{"id":7,"date":"2013-03-14T23:07:20","date_gmt":"2013-03-14T15:07:20","guid":{"rendered":"http:\/\/wp.kmu.edu.tw\/mychang\/?page_id=7"},"modified":"2023-11-10T15:24:06","modified_gmt":"2023-11-10T07:24:06","slug":"%e7%a0%94%e7%a9%b6%e8%91%97%e4%bd%9c","status":"publish","type":"page","link":"https:\/\/wp.kmu.edu.tw\/mychang\/%e7%a0%94%e7%a9%b6%e8%91%97%e4%bd%9c\/","title":{"rendered":"\u7814\u7a76\u8457\u4f5c"},"content":{"rendered":"<ul>\n<li><span style=\"color: #ff0000\">Hsueh, N.-C.; <strong>Chang, M.-Y.*<\/strong> <em>Adv. Synth. Catal. <\/em><strong>2023<\/strong>, <em>365<\/em>, 544-554. \u201cPhotoinduced Synthesis of Bis-sulfonyl \u03b3-Arylated Ketones via DMAP\/DDQ-mediated Stereogenic Conjugated Addition of \u03b1-Sulfonyl Chalcones with Benzylic Sulfones\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\"><strong>Chang, M.-Y.*<\/strong>; Lin, C.-Y. <em>Adv. Synth. Catal. <\/em><strong>2023<\/strong>, <em>365<\/em>, 911-924. \u201cOne-pot Construction of Sulfonyl Benzonorcaradienes\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\"><strong>Chang, M.-Y.*<\/strong>; Lin, C.-Y. <em>Adv. Synth. Catal. <\/em><strong>2023<\/strong>, <em>365<\/em>, 1442-1448. \u201c(CF<sub>3<\/sub>CO)<sub>2<\/sub>O\/K<sub>2<\/sub>CO<sub>3<\/sub>-Mediated Synthesis of 3-Sulfonylchromones through Cyclocondensation of \u03b2-Ketosulfones and Carboxylic Acids\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\"><strong>Chang, M.-Y.*<\/strong>; Chen, K.-T.; Chen, H.-Y.* <em>Adv. Synth. Catal. <\/em><strong>2023<\/strong>, <em>365<\/em>, 2264-2270. \u201cGrignard Reagent-Mediated Regioselective 1,8-Addition of \u03b1-(2-Thienylidene)-\u03b2-ketosulfones\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\"><strong>Chang, M.-Y.*<\/strong>; Hsueh, N.-C. <em>Adv. Synth. Catal. <\/em><strong>2023<\/strong>, <em>365<\/em>, 2560-2567. \u201cConstruction of Sulfonyl Dibenzofused Medium-size Oxacycles via Bi(OTf)<sub>3<\/sub>-promoted Friedel-Crafts-type Annulation\u201d<\/span><\/li>\n<li><span style=\"color: #ff00ff\"><strong>Chang, M.-Y.*<\/strong>; Lin, C.-Y.; Chen, S.-M. <em>Adv. Synth. Catal. <\/em><strong>2022<\/strong>, <em>364<\/em>, 2629-2641. \u201cSynthesis of 1-Aryl Isoquinolinones or <em>o<\/em>-Diaryl Pyrimidines via Bismuth Triflate-Mediated Intermolecular Annulation of Arylacetic Acids with Nitroarylaldehydes or Trimethoxybenzene in the Presence of Acetonitrile\u201d<\/span><\/li>\n<li><span style=\"color: #ff00ff\"><strong>Chang, M.-Y.*<\/strong>; Lin, C.-Y. <em>Adv. Synth. Catal. <\/em><strong>2022<\/strong>, <em>364<\/em>, 3211-3224. \u201cBi(OTf)<sub>3<\/sub>-Catalyzed Cyclocondensation of Oxygenated Arylacetic Acids with Salicyl Alcohols. Synthesis of 5-Oxadibenzo[<em>a<\/em>,<em>d<\/em>]cycloocten-6-ones\u201d\u00a0<\/span><\/li>\n<li><span style=\"color: #ff00ff\">Hsueh, N.-C.; Chen, K.-T.;<strong> Chang, M.-Y.*<\/strong> <em>Adv. Synth. Catal. <\/em><strong>2022<\/strong>, <em>364<\/em>, 4110-4121.\u201cOne-pot Construction of Dibenzooxabicyclo[5.5.0]dodecanes\u201d\u00a0<\/span><\/li>\n<li><span style=\"color: #339966\"><strong>Chang, M.-Y.*<\/strong>; Chen, K.-T. <em>Adv. Synth. Catal. <\/em><strong>2021<\/strong>, <em>363<\/em>, 2594-2609. \u201cBi(OTf)<sub>3<\/sub>-Mediated (4+1) Annulation of \u03b1-Sulfonyl o-Hydroxyacetophenones with \u03b1-Hydroxy Arylketones to Access Sulfonyl 2-Aroylbenzofurans\u201d\u00a0<\/span><\/li>\n<li><span style=\"color: #ff0000\"><strong>Chang, M.-Y.*<\/strong>; Tsai, Y.-L.; Chang, Y.-L. <em>J. Org. Chem. <\/em><strong>2020<\/strong>, <em>85<\/em>, 1033-1043. \u201cGram-Scale Synthesis of 3-Sulfonyl Flavanones\u201d\u00a0<\/span><\/li>\n<li><span style=\"color: #ff0000\"><strong>Chang, M.-Y.*<\/strong>; Chen, K.-T.; Hsiao, Y.-T.; Chen, S.-M. <em>J. Org. Chem. <\/em><strong>2020<\/strong>, <em>85<\/em>, 3605-3616. \u201cAc<sub>2<\/sub>O-Mediated Dearylacetylative Dimerization of 2-Arylacetyl-1-naphthols. Synthesis of Naphtho[1,2-<em>b<\/em>]furan-3-ones\u201d\u00a0<\/span><\/li>\n<li><span style=\"color: #ff0000\"><strong>Chang, M.-Y.*<\/strong>; Tsai, Y.-L. <em>J. Org. Chem. <\/em><strong>2020<\/strong>, <em>85<\/em>, 5651-5659. \u201cOne-Pot Amberlyst 15-Controlled Cyclocondensation of Piperidines and 2-Formylpyrroles. Synthesis of 3,5-Dipyrrolylmethyl Pyridines\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\"><strong>Chang, M.-Y.*<\/strong>; Tsai, Y.-L.; Chen, H.-Y.* <em>J. Org. Chem. <\/em><strong>2020<\/strong>, <em>85<\/em>, 6897-6909. \u201cCuBr<sub>2<\/sub>-Mediated One-Pot Synthesis of Sulfonyl 9-Fluorenylidenes\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\">Hsueh, N.-C.; Tsai, M.-C.; <strong>Chang, M.-Y.*<\/strong> <em>Adv. Synth. Catal. <\/em><strong>2020<\/strong>, <em>362<\/em>, 4723-4735. \u201cOne-pot Access to Sulfonyl 2-Arylnaphthalenes via Wacker Oxidation of Sulfonyl <em>o<\/em>-Allylchalcones\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\">Hsueh, N.-C.; <strong>Chang, M.-Y.*<\/strong> <em>Adv. Synth. Catal. <\/em><strong>2020<\/strong>, <em>362<\/em>, 5736-5750. \u201cPdCl<sub>2<\/sub>\/CuCl<sub>2<\/sub>\/Bi(OTf)<sub>3<\/sub>-promoted Construction of Sulfonyl Dibenzooxabicyclo[3.3.1]nonanes and Arylnaphthalenes via Intramolecular Annulation of Sulfonyl <em>o<\/em>-Allylarylchromanones\u201d<\/span><\/li>\n<li><span style=\"color: #ff00ff\"><strong>Chang, M.-Y.*<\/strong>; Chen, H.-Y.; Tsai, Y.-L. <em>Org. Lett. <\/em><strong>2019<\/strong>, <em>21<\/em>, 1832-1836. \u201cNH<sub>2<\/sub>OH-HCl Mediated Umpolung \u03b1-Methylsulfonylation of \u03b1-Sulfonyl Ketones with Methylsulfoxides. Synthesis of \u03b1,\u03b2-Bis-sulfonyl Arylketones\u201d\u00a0<\/span><\/li>\n<li><span style=\"color: #ff00ff\"><strong>Chang, M.-Y.*<\/strong>; Chen, H.-Y.; Tsai, Y.-L. <em>J. Org. Chem. <\/em><strong>2019<\/strong>, <em>84<\/em>, 326-337. \u201cTemperature-Controlled Desulfonylative Condensation of \u03b1-Sulfonyl <em>o<\/em>-Hydroxyacetophenones and 2-Formyl Azaarenes. Synthesis of 2-Azaaryl Aurones and Flavones\u201d\u00a0<\/span><\/li>\n<li><span style=\"color: #993300\"><span style=\"color: #ff00ff\"><strong>Chang, M.-Y.*<\/strong>; Chen, H.-Y.; Tsai, Y.-L. <em>J. Org. Chem. <\/em><strong>2019<\/strong>, <em>84<\/em>, 443-449. \u201cIntramolecular Benzannulation of 3-Sulfonyl-2-benzylchromen-4-ones. Synthesis of Sulfonyl Dibenzooxabicyclo[3.3.1]nonanes\u201d<\/span>\u00a0 <\/span><\/li>\n<li><span style=\"color: #ff00ff\"><strong>Chang, M.-Y.*<\/strong>; Wu, Y.-S. <em>J. Org. Chem. <\/em><strong>2019<\/strong>, <em>84<\/em>, 3638-3646. \u201cHOAc-Mediated Cyclocondensation of 2-Formylazaarenes and Cyclic Amines. Synthesis of Pyrrolo[1,2-<em>a<\/em>]azaarenes\u201d<\/span><\/li>\n<li><span style=\"color: #ff00ff\"><strong>Chang, M.-Y.*<\/strong>; Chen, S.-M.; Hsiao, Y.-T. <em>J. Org. Chem. <\/em><strong>2019<\/strong>, <em>84<\/em>, 11687-11698. \u201cTrifluoroacetic Anhydride-Mediated One-Pot Synthesis of 1-Aryl Isochroman-3-ones <em>via<\/em> the Carboxy-Pictet-Spengler Reaction\u201d\u00a0<\/span><\/li>\n<li><span style=\"color: #ff00ff\"><strong>Chang, M.-Y.*<\/strong>; Wu, Y.-H.; Tsai, Y.-L.; Chen, H.-Y.* <em>J. Org. Chem. <\/em><strong>2019<\/strong>, <em>84<\/em>, 11699-11723. \u201cSynthesis of 2-Sulfonyl Indenes and Indanes\u201d \u00a0\u00a0<\/span><\/li>\n<li><span style=\"color: #ff00ff\">Hsueh, N.-C.; Tsai, M.-C.; <strong>Chang, M.-Y.*<\/strong>; Chen, H.-Y.* <em>J. Org. Chem. <\/em><strong>2019<\/strong>, <em>84<\/em>, 15915-15925. \u201cConstruction of Sulfonyl Dihydrobenzo[<em>c<\/em>]xanthen-7-ones Core via NH<sub>4<\/sub>OAc\/PdCl<sub>2<\/sub>\/CuCl<sub>2<\/sub>-Mediated Double Cyclocondensation of \u03b1-Sulfonyl <em>o<\/em>-Hydroxyacetophenones with 2-Allylbenzaldehydes\u201d<\/span><\/li>\n<li><span style=\"color: #008000\"><strong>Chang, M.-Y.*<\/strong>; Wu, Y.-S.; Chen, H.-Y. <em>Org. Lett. <\/em><strong>2018<\/strong>, <em>20<\/em>, 1824-1827. \u201cCuI Mediated Synthesis of Sulfonyl Benzofuran-3-ones and Chroman-4-ones\u201d <strong>\u00a0\u00a0<\/strong><\/span><\/li>\n<li><span style=\"color: #008000\"><strong>Chang, M.-Y.*<\/strong>; Chen, Y.-H.; Wang, H.-S. <em>J. Org. Chem. <\/em><strong>2018<\/strong>, <em>83<\/em>, 2361-2368. \u201cCu(OAc)<sub>2<\/sub> Mediated Synthesis of 3-Sulfonyl Chromen-4-ones\u201d <strong>\u00a0<\/strong><\/span><\/li>\n<li><span style=\"color: #008000\"><strong>Chang, M.-Y.*<\/strong>; Tsai, Y.-L. <em>J. Org. Chem. <\/em><strong>2018<\/strong>, <em>83<\/em>, 6798-6804. \u201cStereocontrolled Synthesis of 3-Sulfonyl Chroman-4-ols\u201d\u00a0<\/span><\/li>\n<li><span style=\"color: #008000\">Hsueh, N.-C.; Lai, K.-S.; <strong>Chang, M.-Y.*<\/strong> <em>J. Org. Chem. <\/em><strong>2018<\/strong>, <em>83<\/em>, 11415-11424. \u201cStereocontrolled Construction of 1-Vinylindanes via Intramolecular Cyclization of <em>o<\/em>-Cinnamyl Chalcones\u201d\u00a0<\/span><\/li>\n<li><span style=\"color: #008000\"><strong>Chang, M.-Y.*<\/strong>; Hsiao, Y.-T.; Lai, K.-S. <em>J. Org. Chem. <\/em><strong>2018<\/strong>, <em>83<\/em>, 14110-14119. \u201c<em>m<\/em>CPBA-Mediated Intramolecular Oxidative Annulation of <em>ortho<\/em>-Crotyl or Cinnamyl Arylaldehydes. Synthesis of Benzofused Five-, Six- and Seven-Membered Oxacycles\u201d\u00a0<\/span><\/li>\n<li><span style=\"color: #ff0000\">Chan, C.-K.; Tsai, Y.-L.; <strong>Chang, M.-Y.*<\/strong> <em>Org. Lett. <\/em><strong>2017<\/strong>, <em>19<\/em>, 1358-1361.\u201cConstruction of Nitrated Benzo[3.3.1]bicyclic Acetal\/ketal Core via Nitration of <em>o<\/em>-Carbonyl Allylbenzenes\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\">Chan, C.-K.; Tsai, Y.-L.; <strong>Chang, M.-Y.*<\/strong> <em>Org. Lett. <\/em><strong>2017<\/strong>, <em>19<\/em>, 1870-1873. \u201cCuI Mediated One-pot Cycloacetalization\/Ketalization of <em>o<\/em>-Carbonyl Allylbenzenes: Synthesis of Benzobicyclo[3.2.1]octane Core\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\">Chan, C.-K.; Chen, Y.-H.; Tsai, Y.-L.; <strong>Chang, M.-Y.*<\/strong> <em>J. Org. Chem. <\/em><strong>2017<\/strong>, <em>82<\/em>, 3317-3326. \u201cSynthesis of Substituted 1,6-Diarylnaphthalenes via a Tandem Claisen Rearrangement and Ene Reaction Protocol\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\">Chan, C.-K.; Hsueh, N.-C.; Tsai, Y.-L.; <strong>Chang, M.-Y.*<\/strong> <em>J. Org. Chem. <\/em><strong>2017<\/strong>, <em>82<\/em>, 7077-7084. \u201cBi(OTf)<sub>3<\/sub> Mediated Intramolecular Olefinic Cyclization: Synthesis of Substituted Aryl-Dihydronaphthalenes and Indenes\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\"><strong>Chang, M.-Y.*<\/strong>; Chen, H.-Y.; Wang, H.-S. <em>J. Org. Chem. <\/em><strong>2017<\/strong>, <em>82<\/em>, 10601-10610. \u201cRegiocontrolled Synthesis of \u03b1-Sulfonylmethyl <em>o<\/em>-Nitrostyrenes via ZnI<sub>2<\/sub>-Mediated Sulfonylation and AgNO<sub>2<\/sub>\/Pd(PPh<sub>3<\/sub>)<sub>4<\/sub>-Promoted <em>o<\/em>-Nitration\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\"><strong>Chang, M.-Y.*<\/strong>; Hsiao, Y.-T. <em>J. Org. Chem. <\/em><strong>2017<\/strong>, <em>82<\/em>, 11594-11602. \u201cH<sub>2<\/sub>SO<sub>4<\/sub> Mediated Stereocontrolled Annulation of Sulfonyl 4-Alkenols and Oxygenated Naphthalenes: One-Pot Synthesis of Sulfonyl Tetanthrenes\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\"><strong>Chang, M.-Y.*<\/strong>; Chen, H.-Y.; Chen, Y.-H. <em>J. Org. Chem. <\/em><strong>2017<\/strong>, <em>82<\/em>, 12631-12639. \u201cSynthesis of 2-Aryl-3-Sulfonylchromans via Knoevenagel Condensation and Reduction Protocol\u201d <\/span><\/li>\n<li><span style=\"color: #ff0000\">Hsueh, N.-C.; Chen, H.-Y.*; <strong>Chang, M.-Y.*<\/strong> <em>J. Org. Chem. <\/em><strong>2017<\/strong>, <em>82<\/em>, 13324-13332. \u201cConstruction of Sulfonyl Oxabenzo[3.3.1]bicyclic Core via Cyclocondensation of \u03b2-Ketosulfones and<em> o<\/em>-Formyl Allylbenzenes\u201d\u00a0 <\/span><\/li>\n<li><span style=\"color: #ff00ff\"><strong>Chang, M.-Y.*<\/strong>; Cheng, Y.-C. <em>Org. Lett. <\/em><strong>2016<\/strong>, <em>18<\/em>, 608-611. \u201cSynthesis of Substituted Tetralins and Benzosuberans via BF<sub>3<\/sub>\u00b7OEt<sub>2<\/sub> Mediated Formal (4+2) and (5+2) Stereocontrolled Cycloaddition of 4-Alkenols with Veratrol\u201d<\/span><\/li>\n<li><span style=\"color: #ff00ff\"><strong>Chang, M.-Y.*<\/strong>; Cheng, Y.-C. <em>Org. Lett. <\/em><strong>2016<\/strong>, <em>18<\/em>, 1682-1685. \u201cSynthesis of Substituted 1-Aryltetralins and 1-Arylnaphthalenes via (4+2) Annulation of \u03b2-Ketosulfones with Styryl Bromides\u201d <\/span><\/li>\n<li><span style=\"color: #ff00ff\">Chan, C.-K.; Chan, Y.-L.; Tsai, Y.-L.; <strong>Chang, M.-Y.*<\/strong> <em>J. Org. Chem. <\/em><strong>2016<\/strong>, <em>81<\/em>, 8112-8120. \u201cOne-Pot Synthesis of 2-Cyano-1,4-diketones: Applications to Synthesis of Cyanosubstituted Furans, Pyrroles and Dihydropyridazines\u201d <\/span><\/li>\n<li><span style=\"color: #ff00ff\">Chan, C.-K.; Tsai, Y.-L.; Chan, Y.-L.; <strong>Chang, M.-Y.*<\/strong> <em>J. Org. Chem. <\/em><strong>2016<\/strong>, <em>81<\/em>, 9836-9847. \u201cSynthesis of Substituted 2,3-Benzodiazepines\u201d<\/span><\/li>\n<li><span style=\"color: #008000\"><strong>Chang, M.-Y.*<\/strong>; Cheng, Y.-C.; Lu, Y.-J. <em>Org. Lett. <\/em><strong>2015<\/strong>, <em>17<\/em>, 1264-1267. \u201cBi(OTf)<sub>3<\/sub>-Mediated Cycloisomerization of \u03b3-Alkynyl Arylketones: Application to the Synthesis of Substituted Furans\u201d<\/span><\/li>\n<li><span style=\"color: #008000\"><strong>Chang, M.-Y.*<\/strong>; Cheng, Y.-C.; Lu, Y.-J. <em>Org. Lett. <\/em><strong>2015<\/strong>, <em>17<\/em>, 3142-3145. \u201cSynthesis of Substituted Benzenes via Bi(OTf)<sub>3<\/sub>-Mediated Intramolecular Carbonyl Allylation of \u03b1-Prenyl or \u03b1-Gernyl \u03b2-Arylketosulfones\u201d<\/span><\/li>\n<li><span style=\"color: #008000\"><strong>Chang, M.-Y.*<\/strong>; Cheng, Y.-C. <em>Org. Lett. <\/em><strong>2015<\/strong>, <em>17<\/em>, 5702-5705. \u201cBi(OTf)<sub>3<\/sub> Mediated <em>Exo<\/em>-Olefin Isomerization of \u03b1-Benzoyl \u03b2-Styrylsulfones\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\"><strong>Chang, M.-Y.*<\/strong>; Cheng, Y.-C.; Lu, Y.-J. <em>Org. Lett. <\/em><strong>2014<\/strong>, <em>16<\/em>, 6252-6255. \u201cOne-pot Access to Sulfonylmethyl Arylpyrroles via the Domino Aerobic Wacker-type Aminocyclization\/1,4-Sulfonyl Migration\u201d<\/span><\/li>\n<li><span style=\"color: #ff00ff\"><strong><b>Chang, M.-Y.*<\/b><\/strong>; Wu, M.-H.; Chen, Y.-L. <i>Org. Lett. <\/i><strong><b>2013<\/b><\/strong>, <i>15<\/i>, 2822-2825. \u201cOne-pot Synthesis of Substituted Tetrahydrocyclobuta[<i>a<\/i>]naphthalenes by Domino Aldol Condensation\/Olefin Migration\/Electrocyclization\u201d\u00a0\u00a0<\/span><\/li>\n<li><span style=\"color: #008000\"><b>Chang, M.-Y.*<\/b>; Lee, T.-W.; Wu, M.-H.\u00a0<i>Org. Lett.\u00a0<\/i><b>2012<\/b>,\u00a0<i>14<\/i>,\u00a02198-2201.\u00a0\u201cPolyphosphoric\u00a0Acid Promoted Synthesis of\u00a0Tetrahydrobenzo[<i>j<\/i>]fluoranthen-12-one\u201d<\/span><\/li>\n<li><span style=\"color: #008000\"><b>Chang, M.-Y.*<\/b>; Wu, M.-H.; Tai, H.-Y.\u00a0<i>Org. Lett.\u00a0<\/i><b>2012<\/b>,\u00a0<i>14<\/i>,\u00a03936-3939.\u00a0\u201cNH<sub>4<\/sub>OAc Mediated\u00a0Cyclocondensation\u00a0of 3-(<i>o<\/i>-Allylphenyl)pentane-1,5-dione: Synthesis of Tetracyclic\u00a0Benzofused\u00a0Azahomoisotwistane\u201d<\/span><\/li>\n<li><span style=\"color: #ff0000\"><b>Chang, M.-Y.*<\/b>; Lin, C.-H.; Chen, Y.-L.; Chang, C.-Y.; Hsu, R.-T.\u00a0<i>Org. Lett.\u00a0<\/i><b>2010<\/b>,\u00a0<i>12<\/i>, 1176-1179.\u00a0\u201cBF<sub>3<\/sub>-Promoted Synthesis of\u00a0Diarylhexahydrobenzo[<i>f<\/i>]isoquinoline\u201d<\/span><\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Hsueh, N.-C.; Chang, M.-Y.* Adv. Synth.  &hellip; <a href=\"https:\/\/wp.kmu.edu.tw\/mychang\/%e7%a0%94%e7%a9%b6%e8%91%97%e4%bd%9c\/\">\u95b1\u8b80\u5168\u6587 <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":14,"featured_media":0,"parent":0,"menu_order":1,"comment_status":"closed","ping_status":"closed","template":"onecolumn-page.php","meta":{"_exactmetrics_skip_tracking":false,"_exactmetrics_sitenote_active":false,"_exactmetrics_sitenote_note":"","_exactmetrics_sitenote_category":0,"footnotes":""},"class_list":["post-7","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/wp.kmu.edu.tw\/mychang\/wp-json\/wp\/v2\/pages\/7","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/wp.kmu.edu.tw\/mychang\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/wp.kmu.edu.tw\/mychang\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/wp.kmu.edu.tw\/mychang\/wp-json\/wp\/v2\/users\/14"}],"replies":[{"embeddable":true,"href":"https:\/\/wp.kmu.edu.tw\/mychang\/wp-json\/wp\/v2\/comments?post=7"}],"version-history":[{"count":70,"href":"https:\/\/wp.kmu.edu.tw\/mychang\/wp-json\/wp\/v2\/pages\/7\/revisions"}],"predecessor-version":[{"id":158,"href":"https:\/\/wp.kmu.edu.tw\/mychang\/wp-json\/wp\/v2\/pages\/7\/revisions\/158"}],"wp:attachment":[{"href":"https:\/\/wp.kmu.edu.tw\/mychang\/wp-json\/wp\/v2\/media?parent=7"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}