近期论文
1. zhu d, wu y, wu b, luo b, ganesan a, pi r, wu f-h, huang p, wen s*. three-component pd/cu-catalyzed cascade reactions of cyclic iodoniums, alkynes, and boronic acids: an approach to methylidenefluorenes. organic letters 2014, online, doi: 10.1021/ol5006714.（if 6.14）
2. li m, luo b, liu q, hu y, ganesan a, huang p, wen s*. synthesis of n-acyl-n,o-acetals mediated by titanium ethoxide. org. lett. 2014, 16, 10-13.（if 6.14）
3. zhu d, liu q, luo b, chen m, pi r, huang p, wen s*. synthesis of carbazoles via one-pot copper-catalyzed amine insertion into cyclic diphenyleneiodoniums as a strategy to generate a drug-like chemical library. adv. synth. catal. 2013, 355, 2172-2178.（if 5.54）
4. zhu d, chen m, li m, luo b, zhao y, huang p, xue f, rapposelli a, pi r, wen s*. discovery of novel n-substituted carbazoles as neuroprotective agents with potent anti-oxidative activity. eur. j. med. chem. 2013, 68, 81-88.（if 3.50）
5. guan r, xu x, chen m, hu h, ge h, wen s*, zhou s, pi r. advances in the studies of roles of rho/rho-kinase in diseases and the development of its inhibitors. eur. j. med. chem. 2013, 70, 613-622.（if 3.50）
6. wen s, zhu d, huang p. targeting cancer cell mitochondria as a therapeutic approach, future med. chem., 2013, 5(1):53-67.（if 3.31）
7. zhou b, zuo y, li b, wang h, liu h, wang x, qiu x, hu y, wen s, du j, bu x. deubiquitinase inhibition of 19s regulatory particles by 4-arylidene curcumin analogue ac17 causes nf-κb inhibition and p53 reactivation in human lung cancer cells. mol cancer ther. 2013, 12(8):1381-92.（if 5.23）
8. li x, lu w, hu y, wen s, qian c, wu w, huang p. effective inhibition of nasopharyngeal carcinoma in vitro and in vivo by targeting glycolysis with oxamate. int. j. oncol. 2013, 43(5): 1710-1718.（if 2.40）
9. abrahams gl, kumar a, savvi s, hung aw, wen s, abell c, barry ce 3rd, sherman dr, boshoff hi, mizrahi v. pathway-selective sensitization of mycobacterium tuberculosis for target-based whole-cell screening. chem biol. 2012, 27, 19(7), 844-54.（if 5.83）
10. tiffon, c., adams, j., van der fits, l., wen, s., townsend, p., ganesan, a., hodges, e., vermeer, m., packham, g. the histone deacetylase inhibitors vorinostat and istodax downmodulate il10 expression in cutaneous t-cell lymphoma cells british journal of pharmacology, 2011, 162, 1590-1602.（if 4.41）
11. hung, a.w., silvestre, h.l., wen, s., ciulli, a., blundell, t.l., abell, c. application of fragment growing and fragment linking to the discovery of novel inhibitors of mycobacterium tuberculosis pantothenate synthetase angew. chem. int. ed. 2009, 48, 8452-8456.（if 13.46）
12. heikkila, t.j., surade, s., silvestre, h.l., dias, m.v.b., ciulli, a., bromfield, k., scott, d., howard, n., wen, s., wei, a.h., osborne, d., abell, c., blundell, t.l. fragment-based drug discovery in academia: experiences from a tuberculosis programme nato security through science series c: environmental security, 2009, 21-36.
13. wen, s., packham, g., ganesan, a., macrolactamization versus macrolactonization: total synthesis of fk228, the depsipeptide histone deacetylase inhibitor j org chem, 2008, 73, 9353-9361.（if 4.56）
14. wen, s., carey, k., nakao, y., fusetani, n., packham, g., ganesan, a., total synthesis of azumamide a and azumamide e, evaluation as histone deactylase inhibitors, and design of a more potent analogue organic letters 2007, 9 (6), 1105-1108. （if 6.14）
15. yurek-george, a., cecil, a., mo, a.h.k., wen, s., rogers, h., maeda, s., yoshida, m., packham, g., ganesan, a., the first biologically active synthetic analogues of fk228, the depsipeptide histone deacetylase inhibitor, j. med. chem., 2007; 50(23); 5720-5726.（if 5.61）
16. wen, s.-j., hu, t.-s., yao, z.-j., macrocylization studies and total synthesis of cyclomarin c, an anti-inflammatory marine cyclopeptide, tetrahedron, 2005, 61 (21), 4931-4938.（if 2.80）
17. wen, s.-j., yao, z.-j., total synthesis of cyclomarin c. organic letters 2004, 6 (16) 2721-2724.（if 6.14）
18. wen, s.-j.; zhang, h.-w.; yao, z.-j. synthesis of a fully protected (2s, 3r)-n-(1',1'-dimethyl-2'- propenyl)-3-hydroxy-tryptophan from tryptophan tetrahedron lett. 2002, 43 (30) 5291-5294.（if 2.40）
