{"id":8,"date":"2013-04-08T15:51:20","date_gmt":"2013-04-08T07:51:20","guid":{"rendered":"http:\/\/wp.kmu.edu.tw\/clkao\/?page_id=8"},"modified":"2021-11-03T11:53:23","modified_gmt":"2021-11-03T03:53:23","slug":"%e7%a0%94%e7%a9%b6%e8%91%97%e4%bd%9c","status":"publish","type":"page","link":"https:\/\/wp.kmu.edu.tw\/clkao\/%e7%a0%94%e7%a9%b6%e8%91%97%e4%bd%9c\/","title":{"rendered":"Publications"},"content":{"rendered":"<ol>\n<li>Dorairaj, D. P.; Lin, Y.-F.; Haribabu, J.; Murugan, T.; Narwane, M.; Karvembu, R.; Neelakantan, M. A.; <strong>Kao, C.-L.<\/strong>; Chiu, C.-C.*;Hsu, S. C. N.*, \u201cBinding mode transformation and biological activity on the Ru(II)-DMSO complexes bearing heterocyclic pyrazolyl ligands\u201d Inorg. Biochem. <strong>2021<\/strong>,223, 111545.<\/li>\n<li>Huang, Yen-Chung; Chen, Hsing-Yin; Chang, Yu-Lun; Vasanthakumar, Punitharaj; Chen, Shih-Yun; <strong>Kao, Chai-Lin<\/strong>; Wu, Carol Hsin-Yi; Hsu, Sodio C. N. Synthesis of triisocyanomesitylene \u03b2\u2011diketiminato copper(I) complexes and evaluation of isocyanide \u03c0-back bonding.Polyhedron <strong>2020,<\/strong> 192, 114828<\/li>\n<li>Lyu, L. Ding, A.Y.-T. Huang, <strong>C.-L. Kao<\/strong>, L. Peng. Poly(amidoamine) dendrimers: covalent and supramolecular synthesis. Materials Today Chemistry. <strong>2019<\/strong>,13,34-48<\/li>\n<li>Ding, L.; Lyu, Z. B.; Dhumal, D.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Bernard, M.; Peng, L. Dendrimer-based magnetic resonance imaging agents for brain cancer. SCIENCE CHINA-MATERIALS.\u00a0<strong>2018<\/strong>,\u00a0<em>61(11)<\/em>,1420-1443. (invited review)<\/li>\n<li>Tang, Y.-H.; Hsu, S.C.N.; Chen, P.-Y.; Liou, S.-T.; Chen, H.-T.; Wu, C. .-Y.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>Importance of Binding Affinity for the Activity of a Metallodendritic Chemical Nuclease.\u00a0<em>Pharmaceutics<\/em>\u00a0<strong>2018<\/strong>,\u00a0<em>10<\/em>, 258.<\/li>\n<li>Lu, H.-F.; Chen, H.-F.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Chao, I.; Chen, H.-Y.* A computational study of the Fenton reaction in different pH ranges.\u00a0<em> Chem. Phys.<\/em>,\u00a0<strong>2018<\/strong>,\u00a0<em>20<\/em>, 22890-22901<\/li>\n<li>Chuang, W.-J.; Narwane, M.; Chen, H.-Y.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Huang, B.; Hsu, K.-M.; Wang, Y.-M.*; Hsu, Sodio C. N.* Nitric Oxide Release Study of a Bio-\u200binspired Copper(I)\u200b-\u200bnitrito Complex on Chemical and Biological Conditions.\u00a0<em>Dalton Trans.<\/em><strong>2018<\/strong>,\u00a0<em>47<\/em>, 13151-13157.<\/li>\n<li>Chang, Y. L.; Lin, Y. F.; Chuang, W. J.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Narwane, M.; Chen, H.-Y.; Chiang, M. Y.; Hsu, S. C. N. Structure and nitrite reduction reactivity study of bio-inspired copper(I)-nitro complexes in steric and electronic considerations of tridentate nitrogen ligands.\u00a0<em>Dalton Trans.<\/em><strong>2018<\/strong>,\u00a0<em>47<\/em>(15), 5335-534.<\/li>\n<li>Tsai, C.-H.; Tang,Y.-H.; Chen,H.-T.; Yao,Y.-W.; Chien, T.-C.*;<strong><u>Kao, C.-L.*<\/u><\/strong>\u00a0A selective glucose sensor: cooperative effect by monoboronic acid-modified poly(amidoamine) dendrimers.\u00a0\u00a0<strong>2018<\/strong>,\u00a0<strong>54<\/strong>, 4577-4580<\/li>\n<li>Selvaraj, A.; Chen, H.-T.; Huang, A. Y.-T.;\u00a0<strong><u>Kao, C.-L.*<\/u><\/strong>; Expedient on-resin modification of a peptide C-terminus through a benzotriazole linker.\u00a0,<strong>2018<\/strong>,\u00a0<em>9<\/em>, 345\u2013349<\/li>\n<li>Tang, Y.-H.; Cangiotti, M.;\u00a0<strong><u>Kao, C.-L.*<\/u><\/strong>; Ottaviani, M. F.* EPR Characterization of Copper(II) Complexes of PAMAM-Py Dendrimers for Biocatalysis in the Absence and Presence of Reducing Agents and a Spin Trap.\u00a0<em> Chem. B<\/em>,\u00a0<strong>2017<\/strong>,\u00a0<em>121<\/em>(46),\u00a0pp 10498\u201310507<\/li>\n<li>Tsai, C.-H.; Fang, Y.-W.; Chen, H.-T.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>* Accelerated hydrolysis of boronic acid in a modified poly(amidoamine) dendrimer: identification of a factor leading to the production of an impurity in boronic acid containing poly(amidoamine) dendrimers.\u00a0<em>Canadian J. Chem.<\/em>,\u00a0<strong>2017<\/strong>,\u00a0<em>95<\/em>(9), 984-990.<\/li>\n<li><strong><u>Kao, C.-L.*<\/u><\/strong>; Huang, Adela, Y.-T.; Chen, H.-T. Solid-phase synthesis of a seventh-generation inverse poly(amidoamine) dendrimer: importance of the loading ratio on the resin.\u00a0<em>Rapid Commun.\u00a0<\/em><strong>2017<\/strong>,\u00a0<em>38<\/em>(DOI: 10.1002\/marc.201700062)<\/li>\n<li>Wang, Y.-S.; Yeh, H.-W.; Tang, Y.-H.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Chen, P.-Y. Voltammetric Study and Electrodeposition of Zinc in Hydrophobic Room-\u200bTemperature Ionic Liquid 1-\u200bButyl-\u200b1-\u200bmethylpyrrolidinium Bis((trifluoromethyl)\u200bsulfonyl)\u200bimide ([BMP]\u200b[TFSI]\u200b)\u200b: A Comparison between Chloride and TFSI Salts of Zinc.\u00a0<em> Soc.<\/em><strong>2017<\/strong>,\u00a0<em>164(2)<\/em>, D39-D47.<\/li>\n<li>Ingersoll, M. A.; Miller, D. R.; Martinez, O.; Wakefield, C. B.; Hsieh, K.-C.; Simha, M. V.;\u00a0<strong>Kao, C.-L<\/strong>.; Chen, H.-T.*; Batra, S. K.; Lin, M.-F.* Statin derivatives as therapeutic agents for castration-\u200bresistant prostate cancer.\u00a0<em>Cancer Lett.<\/em><strong>2016<\/strong>,\u00a0<em>383<\/em>, 94-105.<\/li>\n<li>Chen, Y.-H.; Kirankumar, R.; Kao, C.-L.; Chen, P.-Y., Electrodeposited Ag, Au, and AuAg nanoparticles on graphene oxide-\u200bmodified screen-\u200bprinted carbon electrodes for the voltammetric determination of free sulfide in alkaline solutions.\u00a0<em>Electrochimica Acta<\/em><strong>2016<\/strong>,\u00a0<strong>205<\/strong>, 124-131.<\/li>\n<li>Huang, A. Y.-T.; Patra, S.; Chen, H.-T.;\u00a0<strong>Kao, C.-L.*<\/strong>; Simanek, E. E.* Solid-Phase Synthesis of Libraries of Triazine Dendrimers and Orthogonal Staining Methods for Tracking Reactions on Resin.\u00a0<em>Asian J. Org. Chem.\u00a0<\/em><strong>2016<\/strong>,\u00a0<em>5<\/em>, 860\u2013864<\/li>\n<li>Tseng, H.-Y.; Chen, H.-P.; Tang, Y.-H.; Chen, H.-T.;\u00a0<strong>Kao, C.-L.<\/strong>*; Wang, S.-C.* The debye light scattering equation\u2019s scaling relation reveals the purity of synthetic dendrimers.\u00a0<em>J Nanopart Res,\u00a0<\/em><strong>2016<\/strong>,<em>18, 1-8.<\/em><\/li>\n<li>Lai, Y.-S.;\u00a0<strong>Kao, C.-L.<\/strong>; Chen, Y.-P.; Fang, C.-C.; Hu, C.-C.; Chu, C.-C. Photodegradable self-\u200bassembling PAMAM dendrons for gene delivery involving dendriplex formation and phototriggered circular DNA release,\u00a0<em>New J. Chem.<\/em><strong>2016<\/strong>,\u00a0<em>40<\/em>(3), 2601-2608.<\/li>\n<li>Lo, N. C.; Tang, Y.-H.;\u00a0<strong>Kao, C. L.<\/strong>; Sun, I-W.; Chen, P. Y. Electrochemical formation of palladium nanoparticles in a salicylate-based hydrophilic ionic liquid: The effect of additives on particle morphology and electrochemical behavior.\u00a0<strong>2016<\/strong>,\u00a0<em>62<\/em>, 60\u201363.<\/li>\n<li>Chen, Y.-H.; Kirankumar, R.; Huang, A. Y. T.; Lu, C. Y.;\u00a0<strong>Kao, C.-L.<\/strong>; Chen, P. Y. Electrochemical study of a new nonheme iron complex-modified carbon ionic liquid electrode with electrocatalytic activity towards hydrogen peroxide reduction.\u00a0<em>Electrochimica Acta\u00a0<\/em><strong>2015<\/strong>,\u00a0<em>184<\/em>, 316\u2013322.<\/li>\n<li>Tang, Y.-H.; Lin, Y. C.; Hsu, S. C. N.; Liou, S.-T.; Chen, H.-Y.; Hsien, K.-C.; Chuang, W.-J.; Chiu, L.-T.; Chen, Y.-L.;\u00a0<strong>Kao, C.-L.*<\/strong>Cooperative Effects in Copper Polyamidoamine Dendrimer Complexes Catalyzing the Reduction of Molecular Oxygen.\u00a0<em> Inorg. Chem.<\/em>\u00a0<strong>2015<\/strong>, 4839\u20134847.<\/li>\n<li>Chen, H.-Y.; Yang, P.-Y.; Chen, H.-F.; Kao, C.-L.; Liao, L.-W. DFT reinvestigation of DNA strand breaks induced by electron attachment.\u00a0<em> Chem. B<\/em>,\u00a0<strong>2014<\/strong>,\u00a0<em>118<\/em>, 11137-11144.<\/li>\n<li>Hsieh, K.-C.;\u00a0<strong>Kao, C.-L.<\/strong>; Feng, C.-W.; Wen, Z.-H.; Chang, H.-F.; Chuang, S.-C.; Wang, G.-J.; Ho, M.-L.; Wu, S.-M.; Chang, J.-K.; Chen, H.-T. A Novel Anabolic Agent: A Simvastatin Analogue without HMG-\u200bCoA Reductase Inhibitory Activity.\u00a0<strong>2014<\/strong>,\u00a0<em>16<\/em>, 4376-4379<\/li>\n<li>Chen, H.-Y.; Chen, H.-F.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Yang, P.-Y.; Hsu, S. C. N. Interaction of electrons with cisplatin and the subsequent effect on DNA damage: a density functional theory study.\u00a0<em> Chem. Phy.<\/em><strong>2014<\/strong>,\u00a0<em>16<\/em>, 19290-19297.<\/li>\n<li>Hsu, S. C. N.; Wang, T.-P.\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Chen, H.-F.; Yang, P.-Y.; Chen, H.-Y.\u00a0Theoretical Study of the Protonation of the One-Electron-Reduced Guanine\u2212Cytosine Base Pair by Water.\u00a0<em> Chem. B<\/em>,<strong>2013<\/strong>,\u00a0<em>117<\/em>, 2096\u22122105.<\/li>\n<li>Patra, S.; Kozura, B.; Huang, A. Y.-T.; Enciso, A. E.; Sun, X.; Hsieh, J.-T.;\u00a0<strong><u>Kao, C.-L.;\u00a0<\/u><\/strong>Chen, H.-T.; Simanek, E. E. Dendrimers terminated with dichlorotriazine groups provide a route to compositional diversity.\u00a0<em>Organic Letters<\/em>,\u00a0<strong>2013<\/strong>,\u00a0<em>15<\/em>, 3808\u20133811.<\/li>\n<li>Huang, A, Y.-T.; Tsai, C.-H.; Chen, H.-Y.; Chen, H.-T.; Lu, C.-Y.; Lin, Y.-T.;<strong><u>Kao, C.-L.<\/u>*<\/strong>\u00a0Concise solid-phase synthesis of inverse poly(amidoamine) dendrimer dendrons using AB<sub>2<\/sub>\u00a0building blocks.\u00a0<em>Commun<\/em>.<strong>\u00a02013<\/strong>,\u00a0<em>49<\/em>, 5784-5786.<\/li>\n<li>Chen, Y.-H.; Lin, T. T.Y.; Chen, H.-Y.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Chen, H.-Y.; Hsu, S. C.N.*; Carey, J. R.*; Chiang, M. Y.* A simple competition assay to probe pentacopper(I)-thiolato cluster ligand exchange.\u00a0<em> Biochem.<\/em>,\u00a0<strong>2013<\/strong>,\u00a0<em>120<\/em>. 24-31.<\/li>\n<li>Hsu, Sodio C. N. *; Chang, Y.-L.; Chuang, W.-J.; Chen, H.-Y.; Lin, I.-J.; Chiang, Michael Y.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Chen, H.-Y. Copper(I) Nitro complex with an anionic [HB(3,5-Me2Pz)3]- ligand: A synthetic model for the copper nitrite reductase active site.\u00a0<strong>2012<\/strong>,\u00a0<em>51<\/em>, 9297-9308.<\/li>\n<li>Su, C.-J.; Tang, Y.-H.; Yu, F.-L.; Wu, R.-R.; Hsu, Sodio C. N. *;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>*; Huang, H.-Y.; Chen, P.-Y.* Extraction of cupric ions with ionic liquids containing polypyridine-type small molecules or peripherally pyridine-modified dendrimers.\u00a0<em>Chemistry\u2013An Asian J.<\/em><strong>2012<\/strong>,\u00a0<em>7<\/em>, 2438-2445.<\/li>\n<li>Lee, C.-Y.; Chen, Y.-C. Lin, H.-C. Jhong, Y. Chang, C.-W. Tsai, C.-H.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>* Chien, T.-C.* Facile synthesis of 4-arylidene-5-imidazolinones as synthetic analogs of fluorescent protein chromophore.\u00a0<em>Tetrahedron<\/em>,\u00a0<strong>2012<\/strong>,\u00a0<em>68<\/em>, 5898-5907.<\/li>\n<li>Tang, Y.-Y.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Chen, P.-Y.* Electrochemical detection of hydrazine using a highly sensitive nanoporous gold electrode.\u00a0<em> Acta<\/em>,\u00a0<strong>2012<\/strong>,\u00a0<em>711<\/em>, 32-39.<\/li>\n<li>Tseng, C.-H.; Tzeng, C.-C.; Chung, K.-Y.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Hsu, C.-Y.; Cheng, C.-M.; Huang, K.-S.; Chen, Y.-L.* Synthesis and antiproliferative evaluation of 6-aryl-11-iminoindeno[1,2-c]quinoline derivatives.\u00a0<em> Chem.<\/em><strong>2011<\/strong>,\u00a0<em>19<\/em>, 7653-7663.<\/li>\n<li>Chen, Po.-Y.; Wang, T.-P.; Huang, K.-S.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Tsai, J.-C.; Wang, E.-C. * tert-BuOK-mediated carbanion-yne intramolecular cyclization: synthesis of 2-substituted 3-benzylbenzofurans.\u00a0<em>Tetrahedron\u00a0<\/em><strong>2011<\/strong>,\u00a0<em>67<\/em>, 9291-9297.<\/li>\n<li>Tang, Y.-H.; Huang, Adela Y.-T.; Chen, P.-Y. Chen, H.-T.*;<strong><u>Kao, C.-L.<\/u><\/strong>\u00a0* Metallodendrimers and Dendrimer Nanocomposites.\u00a0<em>Current Pharmaceutical Design<\/em>,\u00a0<strong>2011<\/strong>,\u00a0<em>17<\/em>, 2308-2330.<\/li>\n<li><strong><u>Kao, C.-L.*<\/u><\/strong>, Tang, Y.-h.; Lin,Y. C.; Chiu, L.-T.; Chen, H.-T.; Hsu, Sodio C.N.; Hsieh, K.-C.; Lu, C.-Y.; Chen, Y.-L. Copper complex of a pyridine-modified poly(amidoamine) dendrimer as a chemical nuclease: Synthetic and catalytic study.\u00a0<em>Nanomedicine: Nanotechnology, Biology and Medicine.<\/em><strong>2011<\/strong>,\u00a0<em>7<\/em>, 273-276.<\/li>\n<li>Lo, W.-S.; Hu, W.-P.; Lo, H.-P.; Chen, C.-Y.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Vandavasi, J. K.; Wang, J.-J.* Synthesis of sulfur-sulfur bond formation from thioamides promoted by 2,3-dichloro-5,6-dicyanobenzoquinone\u00a0<em>Organic Letters<\/em>,\u00a0<strong>2010<\/strong>,\u00a0<em>12<\/em>, 5570-5572.<\/li>\n<li>Kasala, D.; Lin, T.-S.; Chen, C.-Y. Liu, G.-C.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Cheng, T.-L.; Wang, Y.-M.* [Gd(Try-TTDA)(H2O)]<sup>2-<\/sup>: A new MRI contrast agent for copper ion sensing.\u00a0<em>Dalton Trans.<\/em>,\u00a0<strong>2011<\/strong>,\u00a0<em>40<\/em>, 5018-5025.<\/li>\n<li>Chen, H-Y*; Yeh, S-W; Hsu, Sodio C. N.;\u00a0<strong><u>Kao, C-L.<\/u><\/strong>; Dong, T.-Y. Effect of nucleobase sequence on the proton-transfer reaction and stability of the guanine\u2013cytosine base pair radical anion.\u00a0<em> Chem. Phys.<\/em>,\u00a0<strong>2011<\/strong>, 13, 2674\u20132681.<\/li>\n<li>Huang, H.-Y.; Su, C.-J.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Ch., P.-Y.* Electrochemical study of Pt and Fe and electrodeposition of PtFe alloys from air- and water-stable room temperature ionic liquids.\u00a0<em> Chem.<\/em><strong>2010<\/strong>,<em>650<\/em>,\u00a01-9.<\/li>\n<li>Tang, Y.-H.; Lin, Y.-C.; Lin, Y.-S.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>* Metallodendrimer as catalyst in organic reactions. Huaxue,\u00a0<strong>2010<\/strong>,\u00a0<em>68<\/em>, 105-117.<\/li>\n<li>Chen, H.-Y.<sup>*<\/sup>; Hsu, Sodio C. N.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>Microhydration of 9-methylguanine:1-methylcytosine base pair and its radical anion: a density functional theory study.\u00a0<em> Chem. Phy.<\/em>\u00a0<strong>2010<\/strong>,\u00a0<em>12<\/em>, 1253-1263.<\/li>\n<li>Yang, C.-L.; Tseng, C.-H.; Chen, Y.-L.; Lu, C.-M.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Wu, M.-H.; Tzeng, C.-C.* Identification of benzofuro[2,3-b]quinoline derivatives as a new class of antituberculosis agents.\u00a0<em> of Med. Chem.\u00a0<\/em><strong>2010<\/strong>,\u00a0<em>45<\/em>, 602-607.<\/li>\n<li>Chen, H.-Y.*;\u00a0<strong><u>-L.<\/u><\/strong>; Hsu, S. C. N. Proton Transfer in Guanine-Cytosine Radical Anion Embedded in B-Form DNA.\u00a0<em>J. Am. Chem. Soc.<\/em><strong>2009<\/strong>,\u00a0<em>131<\/em>, 15930\u201315938.<\/li>\n<li>Hsien, K.-C.; Chen, H.-T.; Chen, Y.-C.; Chen, Y.-L.; Lu, C.-Y.;\u00a0<strong><u>-L.*<\/u><\/strong>Pyridoxal 5\u2032-Phosphate Binding in Lysine-Modified PAMAM Dendrimers: A Biomimetic Approach.\u00a0<em>Org. Lett<\/em>.\u00a0<strong>2009<\/strong>,\u00a0<em>11<\/em>, 3526-3529.<\/li>\n<li>Chen, Y.-L.; Chen, Y.-W.; Lo, W.-F.;\u00a0<strong><u>Kao, C. L.<\/u><\/strong>; Liu, Y.-S.; Yao, C.-W.; Tzeng, C.-C. Synthesis and antimycobacterial evaluation on arylsulfonyl and arylcarbonyl derivatives of ofloxacin.\u00a0<em> Chem. Soc.<\/em><strong>2009<\/strong>,\u00a0<em>56<\/em>, 374-380.<\/li>\n<li>Huang, Y.-L.; Cheng, Y.-H.; Hsien, K.-C.; Chen, Y.-L.;\u00a0<strong><u> L.<\/u><\/strong><u>*<\/u>Concise bromodecarboxylation of cinnamic acids to \u03b2-bromostyrenes.\u00a0<em>Tetrahedron Lett.<\/em>\u00a0<strong>2009<\/strong>,\u00a0<em>50<\/em>, 1834-1837.<\/li>\n<li>Hu, W.-P.; Liang, J.-J.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Chen, Y.-C.; Chen, C.-Y.; Tsai, F.-Y.; Wu, M.-J.; Chang, L.-S.; Chen, Y.-L.; Wang, J.-J.* Synthesis and antitumor activity of novel enediyne-linked pyrrolo[2,1-c][1,4]benzodiazepine hybrids.\u00a0<em> Chem<\/em>.\u00a0<strong>2009<\/strong>,\u00a0<em>17<\/em>, 1172-1180.<\/li>\n<li><strong><u>Kao, C.-L.<\/u><\/strong>; Svetlana, S. A.; Kim, H. J.; Liu, H.-w.* Linear Aglycones Are the Substrates for Glycosyltransferase DesVII in Methymycin Biosynthesis: Analysis and Implications.\u00a0<em> Chem. Soc.\u00a0<\/em><strong>2006<\/strong>,\u00a0<em>128<\/em>, 5606-5607.<\/li>\n<li><strong><u>Kao, C.-L.<\/u><\/strong>; Kittleman, W.; Zhang, H.; Liu, H.-w.* Stereochemical Analysis of Isopentenyl Diphosphate Isomerase Type II from\u00a0<em>Staphylococcus aureus<\/em>Using Chemically Synthesized (S)- and (R)-[2-2H]Isopentenyl Diphosphates.\u00a0\u00a0<strong>2005<\/strong>,\u00a0<em>7<\/em>, 5677-5680.<\/li>\n<li>Karthikeyan, S.; Zhou, Q.; Zhao, Z.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Tao, Z.; Robinson, H.; Liu, H.-w.*; Zhang, H.* Structural Analysis of\u00a0<em>Pseudomonas\u00a0<\/em>1-Aminocyclopropane-1-carboxylate Deaminase Complexes: Insight into The Mechanism of A Unique Pyridoxal-5\u2032-Phosphate Dependent Cyclopropane Ring-Opening Reaction.\u00a0<em>Biochemistry\u00a0<\/em><strong>2004<\/strong>,\u00a0<em>43<\/em>, 13328-13339.<\/li>\n<li>Karthikeyan, S.; Zhao, Z. B.;\u00a0<strong><u>Kao, C.-L<\/u><\/strong>.; Zhou, Q. X.; Tao, Z. H.; Zhang, H; Liu, H.-w.* Structural Analysis of 1-Aminocyclopropane-L-carboxylate Deaminase: Observation of An Aminyl Intermediate and Identification of Tyr294 as The Active-Site Nucleophile.\u00a0<em> Intl. Ed. Eng.\u00a0<\/em><strong>2004<\/strong>,\u00a0<em>43<\/em>, 3425-3429.<\/li>\n<li>Borisova, S. A.; Zhao, L. S.; Melancon, C. E.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Liu, H.-w.* Characterization of The Glycosyltransferase Activity of DesVII: Analysis of and Implications for The Biosynthesis of Macrolide Antibiotics.\u00a0<em> Chem. Soc.\u00a0<\/em><strong>2004<\/strong>,\u00a0<em>126<\/em>, 6534-6535.<\/li>\n<li>Chen, C.-S.; Lai, S.-Y.; Hsu, P.-S.; Tsai, C.-Y.; Fang, C.-W.; Su, M.-J.; Cheng, F.-C.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Chern, J.-W.* Design, Synthesis and Biological Evaluation of Heterocycle-Conjugated Styrene Derivatives as Protein Tyrosine Kinase Inhibitors and Free Radical Scavengers.<em> J.\u00a0<\/em><strong>2002<\/strong>,\u00a0<em>54<\/em>, 353-374.<\/li>\n<li><strong><u>Kao, C.-L.<\/u><\/strong>; Yen, S. Y.; Chen, G. S.; Chern, S.-S.; Chern, J.-W.* Intramolecular Friedel-Crafts Acylation\u00a0<em>versus\u00a0<\/em>Intramolecular Transacetalization \u2015 A Novel Approach towards the Synthesis of Substituted Naphthalene Derivatives.\u00a0<em> J.\u00a0<\/em><strong>2002<\/strong>,\u00a0<em>54<\/em>, 375-391.<\/li>\n<li><strong><u>Kao, C.-L.<\/u><\/strong>; Chern, J.-W.* A Novel Strategy for The Synthesis of Benzofuran Skeleton Neolignans: Application to Ailanthoidol, XH-14, and Obovaten.\u00a0<em> Chem.\u00a0<\/em><strong>2002<\/strong>,\u00a0<em>67<\/em>, 6772-6787.<\/li>\n<li><strong><u>Kao, C.-L.<\/u><\/strong>; Chern, J.-W.* A Conventient Synthesis of Naturally Occurring Benzofuran Ailanthoidol.\u00a0<em>Tetrahedron Lett.<\/em><strong>2001<\/strong>,\u00a0<em>42<\/em>, 1111-1113.<\/li>\n<li><strong><u>Kao, C.-L.<\/u><\/strong>; Yen, S. Y.; Chern, J.-W.* A new route towards the synthesis of substituted naphthalenes via Friedel-Crafts acylation.\u00a0<em>Tetrahedron Lett.<\/em><strong>2000<\/strong>,\u00a0<em>41<\/em>, 2207-2210.<\/li>\n<li>Chern, J.-W.*; Lin, H.-M.; Cheng, F.-C.; Lo, J.-C.; Lai, N.-Y.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Usifoh, Cyril O. Studies on 1,2,4-benzothiadiazine 1,1-dioxide, IX. Synthesis and pharmacological evaluation of 1,2,4-benzothiadiazine 1,1-dioxide biphenyl tetrazoles as angiotensin II antagonists.\u00a0<em>Journal of the Chinese Chemical Society (Taipei)<\/em>,\u00a0<strong>1998<\/strong>,\u00a0<em>45<\/em>, 805-810.<\/li>\n<li>Tsai, Y.-M.*; Chang, F.-C.; Huang, J.; Shiu, C.-L.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Liu, J.-S. Generation and intramolecular cyclization of a-phenylsulfenyl and a-alkylsulfenyl radicals.\u00a0<em>Tetrahedron<\/em><strong>1997<\/strong>,\u00a0<em>53<\/em>, 4291-4308.<\/li>\n<li>Chen, S.-T.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Wang, K.-T.* Alkaline protease catalysis of a secondary amine to form a peptide bond.\u00a0<em>International Journal of Peptide &amp; Protein Research,<\/em><strong>1995<\/strong>,\u00a0<em>46<\/em>, 314-319.<\/li>\n<li>Chen, S.-T.; Chen, S.-Y.;\u00a0<strong><u>Kao, C.-L.<\/u><\/strong>; Wang, K.-T.* Improved yield by cryoeffect in kinetically controlled peptide synthesis catalyzed with alcalase.\u00a0<em>Letters<\/em>,\u00a0<strong>1994<\/strong>,\u00a0<em>16<\/em>, 1075-1080.<\/li>\n<li>Chen, S.-T.; Chen, S.-Y.; <strong><u>Kao, C.-L.<\/u><\/strong>; Wang, K.-T.* Proline as nucleophile in kinetically controlled peptide synthesis catalyzed by alcalase in 2-methyl-2-propanol.\u00a0<em>Med. Chem. Lett.<\/em>,\u00a0<strong>1994<\/strong>,\u00a0<em>4<\/em>, 443-448.<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>Dorairaj, D. P.; Lin, Y.-F.; Haribabu, J &hellip; <a href=\"https:\/\/wp.kmu.edu.tw\/clkao\/%e7%a0%94%e7%a9%b6%e8%91%97%e4%bd%9c\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":27,"featured_media":0,"parent":0,"menu_order":1,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_exactmetrics_skip_tracking":false,"_exactmetrics_sitenote_active":false,"_exactmetrics_sitenote_note":"","_exactmetrics_sitenote_category":0,"footnotes":""},"class_list":["post-8","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/wp.kmu.edu.tw\/clkao\/wp-json\/wp\/v2\/pages\/8","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/wp.kmu.edu.tw\/clkao\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/wp.kmu.edu.tw\/clkao\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/wp.kmu.edu.tw\/clkao\/wp-json\/wp\/v2\/users\/27"}],"replies":[{"embeddable":true,"href":"https:\/\/wp.kmu.edu.tw\/clkao\/wp-json\/wp\/v2\/comments?post=8"}],"version-history":[{"count":8,"href":"https:\/\/wp.kmu.edu.tw\/clkao\/wp-json\/wp\/v2\/pages\/8\/revisions"}],"predecessor-version":[{"id":143,"href":"https:\/\/wp.kmu.edu.tw\/clkao\/wp-json\/wp\/v2\/pages\/8\/revisions\/143"}],"wp:attachment":[{"href":"https:\/\/wp.kmu.edu.tw\/clkao\/wp-json\/wp\/v2\/media?parent=8"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}