楊德芳特聘教授

學士 逢甲大學化學工程系學士 (1980)
碩士 美國德州大學化學系碩士 (1986)
博士 美國紐約州立大學化學系博士 (1991)
美國麻省大學博士後研究員 (1991-1992)
美國喬治亞大學博士後研究員 (1992-1994)
美國紐約安卓生化公司研究員(1994-1996)
朝陽科技大學應用化學系副教授 (1996-2008)
國立暨南國際大學應用化學系副教授 (2008-2012)
國立暨南國際大學應用化學系教授 (2012-)

1.    樟腦分子衍生物的重排反應與合成
2.    有機掌性催化劑
3.    有機不對稱反應
4.    新穎雜環化合物合成
5.    天然有機化合物合成
6.    有機材料合成

(1)   Sheng-Han Huang, Yu-Wei Shih, Wen-Tse Huang, Deng-Hong Li, Te-Fang Yang*, “Tendem additions of  3,4-dihydroisoquinolines to g-hydroxy-a,b-unsaturated ketones: a green and new access to oxazolo[2,3-a]tetrahydroisoquinolines”, RSC Advances, 2016, 6, 91870-91874. (SCI). 
(2)   Te-Fang Yang, Sheng-Han Huang, Yi-Pang Chiu, Bo-Hsiang Chen, Yu-Wei Shih, Yu-Chang Chang, Jie-Yi Yao, Yao-Jen Lee, Ming-Yu Kuo, “ Pyromellitic dithioimides: thionation improves air-stability and electron mobility of N-type organic field-effect transistors”, Chem Commun, 2015, 51, 13772-13775. 
(3)   Somnath Mondal, Wei-Hsiang Lin, Yu-Chi Chen, Sheng-Han Huang, Rong Yang, Bo-Hsiang Chen, Te-Fang Yang*, Shih-Wei Mao*, Ming-Yu Kuo* , “Solution-processed single-crystal perylene diimide transistors with high electron mobility”, Organic Electronics, 2015, 23, 64-69. (SCI). 
(4)   Hsu-Chun Cheng, Kuo Yuan Chiu, Shih Hua Lu, Ching-Chin Chen, Yen Wei Lee, Te-Fang Yang*, Ming Yu  Kuo*, Peter Ping-Yu Chen*, Yuhlong Oliver Su*, “ Linear Oligoarylamines: Electrochemical, EPR, and Computational Studies of Their Oxidative States”, Journal of Physical Chemistry A, 2015, 119, 1933-1942. (SCI).  
(5)  Te-Fang Yang*, Chi-Yi Chang, Wei-Fan Lin, “Rearrangement of acyclic-alkyl [3.2.1]bicyclic alcohols to free
methylene dimethyl alkyl [2.2.2]bicyclic octanes: application to preparation of stereospecific novel sesquiterpene and terpenoids”. Tetrahedron Letters, 2015, 56, 801-804. (SCI).
(6)  Hsu-Chun Cheng; Kuo Yuan Chiu; Yi-Jung Tu; Te-Fang Yang*; Yulong Oliver Su*, “Electrochemically Controlled Multiple Hydrogen Bonding between Triarylamines and Imidazoles”.
Organic Letters, 2013, 15 3868-3871. (SCI). 
(7) Te-Fang Yang*; Kuan-Yu Wang; Hsuan-Wei Li; Yang-Chan Tseng; Tai-Chen Lien, “Synthesis of substituted alpha-tetralones and substituted 1naphthols via regioselective ring expansion of 1-acyl-1-indanol skeleton”. Tetrahedron Letters, 2012, 53, 585-588. (SCI).
(8) Te-Fang Yang*; Kuo Yuan Chiu; Hsu-Chun Cheng; Yan Wei Lee; Ming-Yu Kuo*;Yuhlong Oliver Su*, “Studies on the Structure of N-Phenyl-Substituted Hexaaza[16]paracyclophane: Synthesis, Electrochemical Properties, And Theoretical Calculation”. The Journal of Organic Chemistry, 2012, 77, 8627-8633. (SCI).      
(9) C. -Y. Huang; C. -Y. Hsu; L. -Y. Yang; C. -J. Lee; Te-Fang Yang; C. -C. Hsu; C. -H. Ke; Y. O. Su*, “A systematic Study of Electrochemical and Spectral Properties for the Electronic Interactions in Porphyrin-Triphenylamine Conjugates”, Eur. J. Inorg. Chem. 2012, 1308-1047. 
(10) Te-Fang Yang*; L.-H. Chen; L. –T. Kao; C. –H. Chuang; Y. –Y. Chen, “Condensation-ring expansion reaction of formyl [2.2.1]bicyclic carbinols with para-substituted phenyl amines: application to the preparation of [3.2.1]bicyclic N-aryl-1,2,3-oxathiazolidine- 2-oxide agents”, J. Chin. Chem. Soc. 2012, 59, 378-388. 
(11) K. Y. Chiu, Y. -J. Tu; C. -J. Lee; Te-Fang Yang*; L. -L. Lai; I. Cho*; Y. O. Su*, “Unusual Spectral and Electrochemical Properties of Azobenzene-Substituted Porphyrins”, Electrochimica Acta 2012, 62, 51-62.  
(12) Te-Fang Yang*; C. -H. Shen; C. -T. Hsu; L. -H. Chen; C. -H. Chuang, “Selective reaction of camphor-derived exo-formyl [2.2.1]bicyclic carbinol with alkyl primary amines: application to the preparation of new chiral catalysts for asymmetric reduction of aryl ketones”, Tetrahedron 2010, 66, 8734-8738. 
(13) Te-Fang Yang*; C. -H. Tseng; C. -H. Shen; L. -H. Chen; L. -T. Kao, “Regio- and stereoselective rearrangements of formyl [2.2.1]bicyclic carbinols in methanol”, Tetrahedron 2009, 65, 9854-9861. 
(14) Te-Fang Yang*; C. -H. Tseng; K. -I Wu; C. -N. Chang, “Selective Ring Expansion Alkylation    
       of Formyl[2.2.1]bicyclic Carbinols with C-Nucleophiles: A Unique Route to Cyclopentane
       Derivatives”, J. Org. Chem. 2007, 72, 7034-7037.