{"id":3894,"date":"2024-05-02T13:41:37","date_gmt":"2024-05-02T05:41:37","guid":{"rendered":"\/chemistry\/?p=3894"},"modified":"2024-05-02T15:51:01","modified_gmt":"2024-05-02T07:51:01","slug":"%e6%9e%97%e9%9b%b2%e5%b1%b1","status":"publish","type":"post","link":"\/chemistry\/?p=3894","title":{"rendered":"\u6797\u96f2\u5c71"},"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>\u4ee3\u8868\u6027\u8457\u4f5c<\/strong><\/h4>\n\n\n\n<h5 class=\"wp-block-heading\"><strong>A.\u671f\u520a\u8ad6\u6587<\/strong><\/h5>\n\n\n\n<p>1. Tian-Chyuan Huang,&nbsp;Yun-Shan Lin, Shih-Jue Lin, and Shu-Fan Chu, Diazotization of Methyl 3-Amino-7-isopropyl-2-methoxyazulene-1-carboxylate and its 5-Isopropyl Isomer-A Convenient Synthesis of 1,2-Azulenequinone Derivatives, J. Chin. Chem, Soc.,&nbsp;43, 41-44,(1996).<\/p>\n\n\n\n<p>2. Tian-Chyuan Huang,&nbsp;Yun-Shan Lin, and Tetsuo Nozoe, Synthesis and Polybromination of Azulene[6,5-d]thiazole and It\u2018s 2-Methyl Derivatives, Heterocycles,&nbsp;43, 1049(1996).<\/p>\n\n\n\n<p>3. Tian-Chyuan and&nbsp;Yun-Shan Lin,The Versatile Synthesis of Azulenothiazole Derivatives, J. Chin. Chem. Soc.,&nbsp;43, 365(1996).<\/p>\n\n\n\n<p>4. Tian-Chyuan Huang, Shang-Ya Chiang, and&nbsp;Yun-Shan Lin, The Crystal Structure of Methyl 2-Diazo-3-cyano-4-oxo-2.4-dihydroazulene-1-carboxylate, Formosan Science,&nbsp;49,38-46(1996).<\/p>\n\n\n\n<p>5. Novel Bromination of Diethyl 2-Aminoazulene-1,3-dicarboxylate Tadayoshi Morita, Pai-Feng Tsai, Shin-Min Chen, Fa-Ching Chen, and Yun Shan Lin Sci. Rept Tohoku Univ.&nbsp;78, 9-16(1996).<\/p>\n\n\n\n<p>6. S-J Lin, S-Y Jiang, T-C Huang, P Kao,F. Tsai,H. Takeshita,&nbsp;Y-S Lin,&nbsp;and (the late)T. Nozoe. Photolysis of Diethyl 2-Diazo-6-oxo-2,6-dihydroazulene-1,3-dicarboxylate and Methyl 3-Cyano-2-diazo-6-oxo-2,6-dihydroazulene-1-carboxylate in Tetrahydrofuran. Hetrocycles,&nbsp;45, NO.10 1879-1882(1997).<\/p>\n\n\n\n<p>7. S-J Lin, S-Y Jiang, T-C Huang, C.-S. Dai, F. Tsai,H. Takeshita,&nbsp;Y-S Lin,&nbsp;and (the late)T. Nozoe. A New Convenient Synthesis of 1-2\u2019-Biazulenes by Photolysis of 2-Diazo-1,3-dicyano-2,6-dihydroazulene-6-one with Azulene Derivatives, Bull.Chem. Soc. Jpn.&nbsp;70, NO.12, 3071(1997).<\/p>\n\n\n\n<p>8.&nbsp;Y-S.Lin, S-Y,Jiang,T-C Huang, S-J Lin and Y-L Chow, A New Method for Synthesis of Polyether Bridged Azulenes; Reactions of Conjugated Keto-carbenes Generated from the Corresponding Azulenoquinone Diazides, J.Org, Chem, 1998,&nbsp;63,3364-3370.<\/p>\n\n\n\n<p>9.&nbsp;Y-S Lin, T-C Huang, S-Y Jiang, C-Y Huang, Teruo Kurihara, Hitoshi Takeshita and Tetsuo Nozoe, The Lead(IV) Oxide Mediated Oxidation of Azulen-2-ol to Form 1.1-Coupled Dimers and Hexacyclic Cage-Dimers. Bull. Chem. Soc. Jpn, 2000,&nbsp;73,2793-2803<\/p>\n\n\n\n<p>10. Bo-Cheng Wang, Yun-shan Lin, Jian-Chuang Chang and Pei-Y Wang, Theoretical Studies of Azulene and It&#8217;s Derivatives, Can. J. Chem. 2000, 78, 224-232.<\/p>\n\n\n\n<p>11.&nbsp;Y-S Lin, P-T Kuo, S-T Lin, S-Y Jiang, and C-Y Huang Synthesis and Photolysis of Dibenzyl 2-Diazo-6-oxo-2,6-dihydroazulenequinone-1,3-dicarbonxylate-first Example of Intermolecular C-H Insertion and Intermolecular Electrophilic Substitution on Benzene in the Diazoazulenequinon. Polycycle Aromatic hydrocabms, special issues 2000(Accepted).<\/p>\n\n\n\n<p>12. Ling, Hao-Jan; Chen, Kan-Nan; Lai,Jian-Zei; and Lin, Yun-shan, Uretedione derivative, curable resin composition comprising the same, and process for producing the same. US Patent,6,077,960, Jun.20,2000.<\/p>\n\n\n\n<p>13. Tsoring-Wen Chen, Jen-Yeh, Kan-Nan Chen, and Yun-Shan Lin, Curable system of self-Emulsified Aqueous Epoxy Resin and Its Polymeric Hybrid,US Patent,6,291 55 431, Sep,2001.<\/p>\n\n\n\n<p>14. Bo-Chen Wang, Houng-Wei Wang, I-Chun Lin, Yun-Shan Lin, Yu-Ma Chou and Houn-Lin Chiu, A Semienpirical Study of Carbon Nanotubes with Finite Tubular Length and Various Tubular Diameters. J. Chin. Chem. Soc., 2003, 50,939-945<\/p>\n\n\n\n<p>15.&nbsp;\u6797\u96f2\u5c71\u3001\u4f55\u6771\u82f1\u3001\u9673\u767c\u6e05\u6559\u6388\u7814\u7a76\u7c21\u4ecb-\u5929\u7136\u7269\u5316\u5b78\u4e4b\u7814\u7a76\u3002\u5316\u5b78,\u4e2d\u570b\u5316\u5b78\u6703,\u7b2c\u516d\u5341\u4e00\u5377,\u7b2c\u4e09\u671f,375-384\u9801(2003)<\/p>\n\n\n\n<p>16. Bing-Bing Lin, Tadayoshi Morita, Yun-Shan Lin and Hui-Ling Chen. Facile synthesis of 1-ethoxy-4-cyano-5-ethoxycarbonyl-3H-azulenol[1,2-c]pyran-3-one, a selective 1,5-lipoxygenase inhibitor, Bioorg. Med. Chem. Lett. ,14(2004),63-65<\/p>\n\n\n\n<h5 class=\"wp-block-heading\"><strong>B.\u6703\u8b70\u8ad6\u6587<\/strong><\/h5>\n\n\n\n<p>1.&nbsp;Y-S Lin, S-J Lin, T-C Huang, T. Morita and T. Nozoe, The Formation of Diethenodicyclopenta [ef:kl] heptalene(Diethenoazupyrene)Derivatives, Proceedings of 1996 International. Symposium on Organic Reactions-Sendai,p122(1996),Apr.6-9 1996, Sendai. Japan.<\/p>\n\n\n\n<p>2. T.Nozoe, T-C Huang, M-H Shyr, H. Takeshita, S-Y Chiang and&nbsp;Y-S Lin,&nbsp;Photochemical Reactions of Diazoazulenequinone in Aprotic Solvents, ibid., p148(1996), April. 6-9, 1996, Sendai. Japan.<\/p>\n\n\n\n<p>3. T-C Huang, S-Y Chiang and&nbsp;Y-S Lin, Synthesis of Novel Macrocyclic Polyethers Containing Azulene Unit.&nbsp;\u4e2d\u570b\u5316\u5b78\u6703\u66a8\u9ad8\u96c4\u5206\u6703\u5e74\u6703\uff0c\u516b\u5341\u4e94\u5e74\u5ea6\u624b\u518a\uff0c207\u9801\uff08Dec,7,1996\uff09<\/p>\n\n\n\n<p>4.&nbsp;\u539f\u7530\u5ba3\u4e4b\uff0c\u6c5f\u539f \u5747\uff0c\u5b88\u7530\u5fe0\u7fa9\uff0c\u6797\u96f2\u5c71\uff0c\u6797\u4e16\u667a\uff0c\u91ce\u526f\u9435\u7537\uff0c\u4e8c\u91cf\u9ad4\u5316\u5408\u7269&nbsp;\u5149\u5b78\u5206\u5272&nbsp;\u5713\u4e8c\u8272\u6027&nbsp;\u8209\u52d5\uff0c\u5316\u5b78\u7cfb\u4e03\u5b78\u5354\u6703\u6771\u5317\u5927\u6703\uff0c\u516b\u6236\u5e02\uff0c\u9752\u68ee\u7e23\uff0c\u65e5\u672c\u570b\uff0c1996\u5e7410\u67082~3\u65e5.<\/p>\n\n\n\n<p>5.\u6797\u4e16\u667a\uff0c\u6c5f\u9078\u96c5\uff0c\u9ec3\u6dfb\u9293\uff0c\u6234\u653f\u8ce2\uff0c\u8521\u767e\u8c50\uff0c\u6797\u96f2\u5c71\uff0cH. Takeshita, T. Nozoe A New Convenient Synthesis of 1,2\u2019-Biazulene by Photolysis of 2-Diazo-1, 3-dicyanoazulene-6-(2H)-one with Azulene Derivatives.&nbsp;\u4e2d\u570b\u5316\u5b78\u670386\u5e74\u5e74\u6703\u624b\u518a\uff0c274\u9801(1997)\u65b0\u7af9\u5de5\u696d\u6280\u8853\u7814\u7a76\u9662.<\/p>\n\n\n\n<p>6.&nbsp;Y-S Lin&nbsp;and S-Y Jiang, An Improved Synthesis of 2-Arylazulene Derivatives, The 9<sup>th<\/sup>&nbsp;International Symposium of Novel Aromatic Compounds (ISNA-9), 2nd-7th August, 1998, Theatre II, Hong Kong Convention Exhibition center, Wanchai, Hong Kong.<\/p>\n\n\n\n<p>7.&nbsp;Y-S Lin, P-T Kuo, S-T Lin, S-Y Jiang, and C-Y Huang Synthesis and Photolysis of Dibenzyl 2-Diazo-6-oxo-2,6-dihydroazulenequinone-1,3-dicarbonxylate-first Example of Intermolecular C-H Insertion and Intermolecular Electrophilic Substitution on Benzene in the Diazoazulenequinon. The 7<sup>th<\/sup>. International Symposium on Polycyclic Aromatic compounds. Oct. 25-29, 1999, Convention center, Bordeaux, France, Abstr. p99.<\/p>\n\n\n\n<p>8.&nbsp;Y-S Lin, Hsing-Lin Jiang, Shuan-Ya Jiang, and Chien-Yi Huang, Synthesis of 1-Diazo-8-xix-1,8-dihydroazulenequinone and It&#8217;s Potolysis in various solvents. 8th Asian Chemical congress, Nov. 21-24,1999. International Convention Center, Taipei, Taiwan, Abstr. p549.<\/p>\n<\/div>\n<\/div>\n\n\n\n<div style=\"height:10px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":7,"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\/3894"}],"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\/7"}],"replies":[{"embeddable":true,"href":"\/chemistry\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=3894"}],"version-history":[{"count":2,"href":"\/chemistry\/index.php?rest_route=\/wp\/v2\/posts\/3894\/revisions"}],"predecessor-version":[{"id":3939,"href":"\/chemistry\/index.php?rest_route=\/wp\/v2\/posts\/3894\/revisions\/3939"}],"wp:attachment":[{"href":"\/chemistry\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=3894"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"\/chemistry\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=3894"},{"taxonomy":"post_tag","embeddable":true,"href":"\/chemistry\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=3894"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}