Publications

  1. M.-S. Lin, T.-M. Hong, T.-H. Chou, S.-C. Yang, W.-C. Chung, C.-W. Weng,M.-L. Tsai, T.-J. Rachel Cheng, J.J.W. Chen, T.-C. Lee, C.-H. Wong, R.-J. Chein*, P.-C. Yang*, 4(1H)-quinolone derivatives overcome acquired resistance to anti-microtubule agents by targeting thecolchicine site of β-tubulin, European Journal of Medicinal Chemistry (2019). (10.1016/j.ejmech.2019.111584)

  2. Singam Naveen Kumar, Suhas Ravindra Bavikar, Chebolu Naga Sesha Sai Pavan Kumar, Isaac Furay Yu, Rong-Jie Chein* From Carbamate to Chalcone: Consecutive Anionic Fries Rearrangement, Anionic Si→C Alkyl Rearrangement and Claisen-Schmidt Condensation. Org. Lett. 2018, 20(17), pp5362-5366. (10.1021/acs.orglett.8b02269) Highlighted by Synfacts 2018, 14(11), 1180. (10.1055/s-0037-1611034)

  3. Hao-Wei Cheng, Rong-Jie Chein, Ting-Jen Cheng, Pei-Shan Wu, Hsin-Yi Wu, Pei-Fang Hung, Chia-Jen Wang, Yuan-Ling Hsu, Jau-Min Wong, Ang Yuan, Chi-Huey Wong, Pan-Chyr Yang, Szu-Hua Pan* 2-anilino-4-amino-5-aroylthiazole-type compound AS7128 inhibits lung cancer growth through decreased iASPP and p53 interaction. Cancer Sci. 2018, 109(3), pp 832-842. (10.1111/cas.13489)

  4. Singam Naveen Kumar, Isaac Furay Yu, Rong-Jie Chein* Oxathiaborolium: a Type of Chiral Lewis Acid Catalyst and Its Application in Catalytic and Highly Enantioselective Diels−Alder Reactions. Org. Lett. 201719(1), pp 22-25. (10.1021/acs.orglett.6b03147). Highlighted by C&EN 2017.

  5. Shih-Che Lin, Rong-Jie Chein* Total Synthesis of the Labdane Diterpenes Galanal A and Galanal B from Geraniol.  J. Org. Chem. 201782(3), pp 1575–1583. (10.1021/acs.joc.6b02766)

  6. Shang-Hua Wang, and Rong-Jie Chein* (Thiolan-2-yl)diphenylmethyl Benzyl Ether/N,N’-diarylurea Cocatalyzed Asymmetric Aziridination of Cinnamyl Bromide and Aryl Aldimine. TETRAHEDRON 2016, 72, 2607-2615. (10.1016/j.tet.2014.12.063)

  7. Chia-I Yen, Szu-Mam Liu, Wei-Shang Lo, Jhe-Wei Wu, Yi-Hsin Liu, Rong-Jie Chein, Renqiang Yang, Kevin C.-W. Wu, Jih Ru Hwu, Nianhan Ma,* Fa-Kuen Shieh* Cytotoxicityof Postmodified Zeolitic-Imidazolate Framework-90 (ZIF-90) Nanocrystals: Correlation between Functionality and Toxicity. CHEMISTRY-A EUROPEAN JOURNAL 2016, 22, 2925-2929. (10.1002/chem.201505005)

  8. Klim King*, Nai-Pin Lin, Yu-Hong Cheng, Gao-Hui Chen, Rong-Jie Chein* Isolation of Positive Modulator of Glucagon-like Peptide-1 Signaling from Trigonella foenum-graecum (Fenugreek) Seed. J. Biol. Chem. 2015290, 26235-26248. (10.1074/jbc.M115.672097)

  9. Darong Wang, Meiman Chen, Rong-Jie Chein, Wei-Min Ching, Chen-Hsiung Hung, Der-Lii M. Tzou* Cation ion specifically induces a conformational change in trans-dehydroandrosterone – A solid-state NMR study. STEROIDS 2015, 96, 73-80. (10.1016/j.steroids.2015.01.011)

  10. Chin-Yin Lin, Rong-Jie Chein* Lithiation of a Silyl Ether: Anionic Si→C Alkyl Migration. SYNLETT 2014, 25, 2827–2830. (10.1055/s-0034-1379493)

  11. Hong-Jay Lo, Chin-Yin Lin, Mei-Chun Tseng, and Rong-Jie Chein* Lithiation of a Silyl Ether; Formation on an ortho-Fries Hydroxyketone. Angew. Chem. Int. Ed. 2014, 53, 9026 –9029. (10.1002/anie.201404495)

  12. Chebolu Naga Sesha Sai Pavan Kumar, Rong-Jie Chein* Synthesis of Labdane Diterpenes Galanal A and B from (+)–Sclareolide. Org. Lett. 2014, 16, 2990−2992. (10.1021/ol501121v)

  13. Meng-Ting Huang, Hsin-Yi Wu, Rong-Jie Chein* Enantioselective Synthesis of Diaryl Aziridines Using Tetrahydrothiophene-Based Chiral Sulfides as Organocatalysts. Chem. Commun. 2014, 50, 1101-1103. (10.1039/C3CC47550F)

  14. Ravi Kumara Guralamatta Siddappa, Chih-Wei Chang, Rong-Jie Chein From Precursor to Catalyst: The Involvement of [Ru(ƞ5-Cp*)Cl2]2 in Highly Branch Selective Allylic Etherfication of Cinnamyl Chloride. TETRAHEDRON LETTERS 2014, 55, 1031-1035. (10.1016/j.tetlet.2013.12.074)

  15. Hsin-Yi Wu, Chih-Wei Chang, Rong-Jie Chein* Enantioselective Synthesis of (Thiolan-2-yl)diphenylmethanol and Its Application in Asymmetric, Catalytic Sulfur Ylide-Mediated Epoxidation. J. Org. Chem. 2013, 78, 5788-5793. (10.1021/jo400648f)

  16. Chih-Wei Chang, Rong-Jie Chein* The Absolute Configuration of Anti-HIV-1 Agent (-)-Concentricolide : Total Synthesis of (+)-(R)-Concentricolide. J. Org. Chem. 2011, 76, 4154-4157. (10.1021/jo2004132)

  17. Rong-Jie Chein, E. J. Corey* Strong Conformational Preferences of Heteroaromatic Ethers and Electron Pair Repulsion. Org. Lett. 2010, 12, 132-135. (10.1021/ol9025364)

  18. Rong-Jie Chein, Ying-Yeung Yeung and E. J. Corey* Highly Enantioselective Oxazaborolidine-Catalyzed Reduction of 1,3-Dicarbonyl Compounds: Role of the Additive Diethylaniline. Organic Letters 200911, 1611-1614. (10.1021/ol900258f)

  19. László Kürti, Rong-Jie Chein and E. J. Corey* Conformational Energetics of Cationic Backbone Rearrangements in Triterpenoid Biosynthesis Provide an Insight into Enzymatic Control of Product. J. Am. Chem. Soc. 2008130, 9031-9036. (10.1021/ja800980h)

  20. Ying-Yeung Yeung, Rong-Jie Chein, and E. J. Corey* Conversion of Torgov’s Synthesis of Estrone into a Highly Enantioselective and Efficient Process. J. Am. Chem. Soc. 2007129, 10346-10347. (10.1021/ja0742434)

  21. Tse-Lok Ho, Rong-Jie Chein Ritter Reaction of 1-Aryl-1-fluoro-2-haloethanes. J. Chin. Chem. Soc. 200653, 429-430. (10.1002/jccs.200600054)

  22. Tse-Lok Ho, Rong-Jie Chein Total Synthesis of (+)-β-Himachalene. Helv. Chim. Acta. 2006, 89, 231-239. (10.1002/hlca.200690025)

  23. Tse-Lok Ho, Rong-Jie Chein Unusual Thionation via Fragmentation. J. Chin. Chem. Soc. 200552, 1223-1225. (10.1002/jccs.200500176)

  24. Tse-Lok Ho, Rong-Jie Chein Intervention of Phenonium Ion in Ritter Reactions. J. Org. Chem. 200469, 591-592. (10.1021/jo035561y)

  25. Tse-Lok Ho*, Liang-Ren Kung, and Rong-Jie Chein Total Synthesis of (±)-2-Isocyanoallopupukeanane. J. Org. Chem. 200065, 5774-5779. (10.1021/jo000668w)

  26. Tse-Lok Ho*, and Rong-Jie Chein A Synthesis of 6-Myoporol. J. Nat. Prod. 199760, 493-494. (10.1021/np960704f)

  27. Tse-Lok Ho, Rong-Jie Chein Synthesis of (-)-Furodysinin from (+)-Limonene. Chem. Commun. 1996, 1147. (10.1039/CC9960001147)

Patents:

  1. R.O.C. I516474「良薑化合物及其類似物之合成」

  2. US patent US 9,193,665 B2 “Synthesis of Galanal Compounds and Analogues thereof”