{"id":3772,"date":"2024-05-01T14:52:47","date_gmt":"2024-05-01T06:52:47","guid":{"rendered":"\/chemistry\/?p=3772"},"modified":"2025-12-19T23:34:21","modified_gmt":"2025-12-19T15:34:21","slug":"%e8%ac%9d%e4%bb%81%e5%82%91","status":"publish","type":"post","link":"\/chemistry\/?p=3772","title":{"rendered":"\u8b1d\u4ec1\u5091(\u671f\u520a)"},"content":{"rendered":"\n<div class=\"wp-block-tkuwpbs5-bs5-container container chem_teach\" style=\"margin-top:var(--wp--preset--spacing--40);padding-top:var(--wp--preset--spacing--50);padding-bottom:var(--wp--preset--spacing--50);position:relative\" block_id=\"lq3fs6oyzthhmnpj8a\"><style><\/style>\n<div class=\"wp-block-tkuwpbs5-bs5-row row\">\n<h4 class=\"wp-block-heading\"><strong>International Award:<\/strong><\/h4>\n\n\n\n<p>2015 Asian Core Program Lectureship Award (Japan)<\/p>\n\n\n\n<p>2015 Asian Core Program Lectureship Award (Singapore)<\/p>\n\n\n\n<p>JSPS (Japan Society for the Promotion of Science) researcher fellowship<\/p>\n\n\n\n<p>FWF (F\u00f6rderung der wissenschaftlichen Forschung) fellowship<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-tkuwpbs5-bs5-row row\"><\/div>\n\n\n\n<h6><strong>Publication list:<\/strong><\/h6>\n<ol>\n<li>Aman, H.; Huang, B.-S.; Liao, J.-Y.; Thorat, V. H.; Liao, Z.-Y.; Liu, Y.-H.; Yen, L.-T.; <strong><u>Hsieh, J.-C.<\/u><\/strong>;* Chuang, G. J.* <em>Chem. Asian J. <\/em><strong>2025<\/strong>, <em>20<\/em>, e00969. \u201cMetal Free Synthesis of Seven-Membered Biaryl Sultams\u201d<\/li>\n<li>Thorat, V. H.; Chuang, Y.-C.; Hsieh, C.-H.;* <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Adv. Synth. Catal.<\/em> <strong>2025<\/strong>, <em>367<\/em>, e202500231. \u201cNickel-Catalyzed Transannulation Reaction of 1,2,3,4-Benzothiatriazin-1,1(2H)-dioxide with Alkyne and the Detailed Investigation of Reaction Mechanism\u201d<\/li>\n<li>Thorat, V. H.; Chao, H.-Y.; Yang, P.-H.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Eur. J. Org. Chem.<\/em> <strong>2025<\/strong>, <em>28<\/em>, e202401194. \u201cScandium-Catalyzed Fischer Indole Synthesis: A Highly Efficient Construction of Complicated Indoles\u201d<\/li>\n<li>Thorat, V. H.; Huang, Y.-R.; Chao, H.-Y.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Adv. Synth. Catal.<\/em> <strong>2024<\/strong>, <em>366<\/em>, 2130\u22122135. \u201cNickel-Catalyzed Intramolecular Dual Annulation Reaction of Alkyl Nitrile-Containing 1,2,3-Benzotriazin-4(3H)-ones: A Pathway to Access Diversely Polycyclic Quinazolinone Alkaloids\u201d<\/li>\n<li>Cheng, Y.-Y.; Kuo, T.-S.; Wu, P.-Y.; <strong><u>Hsieh, J.-C.<\/u><\/strong>;* Wu, H.-L.* <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, <em>89<\/em>, 4861\u22124876. \u201cRhodium(I)\/Chiral Diene Complexes Catalyzed Asymmetric Desymmetrization of Alkynyl-Tethered 2,5-Cyclohexadienones Through an Arylative Cyclization Cascade\u201d<\/li>\n<li>Thorat, V. H.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Org. Lett.<\/em> <strong>2023<\/strong>, <em>25<\/em>, 7990\u20137994. \u201cNickel-Catalyzed Intramolecular Dual Annulation Reaction of Aryl Nitrile-Containing 1,2,3-Benzotriazin-4(3H)-ones: A Pathway to Synthesize Luotonin A and Related Polycyclic Pyrroloquinazolinones\u201d<\/li>\n<li>Thorat, V. H.; Tsai, Y.-L.; Huang, Y.-R.; Cheng, C.-H.;* <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Org. Lett.<\/em> <strong>2022<\/strong>, <em>24<\/em>, 2915\u20132920. \u201cNickel-Catalyzed Denitrogenative Cyclization of 1,2,3,4-Benzothiatriazin-1,1(2H)-dioxides with Arynes to Synthesize Biaryl Sultams\u201d<\/li>\n<li>Aman, H.; Huang, Y.-C.; Liu, Y.-H.; Tsai, Y.-L.; Kim, M.; <strong><u>Hsieh, J.-C.<\/u><\/strong>;* Chuang, G. J.* <em>Molecules<\/em> <strong>2021<\/strong>, <em>26<\/em>, 7212. \u201cCobalt-Catalyzed Cyclization of 2-Bromobenzamides with Carbodiimides: A New Route for the Synthesis of 3-(Imino)isoindolin-1-ones\u201d<\/li>\n<li>Thorat, V. H.; Aman, H.; Tsai, Y.-L.; Pallikonda, G.; Chuang, G. J.;* <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Org. Chem. Front.<\/em> <strong>2021<\/strong>, <em>8<\/em>, 6419\u20136426. \u201cCobalt-Catalyzed Coupling Reactions of 2-Halobenzamides with Alkynes: Investigation of the Ligand-Controlled Dual Pathways\u201d<\/li>\n<li><strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Chem. Rec.<\/em> <strong>2021<\/strong>, <em>21<\/em>, 3370\u20133381. \u201cTransition-Metal-Catalyzed Addition\/Cyclization Reactions of the C-N Multiple Bonds Containing Species\u201d<\/li>\n<li>Wang, H.-K.; Ciou, Y.-L.; Pallikonda, G.; Wu, H.-L.;* Su, H.-L.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Molecules<\/em> <strong>2020<\/strong>, <em>25<\/em>, 5303. \u201cCopper-Catalyzed Dual Cyclization for the Synthesis of Quinindolines\u201d (Invited paper for special issue)<\/li>\n<li>Thorat, V. H.; <strong><u>Hsieh, J.-C.<\/u><\/strong>;* Cheng, C.-H.* <em>Org. Lett.<\/em> <strong>2020<\/strong>, <em>22<\/em>, 6623\u20136627. \u201cTransition-Metal-Free Tandem Cyclization\/N-Arylation Reaction: A Method to Access Biaryl Sultam Derivatives via a Diradical Pathway\u201d<\/li>\n<li><strong><u>Hsieh, J.-C.<\/u><\/strong>;* Su, H.-L.<em> Synthesis<\/em> <strong>2020<\/strong>, <em>52<\/em>, 819\u2013833. \u201cSynthesis of N-Heterocycles via the Transition-Metal-Catalyzed Tandem Addition\/Cyclization of a Nitrile\u201d (Invited short review)<\/li>\n<li>Pallikonda, G.; Hsieh, C.-Y.; Su, H.-L.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Res. Chem. Intermed.<\/em> <strong>2019<\/strong>, <em>45<\/em>, 5399\u20135407. \u201cA Combined Pathway for the Synthesis of Nitidine Family Alkaloids\u201d (Invited paper for special issue)<\/li>\n<li>Yeh, L.-H.; Wang, H.-K.; Pallikonda, G.; Ciou, Y.-L.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Synfacts<\/em>, <strong>2019<\/strong>, <em>15<\/em>, 513. \u201cPalladium-Catalyzed Dual Annulation: Towards the Norneocryptolepine Core\u201d<\/li>\n<li>Yeh, L.-H.; Wang, H.-K.; Pallikonda, G.; Ciou, Y.-L.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Org. Lett.<\/em> <strong>2019<\/strong>, <em>21<\/em>, 1730\u20131734. \u201cPalladium-Catalyzed Dual Annulation: A Method for the Synthesis of Norneocryptolepine\u201d<\/li>\n<li>Chen, M.-H.; <strong><u>Hsieh, J.-C.<\/u><\/strong>;* Lee, Y.-H.; Cheng, C.-H.* <em>ACS Catal.<\/em> <strong>2018<\/strong>, <em>8<\/em>, 9364\u20139369. \u201cControlled Synthesis of Enantioselective 1-Aminoindenes via Cobalt-Catalyzed [3+2] Annulation Reaction\u201d<\/li>\n<li><strong><u>Hsieh, J.-C.<\/u><\/strong>;* Chu, Y.-H.; Muralirajan, K.; C.-M.; Cheng, C.-H.* <em>Chem. Commun.<\/em> <em>2017<\/em>, <em>53<\/em>, 11584\u201311587. \u201cA Simple Route to 1,4-Addition Reactions by Co-Catalyzed Reductive Coupling of Organic Tosylates and Triflates with Activated Alkenes\u201d<\/li>\n<li><strong><u>Hsieh, J.-C.<\/u><\/strong>;* Hong, Y.-C.; Yang, C.-M.; Cheng, C.-H.* <em>Org. Chem. Front.<\/em> <strong>2017<\/strong>, <em>4<\/em>, 1615\u20131619. \u201cNickel Catalyzed Highly Chemo- and Stereoselectively Borylative Cyclization of 1,6-Enynes with Bis(pinacolato)diboron\u201d<\/li>\n<li>Chen, W.-L.; Jhang, Y.-Y.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Res. Chem. Intermed.<\/em> <strong>2017<\/strong>, <em>43<\/em>, 3517\u20133526. (Invited paper for special issue) \u201cCopper-Catalyzed Intramolecular C-N Coupling Reaction of Aryl Halide with Amide\u201d<\/li>\n<li>Fan-Chiang, T.-T.; Wang, H.-K.; <strong><u>Hsieh, J.-C.<\/u><\/strong>*<em> Tetrahedron<\/em> <strong>2016<\/strong>, <em>72<\/em>, 5640\u20135645. \u201cSynthesis of Phenanthridine Skeletal Amaryllidaceae Alkaloids\u201d<\/li>\n<li>Jhang, Y.-Y.; Fan-Chiang, T.-T.; Huang, J.-M.; <strong><u>Hsieh, J.-C.<\/u><\/strong>*<em> Org. Lett.<\/em> <strong>2016<\/strong>, <em>18<\/em>, 1154\u20131157. \u201cCopper-Catalyzed Annulation: A Method for the Systematic Synthesis of Phenanthridinium Bromide\u201d<\/li>\n<li>Gopula, B.; Yang, S.-H.; Kuo, T.-S.; <strong><u>Hsieh, J.-C.<\/u><\/strong>;* Wu, P.-Y.; Henschke, J. P.;* Wu, H.-L.* <em>Chem. Eur. J.<\/em> <strong>2015<\/strong>, <em>21<\/em>, 11050\u201311055. \u201cDirect Synthesis of Chiral 3-Arylsuccinimides by Rhodium-Catalyzed Enantioselective Conjugate Addition of Arylboronic Acids to Maleimides\u201d<\/li>\n<li>Liu, C.-C.; <strong><u>Hsieh, J.-C.<\/u><\/strong>;* Korivi, R.-P.; Cheng, C.-H.* <em>Chem. Eur. J.<\/em> <strong>2015<\/strong>, <em>21<\/em>, 9544\u20139549. \u201cCobalt-Catalyzed Dual Annulation of o-Halobenzaldimine with Alkyne: A Powerful Route toward Bioactive Indenoisoquinolinones\u201d<\/li>\n<li>Chen, W.-L.; Chen, C.-Y.; Chen, Y.-F.; <strong><u>Hsieh, J.-C.<\/u><\/strong>*<em> Org. Lett.<\/em> <strong>2015<\/strong>,<em> 17<\/em>, 1613\u20131616. \u201cHydride-Induced Anionic Cyclization: An Efficient Method for the Synthesis of 6-H-Phenanthridines via a Transition-Metal-Free Process\u201d<\/li>\n<li>Chen, Y.-F.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Synfacts<\/em>, <strong>2014<\/strong>, <em>10<\/em>, 1194. \u201cSynthesis of Polysubstituted Phenanthridines\u201d<\/li>\n<li>Chen, Y.-F.; <strong><u>Hsieh, J.-C.<\/u><\/strong>*<em> Org. Lett.<\/em> <strong>2014<\/strong>, <em>16<\/em>, 4642\u20134645. \u201cSynthesis of Polysubstituted Phenanthridines via Ligand-Free Copper-Catalyzed Annulation\u201d<\/li>\n<li>Chen, Y.-F.; Wu, Y.-S.; Jhan, Y.-H.; <strong><u>Hsieh, J.-C.<\/u><\/strong>*<em> Org. Chem. Front.<\/em> <strong>2014<\/strong>, <em>1<\/em>, 253\u2013257. (Invited paper) \u201cAn Efficient Synthesis of (NH)-Phenanthridinones via Ligand-Free Copper-Catalyzed Annulation\u201d<\/li>\n<li>Wan, J.-C.; Huang, J.-M.; Jhan, Y.-H.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Synfacts<\/em>, <strong>2013<\/strong>, <em>9<\/em>, 948. \u201cNitrile-Directed Palladium-Catalyzed Syntheses of Fluorenones\u201d<\/li>\n<li>Wan, J.-C.; Huang, J.-M.; Jhan, Y.-H.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Org. Lett.<\/em> <strong>2013<\/strong>, <em>15<\/em>, 2742\u20132745. \u201cNovel Syntheses of Fluorenones via Nitrile Directed Palladium-Catalyzed C\u00adH and Dual C\u00adH Bond Activation\u201d<\/li>\n<li>Jhan, Y.-H.; Kang, T.-W.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Tetrahedron Lett.<\/em> <strong>2013<\/strong>, <em>54<\/em>, 1155\u20131159. \u201cEfficient copper-catalyzed intramolecular N-arylation for the synthesis of oxindoles\u201d<\/li>\n<li><strong><u>Hsieh, J.-C.<\/u><\/strong>;* Cheng, A.-Y.; Fu, J.-H.; Kang, T.-W. <em>Org. Biomol. Chem.<\/em> <strong>2012<\/strong>, <em>10<\/em>, 6404\u20136409. \u201cCopper-Catalyzed Domino Coupling Reaction: An Efficient Method to Synthesize Oxindoles\u201d<\/li>\n<li><strong><u>Hsieh, J.-C.<\/u><\/strong>;* Chen, Y.-C.; Cheng, A.-Y.; Tseng, H.-C.<em> Org. Lett<\/em>. <strong>2012<\/strong>, <em>14<\/em>, 1282\u20131285. \u201cNickel-Catalyzed Intermolecular Insertion of Aryl Iodides to Nitriles: A Novel Method to Synthesize Arylketones\u201d<\/li>\n<li>Lee, Y.-H.; Chen, Y.-C.; <strong><u>Hsieh, J.-C.<\/u><\/strong>*<em> Eur. J. Org. Chem.<\/em><strong> 2012<\/strong>, 247\u2013250. \u201cPyridine-Catalyzed Double C\u2013N Coupling Reaction of an Isocyanate with two Benzynes\u201d<\/li>\n<li>Cheng, A.-Y.; <strong><u>Hsieh, J.-C.<\/u><\/strong>* <em>Tetrahedron Lett.<\/em> <strong>2012<\/strong>, <em>53<\/em>, 71\u201375. \u201cHighly Efficient Copper Catalytic System for the O-Arylation of Phenol with Iodoarene\u201d<\/li>\n<li>Lackner-Warton, W.; Tanaka, S.; Standfest-Hauser, C. M.; \u00d6ztopcu, \u00d6.; <strong><u>Hsieh, J.-C.<\/u><\/strong>; Mereiter, K.; Kirchner, K.* <em>Polyhedron<\/em>, <strong>2010<\/strong>, <em>29<\/em>, 3097\u20133102. &#8220;Synthesis and characterization of ruthenium p-cymene complexes bearing bidentate P\u2013N and E\u2013N ligands (E = S, Se) based on 2-aminopyridine&#8221;<\/li>\n<li><strong><u>Hsieh, J.-C.<\/u><\/strong>; Ebata, S.; Nakao, Y.;* Hiyama, T.* <em>Synlett<\/em>, <strong>2010<\/strong>, 1709\u20131711. (Invited paper) \u201cAsymmetric Synthesis of Indolines Bearing Benzylic Quaternary Carbon Center through Intramolecular Arylcyanation of Alkenes\u201d<\/li>\n<li>Lu, J.; Ma, Z.; <strong><u>Hsieh, J.-C.<\/u><\/strong>.; Fan, C.-W.; Chen, B.; Longgood, J. C.; Williams, N. S.; Amatruda, J. F.; Lum, L.; Chen, C.* <em>Bioorg. Med. Chem. Lett.<\/em> <strong>2009<\/strong>,<em> 19<\/em>, 3825\u20133827. \u201cStructure\u2013activity relationship studies of small-molecule inhibitors of Wnt response\u201d<\/li>\n<li><strong><u>Hsieh, J.-C.<\/u><\/strong>; Cheng, C.-H.* <em>Chem. Commun.<\/em> <strong>2008<\/strong>, 2992\u20132994. \u201cO-Dihaloarenes as aryne precursors for nickel-catalyzed [2+2+2] cycloaddition with alkyne and nitriles\u201d<\/li>\n<li><strong><u>Hsieh, J.-C.<\/u><\/strong>; Cheng, C.-H.* <em>Chem. Commun. 2005<\/em>, 4554\u20134556. \u201cNickel-catalyzed coupling of isocyanates with 1,3-iodoesters and halobenzenes: a novel method for the synthesis of imide and amide derivatives\u201d<\/li>\n<li><strong><u>Hsieh, J.-C.<\/u><\/strong>; Cheng, C.-H.* <em>Chem. Commun.<\/em> <strong>2005<\/strong>, 2459\u20132461. \u201cNickel-catalyzed cocyclotrimerization of arynes with diynes; a novel method for synthesis of naphthalene derivatives\u201d<\/li>\n<li><strong><u>Hsieh, J.-C.<\/u><\/strong>; Rayabarapu, D. K.; Cheng, C.-H.* <em>Chem. Commun<\/em>. <em>2004<\/em>, 532\u2013533. \u201cNickel-catalyzed highly chemoselective cocyclotrimerization of arynes with allenes: a novel method for 10-methylene-9,10-dihydrophenanthrenes\u201d<\/li>\n<li>Ma, C.C. M.;* Kuan, H.-C.; <strong><u>Hsieh, J.-C.<\/u><\/strong>.; Chiang, C.-L. <em>J. Mate. Sci.<\/em> <strong>2003<\/strong>, <em>38<\/em>, 3933\u20133944. \u201cEffects of chain extender and hard\/soft segment content on the surface and electrical properties of PDMS based polyurea-urethane\u201d<strong><br \/><\/strong><\/li>\n<\/ol>\n<p><!--more--><\/p>\n<\/div>\n\n\n\n<div style=\"height:10px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Publication list: Aman, H.; Huang, B.-S.; Liao, J.-Y.; Thorat, V. H.; Liao, Z.-Y.; Liu, Y.-H.; Yen, L.-T.; Hsieh, J.-C.;* Chuang, G. J.* Chem. Asian J. 2025, 20, e00969. \u201cMetal Free Synthesis of Seven-Membered Biaryl Sultams\u201d Thorat, V. H.; Chuang, Y.-C.; Hsieh, C.-H.;* Hsieh, J.-C.* Adv. Synth. Catal. 2025, 367, e202500231. \u201cNickel-Catalyzed Transannulation Reaction of 1,2,3,4-Benzothiatriazin-1,1(2H)-dioxide [&hellip;]<\/p>\n","protected":false},"author":24,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"wp-custom-template-member-empty-template","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"acf":[],"_links":{"self":[{"href":"\/chemistry\/index.php?rest_route=\/wp\/v2\/posts\/3772"}],"collection":[{"href":"\/chemistry\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"\/chemistry\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"\/chemistry\/index.php?rest_route=\/wp\/v2\/users\/24"}],"replies":[{"embeddable":true,"href":"\/chemistry\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=3772"}],"version-history":[{"count":11,"href":"\/chemistry\/index.php?rest_route=\/wp\/v2\/posts\/3772\/revisions"}],"predecessor-version":[{"id":8777,"href":"\/chemistry\/index.php?rest_route=\/wp\/v2\/posts\/3772\/revisions\/8777"}],"wp:attachment":[{"href":"\/chemistry\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=3772"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"\/chemistry\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=3772"},{"taxonomy":"post_tag","embeddable":true,"href":"\/chemistry\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=3772"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}