormaza C Saitz C Jullian 1998 Synthesis of 4-aryl-4,7,8,9-tetrahydro-6H-pyrazolo[3,4-b]quinolin-5-ones J Heterocycl Chem 35 575 578 10.1002/jhet.5570350313 10.1002/jhet.5570350313 1:CAS:528: DyaK1cXltFKrtb0%3D
-
(1998)
J Heterocycl Chem
, vol.35
, pp. 575-578
-
-
Quiroga, J.1
Insuasty, B.2
Hormaza, A.3
Saitz, C.4
Jullian, C.5
-
32
-
-
32044461094
-
Facile three component one-pot synthesis of 5-aryl-1,5,6,7,8,9-hexahydro- 2H-pyrazolo[5,4-b]quinolin-6-one derivatives under microwave irradiation
-
1:CAS:528:DC%2BD2MXhtlWlurrP (in Chinese)
-
GP Hua JN Xu SJ Tu Q Wang JP Zhang XT Zhu TJ Li SL Zhu XJ Zhang 2005 Facile three component one-pot synthesis of 5-aryl-1,5,6,7,8,9-hexahydro-2H- pyrazolo[5,4-b]quinolin-6-one derivatives under microwave irradiation Chin J Org Chem 25 1610 1614 1:CAS:528:DC%2BD2MXhtlWlurrP (in Chinese)
-
(2005)
Chin J Org Chem
, vol.25
, pp. 1610-1614
-
-
Hua, G.P.1
Xu, J.N.2
Tu, S.J.3
Wang, Q.4
Zhang, J.P.5
Zhu, X.T.6
Li, T.J.7
Zhu, S.L.8
Zhang, X.J.9
-
33
-
-
10644266961
-
Ionic liquid promoted Knoevenagel and Michael reactions
-
10.1071/CH04060 10.1071/CH04060 1:CAS:528:DC%2BD2cXpvVGksbs%3D
-
X Fan X Hu X Zhang J Wang 2004 Ionic liquid promoted Knoevenagel and Michael reactions Aust J Chem 57 1067 1071 10.1071/CH04060 10.1071/CH04060 1:CAS:528:DC%2BD2cXpvVGksbs%3D
-
(2004)
Aust J Chem
, vol.57
, pp. 1067-1071
-
-
Fan, X.1
Hu, X.2
Zhang, X.3
Wang, J.4
-
34
-
-
16444368466
-
2O-promoted green preparation of xanthenedione derivatives in ionic liquids
-
DOI 10.1139/v04-155
-
2O Promoted green preparation of xanthenedione derivatives in ionic liquids Can J Chem 83 16 20 10.1139/v04-155 10.1139/v04-155 1:CAS:528:DC%2BD2MXjtlSht7Y%3D (Pubitemid 40477616)
-
(2005)
Canadian Journal of Chemistry
, vol.83
, Issue.1
, pp. 16-20
-
-
Fan, X.1
Hu, X.2
Zhang, X.3
Wang, J.4
-
35
-
-
33747037475
-
4])
-
DOI 10.1139/V06-070
-
X Fan Y Li X Zhang G Qu J Wang 2006 A novel and green version of the Passerini reaction in an ionic liquid ([bmim][BF4]) Can J Chem 84 794 799 10.1139/V06-070 10.1139/V06-070 1:CAS:528:DC%2BD28XkvVyks7c%3D (Pubitemid 44213463)
-
(2006)
Canadian Journal of Chemistry
, vol.84
, Issue.5
, pp. 794-799
-
-
Fan, X.1
Li, Y.2
Zhang, X.3
Qu, G.4
Wang, J.5
-
37
-
-
33745833395
-
Toward orthopoxvirus countermeasures: A novel heteromorphic nucleoside of unusual structure
-
DOI 10.1021/jm060404n
-
X Fan X Zhang L Zhou KA Keith MN Prichard ER Kern PF Torrence 2006 Toward orthopoxvirus countermeasures: a novel heteromorphic nucleoside of unusual structure J Med Chem 49 4052 4054 10.1021/jm060404n 10.1021/jm060404n 1:CAS:528:DC%2BD28XmtVSisrk%3D 16821766 (Pubitemid 44036651)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.14
, pp. 4052-4054
-
-
Fan, X.1
Zhang, X.2
Zhou, L.3
Keith, K.A.4
Prichard, M.N.5
Kern, E.R.6
Torrence, P.F.7
-
38
-
-
33744793223
-
5-(Dimethoxymethyl)-2′-deoxyuridine: A novel gem diether nucleoside with anti-orthopoxvirus activity
-
DOI 10.1021/jm0601710
-
X Fan X Zhang L Zhou KA Keith MN Prichard ER Kern PF Torrence 2006 5-(dimethoxymethyl)-2'-deoxyuridine: a novel gem diether nucleoside with anti-orthopoxvirus activity J Med Chem 49 3377 3382 10.1021/jm0601710 10.1021/jm0601710 1:CAS:528:DC%2BD28XjvFKqtrk%3D 16722657 (Pubitemid 43830536)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.11
, pp. 3377-3382
-
-
Fan, X.1
Zhang, X.2
Zhou, L.3
Keith, K.A.4
Kern, E.R.5
Torrence, P.F.6
-
39
-
-
33747147736
-
Assembling a smallpox biodefense by interrogating 5-substituted pyrimidine nucleoside chemical space
-
DOI 10.1016/j.antiviral.2006.04.015, PII S0166354206001240
-
X Fan X Zhang L Zhou KA Keith MN Prichard ER Kern PF Torrence 2006 Assembling a smallpox biodefense by interrogating 5-substituted pyrimidine nucleoside chemical space Antiviral Res 71 201 205 10.1016/j.antiviral.2006.04. 015 10.1016/j.antiviral.2006.04.015 1:CAS:528:DC%2BD28XotlGkt7c%3D 16759713 (Pubitemid 44223764)
-
(2006)
Antiviral Research
, vol.71
, Issue.2-3 SPEC. ISS.
, pp. 201-205
-
-
Fan, X.1
Zhang, X.2
Zhou, L.3
Keith, K.A.4
Kern, E.R.5
Torrence, P.F.6
-
40
-
-
33747095922
-
A pyrimidine-pyrazolone nucleoside chimera with potent in vitro anti-orthopoxvirus activity
-
DOI 10.1016/j.bmcl.2006.03.043, PII S0960894X06003362
-
X Fan X Zhang L Zhou KA Keith MN Prichard ER Kern PF Torrence 2006 A pyrimidine-pyrazolone nucleoside chimera with potent in vitro anti-orthopoxvirus activity Bioorg Med Chem Lett 16 3224 3228 10.1016/j.bmcl.2006.03.043 10.1016/j.bmcl.2006.03.043 1:CAS:528:DC%2BD28XksFeqsr0%3D 16603351 (Pubitemid 44287967)
-
(2006)
Bioorganic and Medicinal Chemistry Letters
, vol.16
, Issue.12
, pp. 3224-3228
-
-
Fan, X.1
Zhang, X.2
Zhou, L.3
Keith, K.A.4
Kern, E.R.5
Torrence, P.F.6
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