nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A diversity-oriented synthesis of 3-(2-amino-1,6-dihydro-6-oxo-pyrimidin-5-yl)propanoic esters
|
Berzosa, Xavier |
|
2010 |
15 |
2 |
p. 595-601 |
artikel |
2 |
A diversity-oriented synthesis of pyrazolo[4,3-f]quinoline derivatives with potential bioactivities via microwave-assisted multi-component reactions
|
Shi, Feng |
|
2010 |
15 |
2 |
p. 497-505 |
artikel |
3 |
A mild and efficient method for the synthesis of a new class of furo[3,2-c]chromenes in aqueous media
|
Khalilzadeh, Mohammad A. |
|
2010 |
15 |
2 |
p. 445-450 |
artikel |
4 |
A multicomponent approach to the synthesis of 1,3-dicarbonylic compounds
|
Neo, Ana G. |
|
2010 |
15 |
2 |
p. 529-539 |
artikel |
5 |
A novel four-component reaction for the synthesis of disubstituted 1,3,4-oxadiazole derivatives
|
Ramazani, Ali |
|
2010 |
15 |
2 |
p. 521-527 |
artikel |
6 |
Carbonic anhydrase inhibition with natural products: novel chemotypes and inhibition mechanisms
|
Supuran, Claudiu T. |
|
2010 |
15 |
2 |
p. 305-316 |
artikel |
7 |
Chemical biology of Histone acetyltransferase natural compounds modulators
|
Piaz, Fabrizio Dal |
|
2010 |
15 |
2 |
p. 401-416 |
artikel |
8 |
CoMFA and CoMSIA of diverse pyrrolidine analogues as dipeptidyl peptidase IV inhibitors: active site requirements
|
Murugesan, Vanangamudi |
|
2010 |
15 |
2 |
p. 457-466 |
artikel |
9 |
Design, synthesis and activity evaluation of mannose-based DC-SIGN antagonists
|
Obermajer, Nataša |
|
2010 |
15 |
2 |
p. 347-360 |
artikel |
10 |
Design, synthesis and activity evaluation of mannose-based DC-SIGN antagonists
|
Obermajer, Nataša |
|
|
15 |
2 |
p. 347-360 |
artikel |
11 |
Diversity through semisynthesis: the chemistry and biological activity of semisynthetic epothilone derivatives
|
Altmann, Karl-Heinz |
|
2010 |
15 |
2 |
p. 383-399 |
artikel |
12 |
Domino Michael–O-alkylation: one-pot synthesis of dialkyl 4-oxo-2,3-dihydro-2,3-furandicarboxylates
|
Yavari, Issa |
|
2010 |
15 |
2 |
p. 451-456 |
artikel |
13 |
First computational chemistry multi-target model for anti-Alzheimer, anti-parasitic, anti-fungi, and anti-bacterial activity of GSK-3 inhibitors in vitro, in vivo, and in different cellular lines
|
García, Isela |
|
2010 |
15 |
2 |
p. 561-567 |
artikel |
14 |
HPLC-based activity profiling for GABAA receptor modulators from the traditional Chinese herbal drug Kushen (Sophora flavescens root)
|
Yang, Xinzhou |
|
2011 |
15 |
2 |
p. 361-372 |
artikel |
15 |
Integration-mediated prediction enrichment of quantitative model for Hsp90 inhibitors as anti-cancer agents: 3D-QSAR study
|
Roy, Kuldeep K. |
|
2010 |
15 |
2 |
p. 477-489 |
artikel |
16 |
Libraries of 2β-(N-substituted piperazino)-5α-androstane-3α, 17β-diols: chemical synthesis and cytotoxic effects on human leukemia HL-60 cells and on normal lymphocytes
|
Roy, Jenny |
|
2010 |
15 |
2 |
p. 317-339 |
artikel |
17 |
Molecular diversity and natural products
|
Appendino, Giovanni |
|
2011 |
15 |
2 |
p. 291-292 |
artikel |
18 |
Natural products as DNA methyltransferase inhibitors: a computer-aided discovery approach
|
Medina-Franco, Jose L. |
|
2010 |
15 |
2 |
p. 293-304 |
artikel |
19 |
Novel and efficient one-pot five- and six-component reactions for the stereoselective synthesis of highly functionalized enaminones and dithiocarbamates
|
Bararjanian, Morteza |
|
2010 |
15 |
2 |
p. 583-594 |
artikel |
20 |
Novel coumarin-based tyrosinase inhibitors discovered by OECD principles-validated QSAR approach from an enlarged, balanced database
|
Le-Thi-Thu, Huong |
|
2010 |
15 |
2 |
p. 507-520 |
artikel |
21 |
One-pot microwave-assisted protocol for the synthesis of substituted 2-amino-1H-imidazoles
|
Ermolat’ev, D. S. |
|
2010 |
15 |
2 |
p. 491-496 |
artikel |
22 |
Oral LD50 toxicity modeling and prediction of per- and polyfluorinated chemicals on rat and mouse
|
Bhhatarai, Barun |
|
2010 |
15 |
2 |
p. 467-476 |
artikel |
23 |
Prediction of mucin-type O-glycosylation sites by a two-staged strategy
|
Cai, YuDong |
|
2010 |
15 |
2 |
p. 427-433 |
artikel |
24 |
Prediction of mucin-type O-glycosylation sites by a two-staged strategy
|
Cai, YuDong |
|
|
15 |
2 |
p. 427-433 |
artikel |
25 |
Predictive models for nucleoside bisubstrate analogs as inhibitors of siderophore biosynthesis in Mycobacterium tuberculosis: pharmacophore mapping and chemometric QSAR study
|
Tawari, Nilesh R. |
|
2010 |
15 |
2 |
p. 435-444 |
artikel |
26 |
Quantitative structure–activity relationship study of antitubercular fluoroquinolones
|
Minovski, Nikola |
|
2010 |
15 |
2 |
p. 417-426 |
artikel |
27 |
Silica sulfuric acid as mild and efficient catalyst for the preparation of poly-hydroxyl aromatic compounds under mild and heterogeneous conditions
|
Khalafi-Nezhad, Ali |
|
2011 |
15 |
2 |
p. 373-381 |
artikel |
28 |
Synthesis of bis-peptides attached on poly[n]norbornene molecular scaffolds with well-defined relative positions and distances
|
Shang, Muhong |
|
2010 |
15 |
2 |
p. 541-560 |
artikel |
29 |
Traceless synthesis of diketopiperazine fused tetrahydro-β-carbolines on soluble polymer support
|
Chanda, Kaushik |
|
2010 |
15 |
2 |
p. 569-581 |
artikel |
30 |
Ultrasonic assisted Fischer glycosylation: generating diversity for glycochemistry
|
Shaikh, Nasrin |
|
2010 |
15 |
2 |
p. 341-345 |
artikel |