{"id":1098,"date":"2017-09-25T10:12:22","date_gmt":"2017-09-25T01:12:22","guid":{"rendered":"https:\/\/labs.eng.hokudai.ac.jp\/labo\/orgsynth\/?page_id=1098"},"modified":"2024-11-30T10:25:37","modified_gmt":"2024-11-30T01:25:37","slug":"taiga-yurino-achievements","status":"publish","type":"page","link":"https:\/\/c-mng.cwh.hokudai.ac.jp\/orgsynth.eng\/Root\/member\/taiga-yurino\/taiga-yurino-achievements","title":{"rendered":"\u696d\u7e3e\u30fc\u767e\u5408\u91ce\u5927\u96c5\u30fc"},"content":{"rendered":"<ul>\n<li>Papers<\/li>\n<\/ul>\n<ol>\n<li>&#8221;\u00a0 \u00a0 &#8221;<br \/>\nT. Yurino,* T. Ishikawa, T. Nakamura, T. Ohkuma* <em>in preparation<\/em><\/li>\n<li>&#8221;\u00a0 \u00a0 &#8221;<br \/>\nT. Yurino,* M. Ichihashi, R. Tani, T. Ohkuma* <em>in preparation<\/em><\/li>\n<li>&#8221;\u00a0 \u00a0 &#8221;<br \/>\nT. Yurino,* H. Hu, T. Yamamoto, T. Ohkuma* <em>in preparation<\/em><\/li>\n<li>&#8221;\u00a0 \u00a0 \u00a0&#8221;<br \/>\nT. Yurino,* K. Suzuki, A. Sasaki, T. Takashima, T. Ohkuma* <em>in preparation<\/em><\/li>\n<li>&#8221;\u00a0 \u00a0 \u00a0&#8221;<br \/>\nT. Yurino,* H. Yamashita, Y. Tange, T. Ohkuma* <em>in preparation<br \/>\n<\/em><\/li>\n<li>&#8221;\u00a0 \u00a0 \u00a0&#8221;<br \/>\nT. Yurino,* A. Hachiya, R. Saeki, T. Ohkuma* <em>in preparation<\/em><\/li>\n<li>Asymmetric Cyanation of \u03b1-Ketimino Ester Derivatives with Chiral Ru\u2013Li Combined Catalysts<br \/>\nT. Yurino, Zhen Wu, K. Suzuki, R. Nitta, Y. Sakaguchi, T. Ohkuma* <em>Org. Lett. <\/em><strong>2024<\/strong>, 26, 900\u2013905. (<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.3c04175\">link<\/a>)<\/li>\n<li>Asymmetric Hydrogenation of \u03b1-Alkyl-Substituted \u03b2-Keto Esters and Amides through Dynamic Kinetic Resolution<br \/>\nT. Yurino, R. Nishihara, T. Yasuda, S. Yang, N. Utsumi, T. Katayama, N. Arai, T. Ohkuma* <em>Org. Lett. <\/em><strong>2024<\/strong>, <em>accepted <\/em>(<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.3c04036\">link<\/a>)<\/li>\n<li>Ru(\u03b71-BH4)(daipena)(diphosphine): Ruthenabicyclic borohydride complexes for asymmetric hydrogenation of ketones and asymmetric formatl hydroamination of allylic alcohols under base-free conditions<br \/>\nT. Ishizaka, Y. Nakayama, T. Touge, Y. Yuki, K. Matsumura, T. Yurino, T. Ohkuma*\u00a0<em>Tetrahedron\u00a0<\/em><strong>2023<\/strong>,\u00a0<em>149<\/em>, 133705. (<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402023005070\">link<\/a>)<\/li>\n<li>Ag-Catalyzed Cyanomethylation of Amines Using Nitromethane as a C1 Source<br \/>\nT. Takashima, H. Ece, T. Yurino,* T. Ohkuma* <em>Org. Lett.\u00a0<\/em><strong>2023<\/strong>,\u00a0<em>25<\/em>, 6052\u20136055. (<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.3c02256?fbclid=IwAR0eCN5OlB0KI_Vw9xUVz6a3wknZhIEbM6yYQ0pJYR_NyyJTRkJFz5NOwkk\">link<\/a>)<\/li>\n<li>Asymmetric Hydrogenation of Amino Esters into Optically Active Amino Alcohols through Dynamic Kinetic Resolution Catalyzed by Ruthenabicyclic Complexes<br \/>\nH. Ishikawa, T. Yurino, R. Komatsu, M.-Y. Gao, N. Arai, T. Touge, K. Matsumura, T. Ohkuma*\u00a0<em>Org. Lett.\u00a0<\/em><strong>2023, <\/strong><em>25<\/em><strong>, <\/strong>2355\u20132360. (<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.3c00740?fbclid=IwAR2FWTtFR20RUe-6S9fPhE3Kmp_fy6aHaf2UCNjXOd8sihtq-CBW05hTE3I\">link<\/a>)<\/li>\n<li>\u00a0Development of Catalytic Isocyanation via Precise Reactivity Control of Ambident Reagent<br \/>\nT. Yurino,* T. Ohkuma* <em>J. Synth. Org. Chem. Jpn. <\/em><strong>2023, <\/strong><em>81<\/em>, 235\u2013243.(<a href=\"https:\/\/www.jstage.jst.go.jp\/article\/yukigoseikyokaishi\/81\/3\/81_235\/_article\/-char\/ja\">link<\/a>)<\/li>\n<li>\u00a0Potassium Alkoxide as an Efficient Catalyst for Nucleophilic Perfluoroalkylation: Attempt at Anion-Controlled Enantioselective Insertion of CF<sub>3<\/sub> Group<br \/>\nT. Yurino,* H. Yamashita, Y. Shan, Z. Wu, T. Ohkuma*\u00a0<em>Synlett\u00a0<\/em><strong>2022<\/strong>,\u00a0<em>33<\/em>, 1739\u20131744.(<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/html\/10.1055\/a-1914-1518\">link<\/a>)<\/li>\n<li>\u300e\u30b1\u30a4\u7d20\u304c\u89e6\u5a92\u3059\u308b\u6709\u6a5f\u5408\u6210\u5316\u5b66\u306e\u65b0\u5c55\u958b\u300f<br \/>\n\u767e\u5408\u91ce\u5927\u96c5\u3000\u5316\u5b66\u3068\u5de5\u696d\u30002022\u5e744\u6708\u53f7<\/li>\n<li>\u00a0Aerobic Allylic Amination Catalyzed by Pd(OAc)2\/P(OPh)3 System with Low Catalyst Loading<br \/>\nT. Yurino,* S. Saito, M. Ichihashi, T. Ohkuma* <em>J. Org. Chem.\u00a0<\/em><strong>2022<\/strong>, <em>87<\/em>, 2864\u20132872.\u00a0(<a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.joc.1c02768\">link<\/a>)<\/li>\n<li>\u00a0Palladium-Catalyzed Nucleophilic Isocyanation for the <span style=\"letter-spacing: -0.02em;\">Synthesis of \u03b1-Aryl-\u03b1-isocyanoacetoamide Derivatives<\/span>&#8221;<br \/>\nT. Yurino,* Y. Tange, T. Ohkuma*\u00a0<em>Bull. Chem. Soc. Jpn.\u00a0<\/em><strong>2021<\/strong>, <em>94<\/em>, 2155\u20132161. (<a href=\"https:\/\/www.journal.csj.jp\/doi\/full\/10.1246\/bcsj.20210214\">link<\/a>)<\/li>\n<li>Silyl Cyanopalladate-Catalyzed Friedel\u2013Crafts-type Cyclization Affording 3-Aryloxindole Derivatives&#8221;<br \/>\nH. Ece, Y. Tange, T. Yuino,* T. Ohkuma*\u00a0<em>Synlett<\/em> <strong>2021<\/strong>, <em>32<\/em>, 935\u2013939. (<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/html\/10.1055\/a-1373-7017\">link<\/a>)<\/li>\n<li>Ag2O-catalysed Nucleophilic Isocyanation: Selective Formation of Less-Stable Benzylic Isonitriles<br \/>\nT. Yurino,* Y. Tange, R. Tani, T. Ohkuma*\u00a0<em>Org. Chem. Front.<\/em> <strong>2020<\/strong>,\u00a0<em>7<\/em>, 1308\u20131313.\u00a0(<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2020\/qo\/d0qo00336k?fbclid=IwAR3CeLGQM9HHA2GQJ5rYETNBvj1zJG9Gs6k6WIZ2zDrWL_apqwpiXBylBHU#!divAbstract\">link<\/a>) (Front Cover Picture)<\/li>\n<li>\u00a0Nucleophilic Isocyanation<br \/>\nT. Yurino,* T. Ohkuma* <em>ACS Omega\u00a0<\/em><strong>2020<\/strong>, 4719\u20134724 (<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsomega.9b04073\">link<\/a>)<\/li>\n<li>\u00a0Selective Conversion of Benzylic Phosphates into Diarylmethanes through Al(OTf)3-Catalyzed Friedel\u2013Crafts-type Benzylation<br \/>\nT. Yurino,* A. Hachiya, K. Suzuki, T. Ohkuma*\u00a0<em>Eur. J. Org. Chem. <\/em><strong>2020<\/strong>,\u00a02020, 2225\u20132232. (<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/ejoc.202000077\">link<\/a>)<\/li>\n<li>\u00a0Friedel\u2013Crafts-type Allylation of Phenol Derivatives Catalyzed by Silyl Cyanometallates Generated <em>In Situ<\/em><br \/>\nT. Yurino,* H. Ece, T. Ohkuma,\u00a0<em>Asian J. Org. Chem<\/em>. <strong>2020<\/strong>, 9, 557\u2013560. (<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/ajoc.202000023?fbclid=IwAR2C9RjM9nkQW5Meh5Ban9kgmA2D4_vWAgk6H1Cjd4qdxZZ5OlVMr5tLYuc\">link<\/a>)<\/li>\n<li>\u00a0Metal-free Reductive Deoxygenation of Sulfoxides by an Organosilicon Reductant, 1,1&#8242;-Bis(trimethylsilyl)-1H,1&#8217;H-4,4&#8242;-bipyridinylidene<br \/>\nA. Battacharjee, H. Hosoya, T. Yurino, H. Tsurugi, K. Mashima\u00a0<em>Chem. Lett.<\/em>\u00a0<strong>2019<\/strong>, <em>48<\/em>, 888\u2013890. (<a href=\"https:\/\/www.journal.csj.jp\/doi\/abs\/10.1246\/cl.190340\">link<\/a>)<\/li>\n<li>\u00a0Pd-Catalyzed Allylic Isocyanation: Nucleophilic <em>N<\/em>-Terminus Substitution of Ambident Cyanide<br \/>\nT. Yurino,* R. Tani, T. Ohkuma*\u00a0<em>ACS Catal.\u00a0<\/em><strong>2019<\/strong><em>,\u00a09<\/em>, 4434\u20134440. (<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.9b00858\">link<\/a>)<\/li>\n<li>\u00a0Nickel-catalyzed cyanation of aryl halides and triflates using actonitrile <em>via<\/em> C\u2013CN bond cleavage assisted by 1,4-bis(trimethylsilyl)-2,3,5,6-tetramethyl-1,4-dihydropyrazine<br \/>\nY. Ueda, N. Tsujimoto, T. Yurino, H. Tsurugi, K. Mashima\u00a0<em>Chem. Sci.\u00a0<\/em><strong>2019<\/strong>,\u00a0<em>10<\/em>, 994\u2013999. (<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlehtml\/2019\/sc\/c8sc04437f\">link<\/a>)<\/li>\n<li>\u00a0Planer and Bent BN-Embedded <em>p<\/em>-Quinodimethanes Synthesized by Transmetallation of Bis(trimethylsilyl)pyrazines with Chloroborane<br \/>\nM. Noguchi, K. Suzuki, J. Kobayashi, T. Yurino, H. Tsurugi, K. Mashima, M. Yamashita\u00a0<em>Organometallics <\/em><strong>2018<\/strong>,\u00a0<em>37<\/em>, 1833\u20131836. (<a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.organomet.8b00294\">link<\/a>)<\/li>\n<li>\u00a0Enantioselective Cyanosilylation of Alkynyl Ketones Catalyzed by Combined Systems Consisting of Chiral Ruthenium(II) Complex and Lithium Phenoxide<br \/>\nT. Ohkuma,* N. Kurono, Y. Sakaguchi, K. Yamauchi, T. Yurino <em>Adv. Synth. Catal. <\/em><strong>2018<\/strong>,\u00a0<em>360<\/em>, 1517\u20131522. (<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/adsc.201701593\">link<\/a>)<\/li>\n<li><em>\u00a0In situ <\/em>generation of\u00a0<em>N<\/em>-Boc-protected alkenyl imines: controlling the\u00a0<em>E<\/em>\/<em>Z\u00a0<\/em>geometry of alkenyl moieties in the Mukaiyama-Mannich reaction<br \/>\nJ.\u2013F. Bai, H. Sasagawa, T. Yurino, T. Kano,* K. Maruoka*\u00a0<em>Chem. Commun.\u00a0<\/em><strong>2017<\/strong>,\u00a0<em>53,<\/em>\u00a08203\u20138206. (<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlehtml\/2017\/cc\/c7cc04674j\">link<\/a>)<\/li>\n<li>Undirected Dehydrogenative Silylation of Aromatic C\u2013H Bond<br \/>\nT. Yurino\u00a0<em>J. Synth. Org. Chem. Jpn.\u00a0<\/em><strong>2017<\/strong>,\u00a0<em>75<\/em>, 64\u201365. (<a href=\"https:\/\/www.jstage.jst.go.jp\/article\/yukigoseikyokaishi\/75\/1\/75_64\/_article\">link<\/a>)<\/li>\n<li><em>N-<\/em>Boc-aminals as easily accessible precursors for less accessible\u00a0<em>N<\/em>-Boc-imines: facile synthesis of optically active propargylamine derivatives using Mannich-type reactions<br \/>\nT. Yurino, Y. Aota, D. Asakawa, T. Kano, K. Maruoka*\u00a0<em>Tetrahedron\u00a0<\/em><strong>2016<\/strong>,\u00a0<em>72<\/em>, 3687\u20133700. (<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S004040201630206X\">link<\/a>)<\/li>\n<li>Salt-Free Reduction of Nonprecious Transition-Metal Compounds: Generation of Amorphous Ni Nanoparticles for Catalytic C\u2013C Bond Formation<br \/>\nT. Yurino, Y. Ueda, Y. Shimizu, S. Tanaka, H. Nishiyama, H. Tsurugi, K. Sato,* K. Mashima*\u00a0<em>Angew. Chem. Int. Ed\u00a0<\/em><strong>2015<\/strong>,\u00a0<em>54<\/em>, 14437\u201314441. (<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201507902\/full\">link<\/a>)<\/li>\n<li>Organocatalytic Asymmetric Synthesis of Propargylamines with Two Adjacent Stereocenters: Mannich-Type Reactions of In Situ Generated\u00a0<em>C<\/em>-Alkynyl Imines with \u03b2-Keto Esters<br \/>\nT. Kano, T. Yurino, K. Maruoka*\u00a0<em>Angew. Chem. Int. Ed.\u00a0<\/em><strong>2013<\/strong>,\u00a0<em>52<\/em>, 11509\u201311512. (<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201304963\/full\">link<\/a>)<\/li>\n<li>Acid-Catalyzed\u00a0<em>In situ\u00a0<\/em>Generation of Less Accessible or Unprecedented\u00a0<em>N<\/em>-Boc Imines from\u00a0<em>N<\/em>-Boc Aminals<br \/>\nT. Kano, T. Yurino, D. Asakawa, K. Maruoka*\u00a0<em>Angew. Chem. Int. Ed.\u00a0<\/em><strong>2013<\/strong>,\u00a0<em>52<\/em>, 5532\u20135534. (<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201300231\/full\">link<\/a>)<\/li>\n<li>Enantioselective construction of quaternary\u00a0<em>N<\/em>-heterocycles by palladium-catalysed decarboxylative allylic alkylation of lactams<br \/>\nD. C. Behenna, Y. Liu, T. Yurino, J. Kim, D. E. White, S. C. Virgil, B. M. Stoltz*\u00a0<em>Nature Chem.\u00a0<\/em><strong>2012<\/strong>,\u00a0<em>4<\/em>, 130\u2013133. (<a href=\"http:\/\/www.nature.com\/nchem\/journal\/v4\/n2\/full\/nchem.1222.html?foxtrotcallback=true\">link<\/a>)<\/li>\n<li>Palladium-Catalyzed Dimerization of\u00a0<em>meso-<\/em>Bromoporphyrins: Highly Regioselective\u00a0<em>meso-<\/em>\u03b2 Coupling through Unprecedented Remote C\u2013H Bond Cleavage<br \/>\nS. Tokuji, T. Yurino, N. Aratani, H. Shinokubo,* A. Ohsuka*\u00a0<em>Chem. Eur. J.\u00a0<\/em><strong>2009<\/strong>,\u00a0<em>15<\/em>, 12208\u201312211. (<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/chem.200902143\/full\">link<\/a>)<\/li>\n<li>Catalytic enantioselective construction of all-carbon quaternary stereocenters by an organocatalytic Diels-Alder reaction of \u03b1-substituted \u03b1,\u03b2-unsaturated aldehydes<br \/>\nT. Kano, Y. Tanaka, K. Osawa, T. Yurino, K. Maruoka*\u00a0<em>Chem. Commun.\u00a0<\/em><strong>2008<\/strong>,\u00a01956\u20131958. (<a href=\"http:\/\/pubs.rsc.org\/is\/content\/articlehtml\/2009\/cc\/b819034h\">link<\/a>)<\/li>\n<li>\u00a0Facile Synthesis of Structurally Diverse 3,3\u2032-Disubstituted 1,1\u2032-Binaphthyl-2,2\u2032-diamines in Optically Pure Forms<br \/>\nT. Kano, Y. Tanaka, K. Osawa, T. Yurino, K. Maruoka*\u00a0<em>J. Org. Chem.\u00a0<\/em><strong>2008<\/strong>,\u00a0<em>73<\/em>, 7387\u20137389. (<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jo8011368\">link<\/a>)<\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n<ul>\n<li>Reviews<\/li>\n<\/ul>\n<ol>\n<li>Development of Catalytic Isocyanation via Precise Reactivity Control of Ambident Reagent<br \/>\nT. Yurino,* T. Ohkuma* <em>J. Synth. Org. Chem. Jpn. <\/em><strong>2023, <\/strong><em>81<\/em>, 235\u2013243.(<a href=\"https:\/\/www.jstage.jst.go.jp\/article\/yukigoseikyokaishi\/81\/3\/81_235\/_article\/-char\/ja\">link<\/a>)<\/li>\n<li>\u300e\u30b1\u30a4\u7d20\u304c\u89e6\u5a92\u3059\u308b\u6709\u6a5f\u5408\u6210\u5316\u5b66\u306e\u65b0\u5c55\u958b\u300f<br \/>\n\u767e\u5408\u91ce\u5927\u96c5<br \/>\n\u5316\u5b66\u3068\u5de5\u696d\uff14\u6708\u53f7\u3000\u652f\u90e8\u767a\u8a71\u984c<\/li>\n<li>&#8220;Nucleophilic Isocyanation&#8221;<br \/>\nT. Yurino, T. Ohkuma <em>ACS Omega\u00a0<\/em><strong>2020<\/strong>, <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsomega.9b04073\">4719\u20134724<\/a><\/li>\n<li>Undirected Dehydrogenative Silylation of Aromatic C\u2013H Bond<br \/>\nT. Yurino\u00a0<em>J. Synth. Org. Chem. Jpn.\u00a0<\/em><strong>2017<\/strong>,\u00a0<em>75<\/em>, <a href=\"https:\/\/www.jstage.jst.go.jp\/article\/yukigoseikyokaishi\/75\/1\/75_64\/_article\">64\u201365<\/a><\/li>\n<li>\u300e\u6c34\u304b\u3089\u6c34\u7d20\u3092\u53d6\u308a\u51fa\u3057\u3066\u201d\u79fb\u3057\u66ff\u3048\u308b\u201d\u300f<br \/>\n\u767e\u5408\u91ce\u5927\u96c5<br \/>\n\u6708\u520a\u5316\u5b66\u30002017\u5e742\u6708\u53f7\u63b2\u8f09<\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n<ul>\n<li>Book and Book Chapter<\/li>\n<\/ul>\n<ol>\n<li>Comprehensive Chirality 2nd Edition: Reference Module in Chemistry, Molecular Sciences and Chemical Engineering<br \/>\nT. Yurino, T. Ohkuma Reduction: Asymmetric Hydrogenation and Transfer Hydrogenation of C=O Bonds (<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/B9780323906449000664\">link<\/a>)<\/li>\n<li>\u300c\u6709\u6a5f\u5408\u6210\u306e\u305f\u3081\u306e\u65b0\u89e6\u5a92\u53cd\u5fdc101\u300d \u767e\u5408\u91ce\u5927\u96c5\u3001\u5927\u718a\u6bc5<br \/>\n17. \u30ab\u30eb\u30dc\u30cb\u30eb\u57fa\u306e\u30b7\u30a2\u30ce\u5316<br \/>\n39. \u30a2\u30eb\u30b1\u30f3\u3001\u30a2\u30eb\u30ad\u30f3\u306e\u30b7\u30a2\u30ce\u5b98\u80fd\u57fa\u5316<br \/>\n40. \u4e0d\u6589Strecker\u53cd\u5fdc<\/li>\n<li>Atropisomerism and Axial Chirality (Ed. J. M. Lassaletta): Chapter 3. T. Yurino, T. Ohkuma Axially Chiral\u00a0<em>P<\/em>,<em>P<\/em>-Ligands for Asymmetric Metal-Catalyzed Reactions. (2019\/06)<\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n<ul>\n<li>Main Theme<\/li>\n<\/ul>\n<ol>\n<li>\u89e6\u5a92\u7684\u30a4\u30bd\u30b7\u30a2\u30ce\u5316\u53cd\u5fdc\u306e\u958b\u767a<\/li>\n<li>\u30a4\u30bd\u30cb\u30c8\u30ea\u30eb\u3001\u7279\u306b\u3001\u4e0d\u98fd\u548c\u30a4\u30bd\u30cb\u30c8\u30ea\u30eb\u3092\u57fa\u8cea\u3068\u3059\u308b\u65b0\u5947\u6709\u6a5f\u5408\u6210\u53cd\u5fdc\u306e\u5b9f\u73fe<\/li>\n<li>\u5927\u6c17\u89e3\u653e\u7cfb\u3001\u4f4e\u89e6\u5a92\u91cf\u3067\u5b9f\u73fe\u3059\u308b\u3001\u771f\u306b\u5b9f\u7528\u7684\u306a\u6709\u6a5f\u5408\u6210\u53cd\u5fdc\u306e\u958b\u767a<\/li>\n<li>\u9077\u79fb\u91d1\u5c5e\u89e6\u5a92\u3092\u7528\u3044\u305f\u3001\u5185\u5728\u6027\u5b98\u80fd\u57fa\u3092\u6a19\u7684\u3068\u3059\u308b\u751f\u4f53\u5171\u5f79\u53cd\u5fdc\u306e\u5b9f\u73fe<\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n<ul>\n<li>Grants<\/li>\n<\/ul>\n<ol>\n<li>JST \u6226\u7565\u7684\u5275\u9020\u7814\u7a76\u63a8\u9032\u4e8b\u696d \u3055\u304d\u304c\u3051<br \/>\n\u70ad\u7d20\u30fb\u7a92\u7d20\u5faa\u74b0\u3092\u5b9f\u73fe\u3059\u308b\u30b7\u30a2\u30cb\u30c9\u306e\u975e\u53e4\u5178\u7684\u8cc7\u6e90\u5316\u6cd5\u306e\u958b\u62d3<br \/>\n2024.10\u20132028.3<\/li>\n<li>\u57fa\u76e4\u7814\u7a76(C)<br \/>\n\u5b98\u80fd\u6027\u30a4\u30bd\u30cb\u30c8\u30ea\u30eb\u306e\u89e6\u5a92\u7684\u5408\u6210\u6cd5\u3068\u6d3b\u7528<br \/>\n2024.4\u20132027.3 \uff08\u7814\u7a76\u4ee3\u8868\uff09<\/li>\n<li>\u8c4a\u7530\u7406\u7814\u30b9\u30ab\u30e9\u30fc\u3000\u30b9\u30ab\u30e9\u30fc\u5171\u540c\u7814\u7a76<br \/>\n\u9ad8\u3072\u305a\u307f\u5316\u5408\u7269\u306e\u7cbe\u5bc6\u5206\u5b50\u5408\u6210\u306b\u57fa\u3065\u304f\u30e1\u30ab\u30ce\u30af\u30ed\u30df\u30c3\u30af\u30dd\u30ea\u30de\u30fc\u306e\u958b\u767a<br \/>\n2023.4\u20132024.3 \uff08\u5171\u540c\u7814\u7a76\u30fb\u5171\u540c\u4ee3\u8868\uff09<\/li>\n<li>NEDO \u5b98\u6c11\u306b\u3088\u308b\u82e5\u624b\u7814\u7a76\u8005\u767a\u6398\u652f\u63f4\u4e8b\u696d\u3000\u30de\u30c3\u30c1\u30f3\u30b0\u30b5\u30dd\u30fc\u30c8\u30d5\u30a7\u30fc\u30ba<br \/>\n\u30b7\u30a2\u30cb\u30c9\u306e\u5316\u5b66\u9078\u629e\u6027\u5236\u5fa1\u306b\u57fa\u3065\u304f\u9ad8\u4ed8\u52a0\u4fa1\u5024\u5316\u5408\u7269\u306e\u52b9\u7387\u7684\u5408\u6210\u624b\u6cd5\u306e\u958b\u767a<br \/>\n2022.9\u20132023.9\u3000\uff08\u7814\u7a76\u4ee3\u8868\uff09<\/li>\n<li>\u8c4a\u7530\u7406\u7814\u30b9\u30ab\u30e9\u30fc\u3000\u30b9\u30ab\u30e9\u30fc\u5171\u540c\u7814\u7a76<br \/>\n\u7cbe\u5bc6\u5206\u5b50\u5408\u6210\u3092\u57fa\u76e4\u3068\u3059\u308b\u9769\u65b0\u7684\u591a\u5b54\u8cea\u6709\u6a5f\u7d50\u6676\u306e\u5275\u88fd<br \/>\n2021.4\u20132022.9\uff08\u5171\u540c\u7814\u7a76\u30fb\u5171\u540c\u4ee3\u8868\uff09<\/li>\n<li>\u4e0a\u539f\u8a18\u5ff5\u751f\u547d\u79d1\u5b66\u8ca1\u56e3\u30002020\u5e74\u5ea6\u3000\u7814\u7a76\u5968\u52b1\u91d1<br \/>\n\u5171\u901a\u539f\u6599\u3092\u7528\u3044\u305f\u30d4\u30ed\u30fc\u30eb\u3001\u30d4\u30ea\u30b8\u30f3\u306e\u5206\u5c90\u7684\u5408\u6210\u6cd5<br \/>\n2021.1\u20132022.3\uff08\u7814\u7a76\u4ee3\u8868\uff09<\/li>\n<li>\u4ee4\u548c\uff12\u5e74\u5ea6FCC\u82e5\u624b\u30d5\u30a3\u30fc\u30b8\u30d3\u30ea\u30c6\u30a3\u30b9\u30bf\u30c7\u30a3\u652f\u63f4\u4e8b\u696d<br \/>\n\u30d5\u30eb\u30aa\u30ed\u30a2\u30eb\u30ad\u30eb\u57fa\u3092\u6709\u3059\u308b\u30d3\u30cb\u30eb\u304a\u3088\u3073\u30b8\u30a8\u30cb\u30eb\u30a4\u30bd\u30cb\u30c8\u30ea\u30eb\u985e\u306e\u52b9\u7387\u7684\u5408\u6210\u6cd5\u306e\u958b\u767a<br \/>\n2020.6\u20132021.3\uff08\u7814\u7a76\u4ee3\u8868\uff09<\/li>\n<li>\u8c4a\u7530\u7406\u7814\u30b9\u30ab\u30e9\u30fc<br \/>\n\u8907\u6570\u306e\u30a2\u30f3\u30d3\u30c7\u30f3\u30c8\u53cd\u5fdc\u5264\u306e\u540c\u6642\u7cbe\u5bc6\u5236\u5fa1\u306b\u3088\u308b\u69cb\u9020\u7570\u6027\u4f53\u306e\u4f5c\u308a\u5206\u3051<br \/>\n2020.4\u20132021.3\uff08\u7814\u7a76\u4ee3\u8868\uff09<\/li>\n<li>\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u3000\u30bb\u30f3\u30c8\u30e9\u30eb\u785d\u5b50\u3000\u7814\u7a76\u4f01\u753b\u8cde<br \/>\n\u89e6\u5a92\u7684\u8131\u30d5\u30c3\u7d20\u5316\u30a4\u30bd\u30b7\u30a2\u30ce\u5316\u53cd\u5fdc\u306e\u958b\u767a<br \/>\n2020.4\u20132021.3\uff08\u7814\u7a76\u4ee3\u8868\uff09<\/li>\n<li>\u82e5\u624b\u7814\u7a76<br \/>\n\u4e0d\u98fd\u548c\u30a4\u30bd\u30cb\u30c8\u30ea\u30eb\u306e\u89e6\u5a92\u7684\u5408\u6210\u6cd5\u306e\u958b\u767a\u3068\u65b0\u5947\u53cd\u5fdc\u3078\u306e\u5c55\u958b<br \/>\n2019.4\u20132021.3\u3000\uff08\u7814\u7a76\u4ee3\u8868\uff09<\/li>\n<li>\u57fa\u76e4\u7814\u7a76\uff08A\uff09<br \/>\n\u975e\u5bfe\u79f0\u7dfb\u5bc6\u53cd\u5fdc\u7a7a\u9593\u306b\u3088\u308b\u4e0d\u6589\u30db\u30a6\u7d20\u5316<br \/>\n2018.4\u20132019.3\u3000\uff08\u5206\u62c5\uff1a\u7814\u7a76\u4ee3\u8868\u3000\u4f0a\u85e4\u8087\u3000\u6559\u6388\uff09<\/li>\n<li>\u5e73\u6210\uff12\uff19\u5e74\u5ea6\u3000\u4f4f\u53cb\u8ca1\u56e3\u3000\u57fa\u790e\u79d1\u5b66\u7814\u7a76\u52a9\u6210<br \/>\n\u30b7\u30a2\u30f3\u5316\u7269\u30a4\u30aa\u30f3\u3092\u7a92\u7d20\u6e90\u3068\u3059\u308b\u3001\u30a2\u30df\u30ce\u9178\u8a98\u5c0e\u4f53\u306e\u65b0\u898f\u89e6\u5a92\u7684\u5408\u6210\u6cd5<br \/>\n2017.11\u20132019.03\u3000\uff08\u7814\u7a76\u4ee3\u8868\uff09<\/li>\n<li>\u5e73\u6210\uff12\uff18\u5e74\u5ea6FCC\u82e5\u624b\u30d5\u30a3\u30fc\u30b8\u30d3\u30ea\u30c6\u30a3\u30b9\u30bf\u30c7\u30a3\u652f\u63f4\u4e8b\u696d<br \/>\n\u533b\u85ac\u54c1\u5408\u6210\u3092\u5fd7\u5411\u3057\u305f\u3001\u30ab\u30eb\u30dc\u30cb\u30eb\u5316\u5408\u7269\u306e\u9ad8\u30a8\u30ca\u30f3\u30c1\u30aa\u9078\u629e\u7684\u30c8\u30ea\u30d5\u30eb\u30aa\u30ed\u30e1\u30c1\u30eb\u5316\u53cd\u5fdc<br \/>\n2016.09\u20132017.03\u3000\uff08\u7814\u7a76\u4ee3\u8868\uff09<\/li>\n<li>\u82e5\u624b\u7814\u7a76\uff08B\uff09<br \/>\n\u6709\u6a5f\u30b1\u30a4\u7d20\u5316\u5408\u7269\u304b\u3089\u306e\u96fb\u5b50\u79fb\u52d5\u306b\u57fa\u3065\u304f\u3001\u542b\u9178\u7d20\u6709\u6a5f\u5316\u5408\u7269\u306e\u76f4\u63a5\u7684\u5909\u63db\u53cd\u5fdc\u306e\u958b\u767a<br \/>\n2016.04\uff0d2019.03\u3000\uff08\u7814\u7a76\u4ee3\u8868\uff09<\/li>\n<li>\u7279\u5225\u7814\u7a76\u54e1\u5968\u52b1\u8cbb\uff08DC1\uff09<br \/>\n\u8ef8\u4e0d\u6589\u30d3\u30a2\u30ea\u30fc\u30eb\u30b8\u30a2\u30df\u30f3\u89e6\u5a92\u306e\u958b\u767a\u3068\u4e0d\u6589\u53cd\u5fdc\u3078\u306e\u5fdc\u7528<br \/>\n2010.04\u20132013.03\u3000\uff08\u7814\u7a76\u4ee3\u8868\uff09<\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n<ul>\n<li>Patents<\/li>\n<\/ul>\n<ol>\n<li>\u30a2\u30ea\u30eb\u30a4\u30bd\u30b7\u30a2\u30cb\u30c9\u985e\u306e\u88fd\u9020\u65b9\u6cd5<br \/>\n\u5927\u718a\u6bc5\u3001\u767e\u5408\u91ce\u5927\u96c5<br \/>\n\u7279\u98582017-035319\uff08\u7279\u8a31\u7b2c6871540\u53f7\uff09<\/li>\n<li>\u9084\u5143\u5264\u304a\u3088\u3073\u305d\u308c\u3092\u7528\u3044\u305f\u91d1\u5c5e\u306e\u88fd\u9020\u65b9\u6cd5<br \/>\n\u6c38\u7530\u76f4\u4eba\u3001\u771f\u5cf6\u548c\u5fd7\u3001\u5292\u96bc\u4eba\u3001\u767e\u5408\u91ce\u5927\u96c5\u3001\u9f4a\u85e4\u8f1d\u5f66\u3001\u68da\u6a4b\u5b8f\u5c06\u3001\u897f\u5c71\u60a0\u3001\u5ddd\u5317\u5065\u4eba<br \/>\n\u7279\u958b2016-124824\uff08\u7279\u8a31\u7b2c6329067\u53f7\uff09<\/li>\n<li>\u542b\u56db\u7d1a\u30d8\u30c6\u30ed\u539f\u5b50\u5316\u5408\u7269<br \/>\nD. C. Behenna, B. M. Stoltz, S. C. Virgil, D. E. White, \u767e\u5408\u91ce\u5927\u96c5, Y. Liu, D. Duquette, C. Eidamshaus<br \/>\n\u7279\u88682014-523427\uff08\u7279\u8a31\u7b2c6061923\u53f7\uff09<\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n<ul>\n<li>Prizes<\/li>\n<\/ul>\n<ol>\n<li>\u4ee4\u548c5\u5e74\u5ea6\u3000\u5de5\u5b66\u7814\u7a76\u9662\u82e5\u624b\u6559\u54e1\u5968\u52b1\u8cde (2024)<\/li>\n<li>\u65e5\u672c\u5316\u5b66\u4f1a\u5317\u6d77\u9053\u652f\u90e8\u652f\u90e8\u5968\u52b1\u8cde (2023)<\/li>\n<li>\u8c4a\u7530\u7406\u7814\u30b9\u30ab\u30e9\u30fc\u3000\u52a9\u6210\u5bfe\u8c61\u8005 (2020)<\/li>\n<li>\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u3000\u30bb\u30f3\u30c8\u30e9\u30eb\u785d\u5b50\u3000\u7814\u7a76\u4f01\u753b\u8cde (2019)<\/li>\n<li>Reaxys PhD Prize 2014<\/li>\n<li>\u5927\u6d25\u4f1a\u8b70\u30a2\u30ef\u30fc\u30c9\u30d5\u30a7\u30ed\u30fc (No.45)<\/li>\n<li>\u6709\u6a5f\u5408\u6210\u82e5\u624b\u30bb\u30df\u30ca\u30fc\u3000\u512a\u79c0\u7814\u7a76\u767a\u8868\u8cde (2012)<\/li>\n<li>\u65e5\u672c\u5316\u5b66\u4f1a\u7b2c\uff19\uff12\u6625\u5b63\u5e74\u4f1a\u3000\u5b66\u751f\u8b1b\u6f14\u8cde (2012)<\/li>\n<li>\u65e5\u672c\u5b66\u8853\u632f\u8208\u4f1a\u7279\u5225\u7814\u7a76\u54e1 (DC1) (2010)<\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n<ul>\n<li>Invited Lectures<\/li>\n<\/ul>\n<ol>\n<li>\u300cCatalytic Nucleophilic Isocyanation Using Cyanide as an Ambident Reagent\u300d<br \/>\nSNU-HU Joint Young Researchers&#8217; Symposium (\u30bd\u30a6\u30eb\u5927\u5b66\u6821\u30012024\u5e7411\u670827\u65e5)<\/li>\n<li>\u300c\u5e73\u8861\u7684\u306b\u767a\u751f\u3059\u308b\u6709\u6a5f\u30b1\u30a4\u7d20\u30b7\u30a2\u30ce\u30e1\u30bf\u30e9\u30fc\u30c8\u932f\u4f53\u3092\u7528\u3044\u305f\u89e6\u5a92\u7684\u5909\u63db\u53cd\u5fdc\u306e\u958b\u62d3\u300d<br \/>\n\u65e5\u672c\u5316\u5b66\u4f1a\u5317\u6d77\u9053\u652f\u90e8\u652f\u90e8\u5968\u52b1\u8cde\u3000\u53d7\u8cde\u8b1b\u6f14\u4f1a\uff08\u5317\u6d77\u9053\u5927\u5b66\u30012024\u5e742\u670819\u65e5\uff09<\/li>\n<li>\u300cCatalytic Nucleophilic Isocyanation: Selective <em>N<\/em>-Terminus Substitution of Ambident Cyanide\u300d<br \/>\nThe 14th CSE International Summer School &amp; The 11th ALP International Symposium (\u79e9\u7236\u5225\u30012023\u5e748\u670831\u65e5)<\/li>\n<li>\u300cCatalytic Nucleophilic Isocyanation: Selective <em>N<\/em>-Terminus Substitution of Ambident Cyanide\u300d<br \/>\nSICC-11 \uff08\u30b7\u30f3\u30ac\u30dd\u30fc\u30eb\u30012022\u5e7412\u670811\u65e5\uff09<\/li>\n<li>\u300cCatalytic Nucleophilic Isocyanation: Selective <em>N<\/em>-Terminus Substitution of Ambident Cyanide\u300d<br \/>\nICPAP-KK \uff08\u30de\u30ec\u30fc\u30b7\u30a2\u30012022\u5e7411\u670822\u65e5\uff09*Keynote lecture<\/li>\n<li>\u300c\u5b98\u80fd\u6027\u30a4\u30bd\u30cb\u30c8\u30ea\u30eb\u306e\u89e6\u5a92\u7684\u5408\u6210\u6cd5\u300d<br \/>\n2022\u5148\u7aef\u79d1\u5b66\u7814\u7a76\u4f1a\uff08\u5317\u6d77\u9053\u5927\u5b66\u30012022\u5e749\u67083\u65e5\uff09<\/li>\n<li>\u300c\u5927\u6c17\u89e3\u653e\u7cfb\u3067\u306eTsuji\u2013Trost\u30a2\u30ea\u30eb\u4f4d\u7f6e\u63db\u53cd\u5fdc\uff1a\u300e\u8ab0\u3067\u3082\u3067\u304d\u308b\u300f\u6709\u6a5f\u5408\u6210\u3092\u76ee\u6307\u3057\u3066\u300d<br \/>\n2021\u5148\u7aef\u79d1\u5b66\u7814\u7a76\u4f1a \uff08\u30aa\u30f3\u30e9\u30a4\u30f3\u30012021\u5e749\u67084\u65e5)<\/li>\n<li>\u300cCatalytic Isocyanation: Controlling the Ambident Nature of Cyanide\u300d<br \/>\nHokkaido mini-Symposium by Young Generations in Asia\uff08\u5317\u6d77\u9053\u5927\u5b66\u30012019\u5e7411\u670815\u65e5\uff09<\/li>\n<li>\u300c\u30a2\u30f3\u30d3\u30c7\u30f3\u30c8\u306e\u53cd\u5fdc\u6027\u30b3\u30f3\u30c8\u30ed\u30fc\u30eb\uff1a\u89e6\u5a92\u7684\u30a4\u30bd\u30b7\u30a2\u30ce\u5316\u53cd\u5fdc\u306e\u958b\u767a\u300d<br \/>\n\u30d5\u30ed\u30f3\u30c6\u30a3\u30a2\u6750\u6599\u7814\u7a76\u6240\u8b1b\u6f14\u4f1a\u3000\uff08\u6771\u4eac\u5de5\u696d\u5927\u5b66\u30012019\u5e7411\u67088\u65e5\uff09<\/li>\n<li>\u300c\u30a2\u30ea\u30eb\u30a4\u30bd\u30b7\u30a2\u30cb\u30c9\u306e\u4f4d\u7f6e\u9078\u629e\u7684\u5408\u6210\u300d<br \/>\n2018\u5148\u7aef\u79d1\u5b66\u7814\u7a76\u4f1a\uff08\u5927\u962a\u5927\u5b66\u30012018\u5e749\u670822\u65e5\uff09<\/li>\n<li>\u300c\u89e6\u5a92\u7684\u30a4\u30bd\u30b7\u30a2\u30ce\u5316\u53cd\u5fdc\u306e\u958b\u767a\u300d<br \/>\n\u7b2c\uff12\u56de\u3000\u6709\u6a5f\u5408\u6210\u82e5\u624b\u8b1b\u6f14\u4f1a\u3000\uff08\u4eac\u90fd\u5927\u5b66\u30012018\u5e741\u670820\u65e5\uff09<\/li>\n<li>\u300c\u30a2\u30f3\u30d3\u30c7\u30f3\u30c8\u306e\u53cd\u5fdc\u6027\u30b3\u30f3\u30c8\u30ed\u30fc\u30eb\uff1a\u89e6\u5a92\u7684\u30a4\u30bd\u30b7\u30a2\u30ce\u5316\u53cd\u5fdc\u306e\u958b\u767a\u300d<br \/>\n\u82e5\u624b\u7814\u7a76\u8005\u306e\u305f\u3081\u306e\u6709\u6a5f\u5316\u5b66\u672d\u5e4c\u30bb\u30df\u30ca\u30fc\uff08\u5317\u6d77\u9053\u5927\u5b66\u30012017\u5e7411\u670828\u65e5\uff09<\/li>\n<li>\u300c\u6709\u6a5f\u5408\u6210\u306b\u304a\u3051\u308b\u5351\u91d1\u5c5e\u30ca\u30ce\u7c92\u5b50\u306e\u53ef\u80fd\u6027\u300d<br \/>\n\u7b2c\uff15\u56de\u932f\u4f53\u82e5\u624b\u306e\u4f1a\u3000\u5317\u6d77\u9053\u652f\u90e8\u52c9\u5f37\u4f1a\uff08\u5317\u6d77\u9053\u5927\u5b66\u30012016\u5e7411\u670811\u65e5\uff09<\/li>\n<li>Reaxys Prize Club Symposium in Japan 2016\u3000\uff08\u540c\u5fd7\u793e\u5927\u5b66\u30012016\u5e743\u670825\u65e5\uff09<\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n<ul>\n<li>Positionas<\/li>\n<\/ul>\n<ol>\n<li>\u65e5\u672c\u5316\u5b66\u4f1a\u5317\u6d77\u9053\u652f\u90e8\u3000\u4f1a\u8a08\u5e79\u4e8b\uff082022\u5e744\u6708\u301c\u7d99\u7d9a\uff09<\/li>\n<li>\u7b2c\uff13\uff12\u56de\u4e07\u6709\u672d\u5e4c\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\u7d44\u7e54\u59d4\u54e1\u4f1a\uff082020\u5e74\uff09<\/li>\n<li>\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u3000\u5317\u6d77\u9053\u652f\u90e8\u3000\u5eb6\u52d9\u30fb\u5e79\u4e8b (2019\u5e742\u6708\u301c2021\u5e741\u6708)<\/li>\n<li>\u5317\u6d77\u9053\u5927\u5b66\u751f\u5354\u3000\u7dcf\u4ee3\uff08\u5de5\u5b66\uff09 (2018\u5e749\u6708\u301c\u7d99\u7d9a)<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>Papers &#8221;\u00a0 \u00a0 &#8221; T. Yurino,* T. Ishikawa, T. Nakamura, T. Ohkuma* in preparation &#8221;\u00a0 \u00a0 &#8221; T [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":467,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"_links":{"self":[{"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/orgsynth.eng\/Root\/wp-json\/wp\/v2\/pages\/1098"}],"collection":[{"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/orgsynth.eng\/Root\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/orgsynth.eng\/Root\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/orgsynth.eng\/Root\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/orgsynth.eng\/Root\/wp-json\/wp\/v2\/comments?post=1098"}],"version-history":[{"count":54,"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/orgsynth.eng\/Root\/wp-json\/wp\/v2\/pages\/1098\/revisions"}],"predecessor-version":[{"id":2664,"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/orgsynth.eng\/Root\/wp-json\/wp\/v2\/pages\/1098\/revisions\/2664"}],"up":[{"embeddable":true,"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/orgsynth.eng\/Root\/wp-json\/wp\/v2\/pages\/467"}],"wp:attachment":[{"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/orgsynth.eng\/Root\/wp-json\/wp\/v2\/media?parent=1098"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}