| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A classification study of human β3-adrenergic receptor agonists using BCUT descriptors
|
Hao, Ming
|
|
2011
|
15 |
4 |
p. 877-887
|
artikel
|
| 2 |
A facile and one pot synthesis of 1,4-disubstituted-1H-1,2,3-triazoles from terminal alkynes and phenacyl azides prepared from styrenes by CAN oxidant and sodium azide
|
Keshavarz, Mosadegh
|
|
2011
|
15 |
4 |
p. 957-962
|
artikel
|
| 3 |
An integrated drug-likeness study for bicyclic privileged structures: from physicochemical properties to in vitro ADME properties
|
Han, Chunyan
|
|
2011
|
15 |
4 |
p. 857-876
|
artikel
|
| 4 |
An unexpected C–C cleavage reaction: new and mild access to o-OH and o-NH-Tos benzoic acids or benzoamides
|
Zheng, Purong
|
|
2011
|
15 |
4 |
p. 971-977
|
artikel
|
| 5 |
Efficient synthesis and free-radical scavenging capacity of new 2,4-substituted tetrahydroquinolines prepared via BiCl3-catalyzed three-component Povarov reaction, using N-vinylamides
|
Kouznetsov, Vladimir V.
|
|
2011
|
15 |
4 |
p. 1007-1016
|
artikel
|
| 6 |
Insights into the binding modes of human β3-adrenergic receptor agonists with ligand-based and receptor-based methods
|
Jin, Fangfang
|
|
2011
|
15 |
4 |
p. 817-831
|
artikel
|
| 7 |
Lithium perchlorate-nitromethane-promoted alkylation of anilines with arylmethanols
|
Zhou, Jun
|
|
2011
|
15 |
4 |
p. 849-855
|
artikel
|
| 8 |
Molecular dynamics directed CoMFA studies on carbocyclic neuraminidase inhibitors
|
Chavan, Swapnil
|
|
2011
|
15 |
4 |
p. 979-987
|
artikel
|
| 9 |
Multicomponent reactions of ammonium thiocyanate, acyl chlorides, alkyl bromides, and enaminones: A facile one-pot synthesis of thiophenes
|
Hossaini, Zinatossadat
|
|
2011
|
15 |
4 |
p. 911-916
|
artikel
|
| 10 |
One-pot synthesis of 1,2,3-triazole linked dihydropyrimidinones via Huisgen 1,3-dipolar/Biginelli cycloaddition
|
Salehi, Peyman
|
|
2011
|
15 |
4 |
p. 833-837
|
artikel
|
| 11 |
Parallel synthesis of novel antitumor agents: 1,2,3-triazoles bearing biologically active sulfonamide moiety and their 3D-QSAR
|
Ou, Lili
|
|
2011
|
15 |
4 |
p. 927-946
|
artikel
|
| 12 |
Parallel synthesis of novel antitumor agents: 1,2,3-triazoles bearing biologically active sulfonamide moiety and their 3D-QSAR
|
Ou, Lili
|
|
|
15 |
4 |
p. 927-946
|
artikel
|
| 13 |
Potent antimicrobial small molecules screened as inhibitors of tyrosine recombinases and Holliday junction-resolving enzymes
|
Rideout, Marc C.
|
|
2011
|
15 |
4 |
p. 989-1005
|
artikel
|
| 14 |
Potent antimicrobial small molecules screened as inhibitors of tyrosine recombinases and Holliday junction-resolving enzymes
|
Rideout, Marc C.
|
|
|
15 |
4 |
p. 989-1005
|
artikel
|
| 15 |
QSAR model toward the rational design of new agrochemical fungicides with a defined resistance risk using substructural descriptors
|
Speck-Planche, Alejandro
|
|
2011
|
15 |
4 |
p. 901-909
|
artikel
|
| 16 |
Synthesis of 1,5-benzothiazepine derivatives bearing 2-phenoxy-quinoline moiety via 1,3-diplolar cycloaddition reaction
|
Dong, Zhi-Qiang
|
|
2011
|
15 |
4 |
p. 963-970
|
artikel
|
| 17 |
Synthesis of highly substituted 2,3-dihydropyrimido[4,5-d]pyrimidin-4(1H)-ones from 4,6-dichloro-5-formylpyrimidine, amines and aldehydes
|
Xiang, Jinbao
|
|
2011
|
15 |
4 |
p. 839-847
|
artikel
|
| 18 |
Synthesis of novel 6-triazologlycolipids via click chemistry and their preliminary cytotoxicity assessments
|
Zhang, Hai-Lin
|
|
2011
|
15 |
4 |
p. 889-900
|
artikel
|
| 19 |
Targeting tuberculosis through a small focused library of 1,2,3-triazoles
|
Labadie, Guillermo R.
|
|
2011
|
15 |
4 |
p. 1017-1024
|
artikel
|
| 20 |
Theoretical study of GSK−3α: neural networks QSAR studies for the design of new inhibitors using 2D descriptors
|
García, Isela
|
|
2011
|
15 |
4 |
p. 947-955
|
artikel
|
| 21 |
Topological virtual screening: a way to find new compounds active in ulcerative colitis by inhibiting NF-κB
|
Gálvez-Llompart, María
|
|
2011
|
15 |
4 |
p. 917-926
|
artikel
|
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