| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An efficient multistep ligand-based virtual screening approach for GPR40 agonists
|
Yao, Sihui
|
|
2013
|
18 |
1 |
p. 183-193
|
artikel
|
| 2 |
Design, synthesis, and anti-tobacco mosaic virus (TMV) activity of glycoconjugates of phenanthroindolizidines alkaloids
|
Wu, Meng
|
|
2013
|
18 |
1 |
p. 25-37
|
artikel
|
| 3 |
Design, synthesis, and anti-tobacco mosaic virus (TMV) activity of glycoconjugates of phenanthroindolizidines alkaloids
|
Wu, Meng
|
|
|
18 |
1 |
p. 25-37
|
artikel
|
| 4 |
Discovering Echinococcus granulosus thioredoxin glutathione reductase inhibitors through site-specific dynamic combinatorial chemistry
|
Saiz, Cecilia
|
|
2013
|
18 |
1 |
p. 1-12
|
artikel
|
| 5 |
Docking and quantitative structure–activity relationship of oxadiazole derivates as inhibitors of GSK3$$\upbeta $$β
|
Quesada-Romero, Luisa
|
|
2013
|
18 |
1 |
p. 149-159
|
artikel
|
| 6 |
Efficient one-pot synthesis of novel and diverse tetrahydroquinolines bearing pyranopyrazoles using organocatalyzed domino Knoevenagel/hetero Diels–Alder reactions
|
Pandit, Rameshwar Prasad
|
|
2013
|
18 |
1 |
p. 39-50
|
artikel
|
| 7 |
Efficient synthesis of 4-oxo-4,5-dihydrothieno[3,2-$$c$$c]quinoline-2-carboxylic acid derivatives from aniline
|
Chatterjee, Arindam
|
|
2013
|
18 |
1 |
p. 51-59
|
artikel
|
| 8 |
Expanding the substrate scope of ugi five-center, four-component reaction U-5C-4CR): ketones as coupling partners for secondary amino acids
|
Dawidowski, Maciej
|
|
2013
|
18 |
1 |
p. 61-77
|
artikel
|
| 9 |
Ionic liquid-supported synthesis of piperazine derivatives as potential insecticides
|
Shen, Yan
|
|
2013
|
18 |
1 |
p. 195-202
|
artikel
|
| 10 |
Iridium-catalyzed asymmetric ring-opening reactions of azabenzonorbornadiene with carboxylic acid nucleophiles
|
Long, Yuhua
|
|
2013
|
18 |
1 |
p. 101-110
|
artikel
|
| 11 |
New insights in the activation of human cholesterol esterase to design potent anti-cholesterol drugs
|
John, Shalini
|
|
2013
|
18 |
1 |
p. 119-131
|
artikel
|
| 12 |
Prediction of antiprion activity of therapeutic agents with structure–activity models
|
Venko, Katja
|
|
2013
|
18 |
1 |
p. 133-148
|
artikel
|
| 13 |
Pyrid-2-yl and 2-CyanoPhenyl fused heterocyclic compounds as human P2X$$_{3}$$3 inhibitors: a combined approach based on homology modelling, docking and QSAR analysis
|
Janardhan, Sridhara
|
|
2013
|
18 |
1 |
p. 161-181
|
artikel
|
| 14 |
Recent progress on fluorous synthesis of biologically interesting compounds
|
Jiang, Zhong-Xing
|
|
2014
|
18 |
1 |
p. 203-218
|
artikel
|
| 15 |
Selective MAO-B inhibitors: a lesson from natural products
|
Carradori, Simone
|
|
2013
|
18 |
1 |
p. 219-243
|
artikel
|
| 16 |
Synthesis and anti-cancer activity of a glycosyl library of $$\varvec{N}$$N-acetylglucosamine-bearing oleanolic acid
|
Zeng, Yi-Bing
|
|
2013
|
18 |
1 |
p. 13-23
|
artikel
|
| 17 |
Synthesis of 6a,6b,13,13a-tetrahydro-6H-5-oxa-12a-azadibenzo[a,g]fluorene derivatives via cycloaddition reactions of isoquinolinium salts with 3-nitrochromenes
|
Fang, Jun
|
|
2013
|
18 |
1 |
p. 91-99
|
artikel
|
| 18 |
Synthesis of new 1,5-diaryl-3-(arylamino)-1H-pyrrol-2(5H)-ones under catalyst-free and solvent-free conditions
|
Niknam, Khodabakhsh
|
|
2013
|
18 |
1 |
p. 111-117
|
artikel
|
| 19 |
Synthesis of tetrahydropyrimidin-2-ones via $$\hbox {FeCl}_{3}$$FeCl3 catalyzed one-pot domino reaction of amines, methyl propiolate, aromatic aldehydes, and urea
|
Zhang, Li-Li
|
|
2013
|
18 |
1 |
p. 79-89
|
artikel
|
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