姓 名:刘峰
职称职务:教授
联系电话:0512-65882569
电子邮箱:fliu2@suda.edu.cn
办公地址:苏州市工业园区仁爱路199号药学院云轩楼1434
个人简介:
一、学习工作经历
2012.9— 至今:副教授,教授,www.优德88.cpm 医学部药学院
2009.5— 2012.8:博士后研究助理,北卡罗来纳大学教堂山分校药学院
2009.1—2009.5;助理研究员,中科院上海有机所
2003.9— 2009.1:研究生,中科院上海有机所
1999.9— 2003.7:本科, 厦门大学化学系
二、研究方向
(1)表观遗传蛋白小分子调控剂的设计与合成
(2)神经疾病和癌症的“靶向治疗”药物研发
(3)有机合成新方法在药物研发中的应用
三、主要学术科研成果
先后主持国家自然科学基金、江苏省自然科学基金等项目十余项,曾参与国家自然科学基金重点项目、美国NCI、NIH、美国国防部等项目研究;在Nat. Chem. Biol.、Chem、J. Med. Chem.、Org. Lett.和Chem. Commun.等学术期刊上发表SCI论文80余篇。
(论文引用见:http://scholar.google.com/citations?user=h_j1fQYAAAAJ&hl=en)
2025
84) Tan, G.-Q.; Zhou, Q.-L.; Qin, H.-T.; Liu, F.* Access to 5-to 14-Membered N‑Heterocycles by Alkylamination of 1,3-Dienes via Palladium Catalysis. Org. Lett.2025, DOI: 10.1021/acs.orglett.5c00508.
2024
83) Ling, T.-P.; Qin, H.-T.;* Liu, F.* Recent Advances in Enantioselective Radical Reactions of C(sp3)–H Bond. Chin. J. Org. Chem.2024, DOI:10.6023/cjoc202406042.
82) Gaolei Zuo, Haojie Xu, Yaobin Zhang, Zhi Liu, Jinyue Tu, Donghui Gou, Peng Fu, Haifeng Huang, Jianhua Ren, Yuanyuan Hu, Feng Liu*, Jie Jack Li*, Guiping Zhang*, Development of a Practical Telescoped Process to Prepare (P)-7-(2-Amino-6-fluorophenyl)-4-hydroxy-6-(trifluoromethyl)pyrido[3,4-d]pyrimidin-8(7H)-one: a Key Intermediate of KRASG12C Inhibitor GH35. Org. Process Res. Dev.2024, 28(10), 3871–3882. DOI: 10.1021/acs.oprd.4c00279.
81) Ke-Dong Xu, Xing-Yu Gong, Meng Li, Lin Yi, Hai-Tao Qin, Feng Liu*,N-Directed, Radical Relay Enantioconvergent Sulfinylation of Distal C(sp3)-H Bonds via Cobalt Catalysis. Org. Lett.2024, 26, 8999-9004. DOI: 10.1021/acs.orglett.4c03094.
80) Chen, Y.-T.; Jiang, H.-Q.; Sun, Z.-B.; Liu, F.* andSu, M.*Hydantoin derivative dimers as broad-spectrum antimicrobial agents against ESKAPE pathogens with enhanced killing rate and stability. RSC Med. Chem.2024,15, 2340-2350.DOI: 10.1039/d4md00374h.
79) Tan, G.-Q.; Xu, K.-D.; Qin, H.-T.; Liu, F;*Nitrogen-directed unactivated γ-C(sp3)–H functionalization of amides toward 7-membered lactones via photoredox catalysis. Org. Chem. Front. 2024,11, 3724 – 3728. DOI: 10.1039/D4QO00564C.
78) Yang, J.-W.; Li, M.; Tan, G.-Q.; Liu, F;* Qin, H.-T.*N-Directed defluorinative γ-C(sp3)−H allylation of sulfamate esters for synthesis of gem-difluoroalkenes via photoredox catalysis. Eur.J. Org. Chem.2024,27, e202400011. DOI: 10.1002/ejoc.202400011.
2023
77) Chen, Y.-T.; Ye, Z.-F.; Zhen, W.-T.; Zhang, L.; Min, X.-Y.; Wang, Y.-P. *; Liu, F.* andSu, M.* Design and Synthesis of Broad-spectrum Antimicrobial Amphiphilic Peptidomimetics to Combat Drug-resistance, Bioorg. Chem.2023, 140:106766. DOI: 10.1016/j.bioorg.2023.106766
76) Xu, K.-D.; Yang, J. W.; Qin, H.-T.; Liu, F.* Amidyl Radical Directed γ-C(sp3)–H Functionalization with Silyl Enol Ethers via Photoredox Catalysis, Eur.J. Org. Chem.2023, e202300543.DOI: 10.1002/ejoc.202300543
75) Wu, H.; He, S.-H.; Qin, H.-T.; Liu, F.* “Photoredox-catalyzed, oxygen-directed unactivated γ-C(sp3)–H functionalization toward oxepanes” Org. Chem. Front. 2023, 10, 3870-3874.DOI: 10.1039/D3QO00689A
74) He, S.-H.; Chen, G.-L.; Gong, X.-Y.; Ao, G.-Z.; Liu, F.* “Catalytic Decarboxylative Radical Sulfinylation” J. Org. Chem.2023, 88(11), 6671-6681.DOI: 10.1021/acs.joc.2c03051
73) Ma Su, Zhang Li, Duanyang Yan, Xingyue Ji* and Feng Liu* “Chemical Strategies Toward Prodrugs And Fluorescent Probes For Gasotransmitters” Mini-Reviews In Medicinal Chemistry, 2024, 24(3), 300-329. DOI: 10.2174/1389557523666230427152234.
2022
72) Yang, J.-W.; Tan, G.-Q.; Liang, K.-C.; Xu, K.-D.; Su, M.; Liu, F.* “Copper-Catalyzed, N-Directed Distal C(sp3)-H Functionalization toward Azepanes” Org. Lett.2022,24(42), 7796-7800. DOI: 10.1021/acs.orglett.2c03135.
71) Tang, W.; Yan, D.-Y.; Liang, K.-C.; Su, M.*;Liu, F.* “Radical-mediated alkene carboamination/dearomatization of arylsulfonyl-o-allylanilines via photoredox catalysis”Org. Chem. Front.2022,9(23), 6535-6539. DOI: 10.1039/D2QO01221A.
70) Fang, J.; Min, Q.-Q.; Qin, H.-T.*Liu, F.*“Intermolecular Acylation with Acylphosphonates as Alkyl Radical Receptor Under Metal-Free Conditions”Chin. J. Org. Chem.2022,42(12), 4332-4339. DOI: 10.6023/cjoc202207044. (三区,方晶, 闵庆强, 秦海涛, 刘峰,无金属条件下以酰基膦酸酯为烷基自由基受体的分子间酰化反应,有机化学)
69)Tu, J.-L.; Tang, W.; He, S.-H.; Su, M.;Liu, F.*“Acceptorless dehydrogenative amination of alkenes for the synthesis of N-heterocycles”Sci. China. Chem.2022, 65(7), 1330-1337.Doi: 10.1007/s11426-022-1241-x.
2021
68) Chen, G.-L.; He, S.-H.; Cheng, L.*; Liu, F.* “Copper-Catalyzed N-Directed Distal C(sp3)-H Sulfonylation and Thiolation with Sulfinate Salts” Org. Lett.2021, 23(21), 8338-8342.DOI: 10.1021/acs.orglett.1c03075
67) Tu, J.-L.; Yang, J.-W.; Xu, W.; Su, M.;Liu, F.* “Amidyl radical-mediated aminodifluoroallylation of alkenes via photoredox catalysis”Org. Chem. Front.2021, 8(22), 6405–6410. DOI: 10.1039/D1QO01208H
66) Tu, J.-L.; Tang, W.;Liu, F.*“Photoredox-Neutral Alkene Aminoarylation for the Synthesis of 1,4,5,6-Tetrahydropyridazines”Org. Chem. Front.2021,8(14), 3712 – 3717. DOI: 10.1039/D1QO00325A
65) Zhu, Z.-F.; Chen, G.-L.;Liu, F.*“Ruthenium-catalysed meta-selective CAr–H bond alkylation via deaminative strategy”Chem. Commun.2021,57(27), 3411-3414. DOI: 10.1039/D1CC00039J.
64) Su, M.; Gong, X.-Y.;Liu, F.*“An update on the emerging approaches for histone deacetylase (HDAC) inhibitor drug discovery and future perspectives”Expert Opinion on Drug Discovery2021,16(7), 745-761. DOI: 10.1080/17460441.2021.1877656.
63) Tu, J.-L.; Tang, W.; Xu, W.;Liu, F.*“Iminyl Radical-Promoted C-C Bond Cleavage/Heck-Like Coupling via Dual Cobaloxime and Photoredox Catalysis”The Journal of Organic Chemistry2021,86(3), 2929-2940. DOI: 10.1021/acs.joc.0c02834
62) Min, Q.-Q.; Yang, J.-W.; Pang, M.-J.; Ao, G.-Z.*;Liu, F.*“Copper-catalyzed, N-directed remote C(sp3)-H azidation and thiocyanation”Org. Chem. Front.2021,8(2), 249-253. DOI: 10.1039/D0QO01012J.
61) Su, M. Wang, W.;Liu, F.*; Li H.* “Recent progress on the discovery of NLRP3 inhibitors and their therapeutic potential”Current Medicinal Chemistry2021,28(3), 569-582. DOI:10.2174/0929867327666200123093544.
2020
60)Liu, J.-L.;Tu, J.-L.;Liu, F.* “Visible-Light-Promoted Intramolecularα-Allylation of Aldehydes in the Absence of Sacrificial Hydrogen Acceptors”Org. Lett.2020,22, 7369-7372. DOI: 10.1021/acs.orglett.0c02742
59) Qiu, Y. Huang, L.; Fu, J.; Han, C.; Fang, J.; Liao, P.; Chen, Z.; Mo, Y.; Sun, P.; Liao, D.; Yang, L.; Wang, J.; Zhang, Q.; Liu, J.;Liu, F.; Liu, T.; Huang, W.; Yang, H.; Jiang, R. “TREK Channel Family Activator with a Well-Defined Structure-Activation Relationship for Pain and Neurogenic Inflammation”Journal of Medicinal Chemistry2020,63, 3665-3677.DOI: 10.1021/acs.jmedchem.9b02163.
58) Min, Q.-Q.; Yang, J.-W.; Pang, M.-J.; Ao, G.-Z.*;Liu, F.*“Copper-Catalyzed Remote C(sp3)-H Amination of Carboxamides”Org. Lett.2020,22, 2828-2832. DOI: 10.1021/acs.orglett.0c00829.
57) He, J.; Chen, G.; Zhang, B.; Li, Y.; Chen, J.-R.; Xiao, W.-J.;Liu, F.*; Li, C.* “Catalytic Decarboxylative Radical Sulfonylation”Chem2020,6, 1149-1159. DOI: 10.1016/j.chempr.2020.02.003.
56) Tu, J.-L.;Liu, J.-L.;Tang, W.; Su, M.;Liu, F.*“Radical Aza-Cyclization ofa-Imino-oxy Acids for Synthesis of Alkene-Containing N-Heterocycles via Dual Cobaloxime and Photoredox catalysis”Org. Lett.2020,22, 1222-1226. DOI:10.1021/acs.orglett.0c00224.
55) Zhang, M. M.; Li, S.-H.; Tu, J.-L.; Min, Q.-Q.;Liu, F.*“Metal-free iminyl radical-mediated C-C single bond cleavage/functionalization of redox-active oxime esters”Org. Chem. Front.2020,7, 622-627. DOI: 10.1039/c9qo01446b
2019
54) Zhao, Y.; Li, S.-H.; Zhang, M.-M.;Liu, F.*“Synthesis of β,γ-Unsaturated Esters and γ-Ketone Esters with Amino Acid Ester-Derived Katritzky Salts”Acta Chimica Sinica(化学学报)2019,77(9), 916-921. DOI: 10.6023/A19040121
53) Zhu, Z.-F.; Tu, J.-L.;Liu, F.*“Ni-Catalyzed Deaminative Hydroalkylation of Internal Alkynes”Chem. Commun.2019,55, 11478 – 11481. DOI: 10.1039/C9CC05385A.
52) Shen, W.-G.; Wu, Q.-Y.; Gong, X.-Y.; Ao, G.-Z.;Liu, F.*“A facile method for hydroxytrifluoromethylation of alkenes with Langlois reagent and DMSO”Green Chem.2019,21, 2983 – 2987. DOI: 10.1039/C9GC00886A.
51) Christopher J. MacNevin, Takashi Watanabe, Matthew Weitzman, Akash Gulyani, Sheryl Fuehrer, Nicholas K. Pinkin, Xu Tian,Feng Liu, Jian Jin, and Klaus M. Hahn, “Membrane-Permeant, Environment-Sensitive Dyes Generate Biosensors within Living Cells”J. Am. Chem. Soc.2019, 10.1021/jacs.8b09841.
50) Li, B.; Mao, Q.; Zhou, J.;Liu, F.; Ye, N.* “HFIP-promoted Michael reactions: direct para-selective C–H activation of anilines with maleimides”Org. Biomol. Chem.2019,17, 2242-2246.
49) Min, Q.-Q.; Li, N.; Chen, G.-L.;Liu, F.*“Copper-catalysed C(sp3)–N coupling initiated by selective C–C bond cleavage of cyclobutanone oxime esters”Org. Chem. Front.2019,6, 1200-1204. DOI: 10.1039/C9QO00235A.
48) Zhu, Z.-F.; Zhang, M.-M.;Liu, F.*“Radical alkylation of isocyanides with amino acid-/peptide-derived Katritzky salts via photoredox catalysis”Org. Biomol. Chem.2019,17, 1531-1534.DOI: 10.1039/C8OB02786B.
2018
43) Xu, X.; Min, Q.-Q.; Li, N.;Liu, F.*“Visible light-promoted umpolung coupling of aryl tri-/difluoroethanones with 2-alkenylpyridines”Chem. Commun.2018,54, 11017-11020. DOI: 10.1039/C8CC06748A
42) Wu, Q.-Y.;Min, Q.-Q.; Ao, G.-Z.*;Liu, F.* “Radical alkylation of para-quinone methides with 4-substituted Hantzsch esters/nitriles via organic photoredox catalysis”Org. Biomol. Chem.2018,16, 6391-6394. DOI:10.1039/C8OB01641K.
41)Liu, J.-L.;Wu, S.-W.;Wu, Q.-Y.;Liu, F.*Diverse Transformation of Vinyl Azides with 2,2,6,6-Tetramethyl-N-oxopiperidinium.J. Org. Chem.2018,83, 8183-8192. DOI: 10.1021/acs.joc.8b00954.
40) Wu, Q.-Y.;Ao, G.-Z.*;Liu, F.*Redox-neutral tri-/difluoromethylation ofpara-quinone methides with sodium sulfinates.Org. Chem. Front.2018,5, 2061-2064. DOI: 10.1039/C8QO00428E.
39) Kaniskan, H. Ü.; Eram, M. S.; Zhao, K.; Szewczyk, M. M.; Yang, X.; Schmidt, K.; Luo, X.; Xiao, S.; Dai, M.; He, F.; Zang, I.; Lin, Y.; Li, F.; Dobrovetsky, E.; Smil, D.; Min, S.-J.; Lin-Jones, J.; Schapira, M.; Atadja, P.; Li, E.; Barsyte-Lovejoy, D.; Arrowsmith, C. H.; Brown, P. J.;Liu, F.*; Yu, Z.*; Vedadi, M.*; Jin, J.* Discovery of Potent and Selective Allosteric Inhibitors of Protein Arginine Methyltransferase 3 (PRMT3).Journal of Medicinal Chemistry2018,61, 1204-1217. DOI: 10.1021/acs.jmedchem.7b01674. PMID:29244490
38)Babault, N.; Allali-Hassani, A.; Li, F.; Fan, J.; Yue, A.; Ju, K.;Liu, F.*; Vedadi, M.*; Liu, J.*; Jin, J.* “Discovery of Bisubstrate Inhibitors of NicotinamideN-Methyltransferase (NNMT)”Journal of Medicinal Chemistry2018,61, 1541-1551.DOI: 10.1021/acs.jmedchem.7b01422.
37)Liu, J.-L.; Zhu, Z.-F.;Liu, F.*“Oxycyanation of Vinyl Ethers with 2,2,6,6-Tetramethyl-N-oxopiperidinium Enabled by Electron Donor-Acceptor Complex”Org. Lett.2018,20,720-723.
36)Zhao, Y.;Liu, F.*“Recent advance in radical fluoroalkylation with sulfinate salts”Tetrahedron Lett.2018,59, 180-187. DOI: 10.1016/j.tetlet.2017.12.022
2017
35)Wu, S.-W.; Liu, J.-L.;Liu, F.*“cis-Specific cyanofluorination of vinyl azides enabled by electron-donor-acceptor complexes: synthesis ofa-azido-ß-fluoronitriles”Chem. Commun.2017,53, 12321-12324. DOI: 10.1039/C7CC07165E.
34) Xu, X.;Liu, F.* “Transition-metal-free radical tri-/difluoromethylation ofN,N-dialkylhydrazones with sodium sulfinates”Org. Chem. Front.2017,4, 2306-2310. DOI: 10.1039/C7QO00635G
33) Fang, J.;Shen, W.-G.; Ao, G.-Z.*;Liu, F.*“Transition-metal-free radical fluoroalkylation of isocyanides for the synthesis of tri-/di-/monofluoromethylated phenanthridines”Org. Chem. Front.2017,4, 2049-2053. DOI: 10.1039/C7QO00473G
32) Fang, J.; Wang, Z.-K.;Wu, S.-W.; Shen, W.-G.; Ao, G.-Z.;Liu, F.* “Photoredox-catalysed chloro-, bromo- and trifluoromethylthiotrifluoromethylation of unactivated alkenes with sodium triflinate”Chem. Commun.2017,53, 7638-7641.DOI:10.1039/C7CC01903C.
31) Qin, H.-T.; Xu, X.;Liu, F.*“Aerobic Oxidation of Alkynes into 1,2-Diketones via Organic Photoredox Catalysis”ChemCatChem2017,9, 1409-1412. DOI: 10.1002/cctc.201700061
30) Qin, H.-T.; Wu, S.-W.; Liu, J.-L.;Liu, F.*“Photoredox-Catalysed Redox-Neutral Trifluoromethylation of Vinyl Azides for the Synthesis of a–Trifluoromethylated Ketones”Chem. Commun.2017,53, 1696-1699.
29) Qin, H.-T.; Li, H.-Q.;*Liu, F.*“Selective histone deacetylase small molecule inhibitors: recent progress and perspectives”Expert Opin. Ther. Pat.2017,27, 621-636. DOI: 10.1080/13543776.2017.1276565
2016
28) Wu, S.-W.;Liu, F.*“Synthesis ofα-Fluoroketones from Vinyl Azides and Mechanism Interrogation”Org. Lett.2016,18, 3642-3645.
2015
23) Shi, D.; Qin, H.;Zhu, C;* Liu, F.*“Selectfluor–Bu4NI-Mediated C(sp3)–H Oxidation in Aqueous Media: Synthesis ofΔ2-Isoxazolines from Oximes”Eur.J. Org. Chem.2015,5084-5088. DOI: 10.1002/ejoc.201500780
22) Wang, L.; Xie, L.; Ramachandran, S.; Lee, Y.; Yan, Z.; Zhou, L.; Krajewski, K.;Liu, F.; Zhu, C.; Chen, David J.; Strahl, Brian D.; Jin, J.; Dokholyan, Nikolay V.; Chen, X.“Non-canonical Bromodomain within DNA-PKcs Promotes DNA Damage Response and Radioresistance through Recognizing an IR-Induced Acetyl-Lysine on H2AX”Chem. Biol.2015,22, 7, 849-861. DOI: 10.1016/j.chembiol.2015.05.014.
21) Zhang, Z.;Liu, F.*“CuX2-mediated oxybromination/aminochlorination of unsaturated amides: synthesis of iminolactones and lactams”Org. Biomol. Chem.2015,13, 6690-6693.DOI: 10.1039/c5ob00520e
20)Dong, K.; Qin, H.;Liu, F.*; Zhu, C.*“Oxime-Mediated Oxychlorination and Oxybromination of Unactivated Olefins”Eur.J. Org. Chem.2015,1419-1422. DOI: 10.1002/ejoc.201403538
2014
17)Sundriyal, S.;Malmquist, N. A.;Caron, J.;Blundell, S.;Liu, F.;Chen, X.;Srimongkolpithak, N.;Jin, J.;Charman, S. A.;Scherf, A.;Fuchter, M. J. “Development of Diaminoquinazoline Histone Lysine Methyltransferase Inhibitors as Potent Blood-Stage Antimalarial Compounds”ChemMedChem,2014,9, 2360-2373.
16)Lehnertz, B.;Pabst, C.;Su, L.;Miller, M.;Liu, F.;Yi, L.;Zhang, R.,Krosl, J.,Yung, E.,Kirschner, J.,Rosten, P.,Underhill, T. M.,Jin, J.,Hébert, J.,Sauvageau, G.,Humphries, R. K.,Rossi, F. M. “The methyltransferase G9a regulates HoxA9-dependent transcription in AML”Genes Dev.2014,28,317-327.
14)Liu, F.*; Li. C. “Total synthesis of (S)-14-azacamptothecin”,Org. Biomol. Chem.2014,12, 637-642.
2013
13)Liu, F.; Barsyte-Lovejoy, D.; Li, F.; Xiong, Y.; Korboukh, V.; Huang, X. P.; Allali-Hassani, A.; Janzen, W. P.; Roth, B. L.; Frye, S. V.; Arrowsmith, C. H.; Brown, P. J.; Vedadi, M.; Jin, J. “Discovery of an in vivo Chemical Probe of the Lysine Methyltransferases G9a and GLP”J. Med. Chem.2013,56, 8931-8942.
12) Konze, K. D.; Ma, A.; Li, F.; Barsyte-Lovejoy, D.; Parton, T.; MacNevin, C. J.;Liu, F.; Gao, C.; Huang, X. P.; Kuznetsova, E.; Rougie, M.; Jiang, A.; Pattenden, S. G.; Norris, J. L.; James, L. I.; Roth, B. L.; Brown, P. J.; Frye, S. V.; Arrowsmith, C. H.; Hahn, K. M.; Wang, G. G.; Vedadi, M.; Jin, J. “An Orally Bioavailable Chemical Probe of the Lysine Methyltransferases EZH2 and EZH1”,ACS Chemical Biology,2013,8, 1324-1334.
11)Liu, F.;Li, F.; Ma, A.; Dobrovetsky, E.; Dong, A.; Gao, C.; Korboukh, I.; Liu, J.; Smil, D.; Brown, P. J.; Frye, S. V.; Arrowsmith, C. H.; Schapira, M.; Vedadi, M.; Jin, J. “Exploiting an Allosteric Binding Site of PRMT3 Yields Potent and Selective Inhibitors”J. Med. Chem.2013,56, 2110-2124.
Before 2013
10)Siarheyeva, A.; Senisterra, G.; Allali-Hassani, A.; Dong, A.; Dobrovetsky, E.; Wasney, Gregory A.; Chau, I.; Marcellus, R.; Hajian, T.;Liu, F.; Korboukh, I.; Smil, D.; Bolshan, Y.; Min, J.; Wu, H.; Zeng, H.; Loppnau, P.; Poda, G.; Griffin, C.; Aman, A.; Brown, Peter J.; Jin, J.; Al-awar, R.; Arrowsmith, Cheryl H.; Schapira, M.; Vedadi, M. "An Allosteric Inhibitor of Protein Arginine Methyltransferase 3"Structure2012,20, 1425-1435.
9)Liu, F.; Barsyte-Lovejoy, D.; Allali-Hassani, A.; He, Y.; Herold, J. M.; Chen, X.; Yates, C. M.; Frye, S. V.; Brown, P. J.; Huang, J.; Arrowsmith, C. H.; Jin, J. “Optimization of Cellular Activity of G9a Inhibitors 7-Aminoalkoxy-quinazolines”.J. Med. Chem.2011,54, 6139-6150.
8)Yost, J. M.; Korboukh, I.;Liu, F.; Gao, C.; Jin, J. “Targets in Epigenetics: Inhibiting the Methyl Writers of the Histone Code”.Curr.Chem.Genomics2011,5, 72-84. (共同第一作)
7)Vedadi, M#.; Barsyte-Lovejoy, D#.;Liu, F#.; Rival-Gervier, S.; Allali-Hassani, A.; Labrie, V.; Wigle, T. J.; DiMaggio, P. A.; Wasney, G. A.; Siarheyeva, A.; Dong, A.; Tempel, W.; Wang, S.-C.; Chen, X.; Chau, I.; Mangano, T.; Huang, X.-P.; Simpson, C. D.; Pattenden, S. G.; Norris, J. L.; Kireev, D. B.; Tripathy, A.; Edwards, A.; Roth, B. L.; Janzen, W. P.; Garcia, B. A.; Petronis, A.; Ellis, J.; Brown, P. J.; Frye, S. V.; Arrowsmith, C. H.; Jin, J. “A Chemical Probe Selectively Inhibits G9a and GLP Methyltransferase Activity in Cells”.Nature Chem. Biol.2011,7, 566-574. (共同第一作,Highlighted by News and Views:Nature Chemical Biology, 2011, 7, 499-500 and SciBX, 2011, 4(31), doi:10.1038/scibx.2011.890)
6)Liu, F.; Chen, X.; Allali-Hassani, A.; Quinn, A. M.; Wigle, T. J.; Wasney, G. A.; Dong, A.; Senisterra, G.; Chau, I.; Siarheyeva, A.; Norris, J. L.; Kireev, D. B.; Jadhav, A.; Herold, J. M.; Janzen, W. P.; Arrowsmith, C. H.; Frye, S. V.; Brown, P. J.; Simeonov, A.; Vedadi, M.; Jin, J. “Protein Lysine Methyltransferase G9a Inhibitors: Design, Synthesis, and Structure Activity Relationships of 2,4-Diamino-7-aminoalkoxy-quinazolines”.J. Med. Chem.2010,53, 5844-5857.
5)Liu, F.; Chen, X.; Allali-Hassani, A.; Quinn, A. M.; Wasney, G. A.; Dong, A.; Barsyte, D.; Kozieradzki, I.; Senisterra, G.; Chau, I.; Siarheyeva, A.; Kireev, D. B.; Jadhav, A.; Herold, J. M.; Frye, S. V.; Arrowsmith, C. H.; Brown, P. J.; Simeonov, A.; Vedadi, M.; Jin, J. “Discovery of a 2,4-Diamino-7-aminoalkoxyquinazoline as a Potent and Selective Inhibitor of Histone Lysine Methyltransferase G9a”.J. Med. Chem.2009,52, 7950-7953.
4)Ju, Y.;Liu, F.; Li. C. “Palladium-Catalyzed Sequential Cyanation/N-Addition/ N-Arylation in One-Pot: Efficient Synthesis of Luotonin A and Its Derivatives”.Org. Lett.2009,11, 3582-3585.
3)Liu, F.; Li. C. “Intramolecular Formal [4 + 2] Cycloaddition of Nitriles with Amides Triggered by TMSOTf/Et3N: Highly Efficient Construction of Pyrrolo[1,2-a]pyrimidin-4(6H)-ones”.J. Org. Chem.2009,74, 5699-5702.
2)Liu, F.; Liu, K.; Yuan, X.; Li. C. “5-Exo versus 6-Endo Cyclization of Primary Aminyl Radicals: An Experimental and Theoretical Investigation”.J. Org. Chem.2007,72, 10231-10234.
1)Zhan, Z.; Lang, K.;Liu, F.; Hu, L. “Water Effects on SmI2Reductions: A Novel Method for the Synthesis of Alkyl Thiols by SmI2-Promoted Reductions of Sodium Alkyl Thiosulfates and Alkyl Thiocyanates”.Syn. Commun.2004,34, 3203.