nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A convenient four-component one-pot synthesis of 2-amino-1,3,4-thiadiazoles in water
|
Liu, Peng |
|
2014 |
18 |
4 |
p. 737-743 |
artikel |
2 |
A green four-component synthesis of zwitterionic alkyl/benzyl pyrazolyl barbiturates and their photophysical studies
|
Bihani, Manisha |
|
2014 |
18 |
4 |
p. 745-757 |
artikel |
3 |
An efficient strategy to syntheses of isoflavones
|
Liu, Longzhu |
|
2014 |
18 |
4 |
p. 777-785 |
artikel |
4 |
An efficient three-component synthesis of highly functionalized tetrahydroacenaphtho[1,2-$$b$$b]indolone derivatives catalyzed by L-proline
|
Zhang, Juan-Juan |
|
2014 |
18 |
4 |
p. 727-736 |
artikel |
5 |
An in silico protocol for identifying mTOR inhibitors from natural products
|
Chen, Lei |
|
2014 |
18 |
4 |
p. 841-852 |
artikel |
6 |
A simple and efficient synthesis of fused morpholine pyrrolidines/piperdines with potential insecticidal activities
|
Wang, Jiayi |
|
2014 |
18 |
4 |
p. 887-893 |
artikel |
7 |
A tandem synthesis of 5-sulfonylimino-2-imidazolones from sulfonoketenimides and dialkyl azodicarboxylates
|
Yavari, Issa |
|
2014 |
18 |
4 |
p. 721-725 |
artikel |
8 |
Catalytic enantioselective diversity-oriented synthesis of a small library of polyhydroxylated pyrans inspired from thiomarinol antibiotics
|
Al-Zoubi, Raed M. |
|
2014 |
18 |
4 |
p. 701-719 |
artikel |
9 |
Design, synthesis, and biological activities of novel azole-bonded $$\upbeta $$β-hydroxypropyl oxime O-ethers
|
Behrouz, Somayeh |
|
2014 |
18 |
4 |
p. 797-808 |
artikel |
10 |
Diaminoglyoxime as a versatile reagent in the synthesis of bis(1,2,4-oxadiazoles), 1,2,4-oxadiazolyl-quinazolines and 1,2,4-oxadiazolyl-benzothiazinones
|
Khanmiri, Rahim Hosseinzadeh |
|
2014 |
18 |
4 |
p. 769-776 |
artikel |
11 |
Efficient synthesis of functionalized spiro[indoline-3,4$$^{\prime }$$′-pyrrolo[3,4-b]pyridines] via one-pot three-component reaction
|
Wang, Chao |
|
2014 |
18 |
4 |
p. 809-820 |
artikel |
12 |
Identification of new novel scaffold for Aurora A inhibition by pharmacophore modeling and virtual screening
|
Chavan, Sayalee R. |
|
2014 |
18 |
4 |
p. 853-863 |
artikel |
13 |
LBVS: an online platform for ligand-based virtual screening using publicly accessible databases
|
Zheng, Minghao |
|
2014 |
18 |
4 |
p. 829-840 |
artikel |
14 |
Microwave-assisted one-pot multi-component reaction: synthesis of novel and highly functionalized 3-(pyranyl)- and 3-(dihydropyridinyl)indole derivatives
|
Borah, Pallabi |
|
2014 |
18 |
4 |
p. 759-767 |
artikel |
15 |
$$N$$N-Polybenzylated alicyclic 1,2-diamines: cytotoxicity and G1 phase arrest in cancer cell line
|
Caldarelli, Antonio |
|
2014 |
18 |
4 |
p. 879-886 |
artikel |
16 |
One-pot diastreoselective synthesis of highly functionalized cyclohexenones: 2-oxo-N,4,6-triarylcyclohex-3-enecarboxamides
|
Mousavi, Mir Rasul |
|
2014 |
18 |
4 |
p. 821-828 |
artikel |
17 |
Predicting drug metabolism by CYP1A1, CYP1A2, and CYP1B1: insights from MetaSite, molecular docking and quantum chemical calculations
|
Pragyan, Preeti |
|
2014 |
18 |
4 |
p. 865-878 |
artikel |
18 |
Pregnane X Receptor and P-glycoprotein: a connexion for Alzheimer’s disease management
|
Jain, Sumit |
|
2014 |
18 |
4 |
p. 895-909 |
artikel |
19 |
Synthesis of benzimidazole[2.1-b][1,3]oxazine spirooxindoles via three-component reaction of N-benzylbenzimidazole, acetylenedicarboxylates, and N-alkylisatins
|
Zhang, Li-Juan |
|
2014 |
18 |
4 |
p. 787-796 |
artikel |