| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A facile three- and four-component procedure toward the synthesis of functionalized pyrano- and benzo[f]quinoxaline derivatives
|
Ghadari, Rahim
|
|
2012
|
16 |
3 |
p. 453-461
|
article
|
| 2 |
An efficient three-component, one-pot synthesis of 2-alkylthio-4-amino-5-cyano-6-aryl(alkyl)pyrimidines in water
|
Li, Qiao-Yan
|
|
2012
|
16 |
3 |
p. 431-439
|
article
|
| 3 |
An efficient three-component, one-pot synthesis of 2-alkylthio-4-amino-5-cyano-6-aryl(alkyl)pyrimidines in water
|
Li, Qiao-Yan
|
|
|
16 |
3 |
p. 431-439
|
article
|
| 4 |
A novel and efficient one-pot four-component tandem approach for the synthesis of pyran derivatives
|
Zhang, Zhanyi
|
|
2012
|
16 |
3 |
p. 423-430
|
article
|
| 5 |
Applications of ortho-phenylisonitrile and ortho-N-Boc aniline for the two-step preparation of novel bis-heterocyclic chemotypes
|
Xu, Zhigang
|
|
2012
|
16 |
3 |
p. 607-612
|
article
|
| 6 |
A rational approach to selective pharmacophore designing: an innovative strategy for specific recognition of Gsk3β
|
Pradeep, H.
|
|
2012
|
16 |
3 |
p. 553-562
|
article
|
| 7 |
A rational approach to selective pharmacophore designing: an innovative strategy for specific recognition of Gsk3β
|
Pradeep, H.
|
|
|
16 |
3 |
p. 553-562
|
article
|
| 8 |
Consensus QSAR model for identifying novel H5N1 inhibitors
|
Sharma, Nitin
|
|
2012
|
16 |
3 |
p. 513-524
|
article
|
| 9 |
Exploring a sulfone linker utilizing trimethyl aluminum as a cleavage reagent: solid-phase synthesis of sulfonamides and ureas
|
Chung, Tsai-Wen
|
|
2012
|
16 |
3 |
p. 463-476
|
article
|
| 10 |
Focused enumeration and assessing the structural diversity of scaffold libraries: conformationally restricted bicyclic secondary diamines
|
Grygorenko, Oleksandr O.
|
|
2012
|
16 |
3 |
p. 477-487
|
article
|
| 11 |
In silico design of peptidic inhibitors targeting estrogen receptor alpha dimer interface
|
Chakraborty, Sandipan
|
|
2012
|
16 |
3 |
p. 441-451
|
article
|
| 12 |
Novel ionic liquid supported-multicomponent reaction toward chimeric bis-heterocycles
|
Chen, Chih-Hau
|
|
2012
|
16 |
3 |
p. 503-512
|
article
|
| 13 |
Rationalizing lead optimization by consensus 2D- CoMFA CoMSIA GRIND (3D) QSAR guided fragment hopping in search of γ-secretase inhibitors
|
Manoharan, Prabu
|
|
2012
|
16 |
3 |
p. 563-577
|
article
|
| 14 |
Reaction between enaminones and acetylenic esters in the presence of triphenylphosphine: a convenient synthesis of alkyl 2(1-benzyl-2,4-dioxo-2,3,4,5,6,7-hexahydro-1H-indol-3-yl)acetates
|
Nasiri, Farough
|
|
2012
|
16 |
3 |
p. 619-623
|
article
|
| 15 |
Regioselective multi-component synthesis of 1H-pyrazolo[3,4-d]pyrimidine-6(7H)-thiones
|
Safaei, Shirin
|
|
2012
|
16 |
3 |
p. 591-600
|
article
|
| 16 |
Sensitive electrospray mass spectrometry analysis of one-bead-one-compound peptide libraries labeled by quaternary ammonium salts
|
Bąchor, Remigiusz
|
|
2012
|
16 |
3 |
p. 613-618
|
article
|
| 17 |
Sustainable synthesis and automated deposition: an accessible discovery screening library of fragment-like purines
|
Kamper, Christoph
|
|
2012
|
16 |
3 |
p. 541-551
|
article
|
| 18 |
Syntheses of novel diaryl[d,f ][1,3]diazepines via one-pot Suzuki coupling followed by direct ring closure with carboxylic acids
|
Yan, Longjia
|
|
2012
|
16 |
3 |
p. 489-501
|
article
|
| 19 |
Synthesis and evaluation of functionalized indoles as antimycobacterial and anticancer agents
|
Cihan-Üstündağ, Gökçe
|
|
2012
|
16 |
3 |
p. 525-539
|
article
|
| 20 |
Synthesis of peptidomimetics, δ- and $${\varepsilon}$$-lactam tetrazoles
|
Gunawan, Steven
|
|
2012
|
16 |
3 |
p. 601-606
|
article
|
| 21 |
Ultrasound-promoted synthesis and immunosuppressive activity of novel quinazoline derivatives
|
Zhang, Lei
|
|
2012
|
16 |
3 |
p. 579-590
|
article
|
Journal description