Professor Shang-Shing P. Chou
Phone |
(O) 886 - 2 - 29052474 ( Lab)
886- 2- 29053583 (Fax) 886-2-29023209 |
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Experiences and honors: |
B.S., Fu Ph.D., The (Prof. Peter Smith) (1979) Postdoctoral Research Associate, The |
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Employment and
Services Associate
Professor, Fu Professor, Fu Jen Catholic University(1984-present) Chairman of the Chemistry Department (1986-1990) Dean
of the Dean of General Affairs (1996-2000) Director
of Holistic Vice President for Administration (2002-2003) Dean, Division of the Bachelor Program of Extension Education (2008-present) Awards and Honors Outstanding Teaching Award, Ministry of Education, R.O.C. 1992 Excellent Teaching Award, Fu Teaching Award, SVD Section of Fu Jen Catholic University, 1987, 1990-2002 Excellent Research Award, National Science Council, 1981-2000, 2002-2003 Excellent Research Award, Fu Research Award, SVD Section of Fu Jen Catholic University, 1989-2009 Best Research Paper of the Year, Journal of the Chinese Chemical Society, 1989 Excellent Teacher Award, Model Teacher Award, Association of Private Educational Institutions, R.O.C. 2001 Editor, Journal of the Chinese Chemical Society, 1989-present Member, Advisory Board of the Natural Science Division, National Science Council, 1991-1993, 1997-1998 Member, Committee for the Evaluation of Drug Precursors, Bureau of Food and Drug Analysis, Department of Health, Executive Yuan, R.O.C. 1998-present |
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Field |
Organic Chemistry、Materials Chemistry |
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Research Interests |
Organic Synthesis, Materials Chemistry, Heterocyclic Chemistry |
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Recent Publications |
1. Yih-Fong Liew, Chao-Tzu Huang, Shang-Shing P. Chou, Yuh-Chi Kuo, Shiu-Huey
Chou, Jyh-Yih Leu, Woan-Fang Tzeng, Su-Jane Wang,
Ming-Chi
Tang and Rwei-Fen Syu
Huang,* 2010, The Isolated and Combined Effects of Folic Acid and Synthetic Bioactive
Compounds against Aβ(25-35)-Induced Toxicity in Human Microglial Cells, Molecules, 15, 1632-1644. (SCI) IF
1.974 2. Shang-Shing
P. Chou* and Chih-Fen Liu, 2010, A Rapid, Solvent-Free Phase-Transfer Catalysis for N-Alkylation of Dihydropyridones
and Construction of the Indolizidine, Quinolizidine and
Pyridoazepeine Structures, J. Chin. Chem.
Soc. 57,
811-819. (SCI) IF 0.644 3. Shang-Shing P. Chou* and Yi-Lin Cai, 2011, Synthesis and Applications of Sulfur-Substituted cis-Hexahydro-2-quinolinones, Tetrahedron, 67, 1183-1186. (SCI) IF 2.983 4.
Tzu-Yu Lin, Cheng-Wei Lu, Shu-Kuei Huang, Shang-Shing P.
Chou, Yuh-Chi Kuo, Shiu-Huey Chou, Woan-Fang Tzeng, Chieh-Yih Leu, Rwei-Fen S. Huang, Yih-Fong Liew, Su-Jane Wang,* 2011, HTDP-2, a New Synthetic Compound, Inhibits Glutamate Release through
Reduction of Voltage-Dependent Ca 2+ Influx in Rat Cerebral Cortex Nerve Terminals, Pharmacology, 88, 1-2, 26-32. (SCI)
IF 1.603 5. Shang-Shing P. Chou,* Yi-Ching Chung, Po-An Chen, Shan-Lun Chiang, and Chien-Jung
Wu, 2011, Synthetic Applications of Sulfur-Substituted Indolizidines and Quinolizidines, J.
Org. Chem. 76, 692-695. (SCI) IF 3.818 6.
Shang-Shing P. Chou,* Tsung-Han Yang, Wan-Shiuan Wu,
and Tzu-Han Chiu, 2011, Stereospecific Synthesis of trans-5,6-Dihydropyridinones, Synthesis, 759-763. (SCI) IF
2.184 7.
Shang-Shing P. Chou,* Chien-Wen Huang, and Chih-Chun
Chang, 2011, Synthesis and Cycloaddition
Reactions of Sulfur-Substituted Quinolizidine Dienes, Tetrahedron, 67, 4505-4513. (SCI) IF 2.983 8.
Shang-Shing P.
Chou,* Bing-Heng Lee, Cheng-Han Ni,
Yu-Chou Lin, 2011, Synthesis and Reactions of sulfur-Substituted Indolizidinones,
Tetrahedron, 67, 5395-5401. (SCI) IF
2.983 9. Shang-Shing
P. Chou,* and Chien-Jhung J. Wu, 2012, Ring
Opening of Dihydro-2-pyridones and Intramolecular
Diels-Alder Reactions, Tetrahedron, 68,
1185-1191. (SCI) IF 3.060 10. Shang-Shing P. Chou,* Chang-Lin Lu and Yen-Hao Hsu, 2012,
Synthesis of Triazolyl-Substituted
Quinolizidine Imides, J. Chin. Chem. Soc. 59, 365-372. (SCI) IF 0.644 11. Shang-Shing P. Chou,* Jui-Chi Juan, Shwu-Chen Tsay, Kuei Pin Huang and Jih Ru
Hwu,* 2012,
Oxime Esters of 2,6-Diazaanthracene-9,10-dione and 4,5-Diazafluoren-9-one as Photo-induced
DNA-Cleaving Agents, Molecules, 17, 3370-3382. (SCI) IF 2.411 12. Shang-Shing P. Chou,* and Chien-Jhung
J. Wu, 2012, Chiral Synthesis of Indolizidines
209D and 167B via Asymmetric Oxidation of Sulfides and Sulfoxides, Tetrahedron, 68, 5025-5030. (SCI) IF 3.060 13. Shang-Shing
P. Chou,* Jhih-Liang Huang, 2012, Tandem cross metathesis and intramolecular aza-Michael
reaction to synthesize bicyclic piperidines and indolizidine
167E, Tetrahedron Lett.
53, 5552-5554. (SCI) IF2.588 14. Shang-Shing P. Chou,* Shan-Lun Chiang, Guan-Lin Huang, Bi-Shan Chiang, Ya-Chien Yu, 2013, New
Synthesis and Reactions of Indolizidine 167E and Indolizidine
Derivatives, Tetrahedron, 69, 274-283. (SCI) IF 3.060 15. Shang-Shing P. Chou,*
Jun-Wei Zhang, Kuan-Hua Chen, 2013, Synthetic Studies of Quinolizidine 195C and Derivatives, Tetrahedron, 69, 1499-1508. (SCI) IF 3.060 16. Shang-Shing P. Chou* and Jhih-Liang Huang, 2013, Studies toward
the First Stereoselective Total Synthesis of (±)-Quinolizidine 195C and Other Transformations, Molecules, 18,
8243-8256. (SCI) IF 2.679 17. Shang-Shing P. Chou* and Chao-Hsiang Kao, 2013, Synthetic Transformations of Sulfur-Substituted 4-Quinolizidinones, J. Chin. Chem. Soc. 60, 1260-1266. (SCI) IF 0.879 18. Jih Ru Hwu,* Shwu-Chen Tsay, Shih Chin Hong, Ming-Hua
Hsu,
Chih-Fen Liu, and Shang-Shing
P. Chou*, 2013, Relationship
Between Structure of Conjugated Oxime Esters and Their Ability to Cleave DNA, Bioconjugate Chem. 24, 1778−1783.
(SCI) IF 4.580 19. Jung-Sen
Liu, Fang Jung, Shih-Hsing Yang, Shang-Shing P. Chou, Jhih-Liang Huang, Chang-Lin Lu, Guan-Lin Huang,
Pan-Chyr Yang, Jau-Chen
Lin*, Guey-Mei Jow*, 2013,
FJU-C4, a New 2-Pyridone Compound, Attenuates Lipopolysaccharide-Induced Systemic
Inflammation via p38MAPK and NF-kB in Mice, Plos one, 8, e82877. (SCI)
IF 3.730 20. Shang-Shing P. Chou,* Kuo-Shiun Yang, and Tzu-Han Chiu, 2014,
Synthesis of the Precursors of Pumiliotoxin 251D and Awajanomycin
and Related Studies, Heterocycles, 89, 679-691. (SCI) IF 1.077 21. Shang-Shing P. Chou* and Wan-Shiuan Wu, 2014, Synthesis and reactions
of sulfur-substituted α,β-unsaturated δ-
and γ-lactones, Tetrahedron, 70, 1847-1854. (SCI) IF 3.060 |