{"id":8,"date":"2013-04-12T15:17:20","date_gmt":"2013-04-12T07:17:20","guid":{"rendered":"http:\/\/wp.kmu.edu.tw\/enchwa\/?page_id=8"},"modified":"2013-04-12T15:17:33","modified_gmt":"2013-04-12T07:17:33","slug":"%e7%a0%94%e7%a9%b6%e8%91%97%e4%bd%9c","status":"publish","type":"page","link":"https:\/\/wp.kmu.edu.tw\/enchwa\/%e7%a0%94%e7%a9%b6%e8%91%97%e4%bd%9c\/","title":{"rendered":"\u7814\u7a76\u8457\u4f5c"},"content":{"rendered":"<p><b>Paper published<\/b> (2012-2009)<\/p>\n<ol>\n<li>Chen, Po-Yuan; Huang, Keng-Shiang; Tsai, Chin-Chuan; Wang, Tzu-Pin; <b>Wang, Eng-Chi<\/b><b>*<\/b> \u201c<a href=\"https:\/\/scifinder.cas.org\/scifinder\/references\/answers\/F70A04BDX86F35092X694B5474262233CCBF:F70B5756X86F35092X4BF7B73D4C8477AF79\/1.html?nav=eNpVkLEvQ0Ecx39e04jogEVEiMEgJPeEtq9Cgqpq4-VVFBFLc20v7eO9d8_dtdpFGDBYDMpiMNjYiT9BYhQWidhZJSb3WiK96ZLf5z73_X1vPsAvoAULGIxro9GQFgqvR8Lx8dDoxNh6MBrXotp4LDgXCWrabFybkGiWM-jcxGWMLOwUUNIRpEBY1_vl1df-UUSBliT4y9gqkQqDjn_OKNlZwg5van3tp2_HCkDFBQCfFBYF9M6uriRSy5mksTZvrMiLkcosLKdWl5LGgoA203YpE9LAt2EXfPIdCFAYbU4SpdQi2HkcYHtPF9-fMsnGXxLX4zmX_AhlBZTDHFGewwxxwsqEoTy1semgHLVt6qC0_CztktzUyfVl3_nbgwKKDgG7mmJ508HWIqkKGNKlSJUitS5SGyK1IVIbIlWSkzq02lXPyAX06F5atSRMS9VNZ4vkE5gX00RMVlxXhuuuL-ONUdP4xXreqL0O93ut_a1cp37n97GD2tndbdDntboTkPV0TM9A_VR-ADVVne8&amp;key=caplus_2012:1288376&amp;title=Pd(II)-Mediated%20Cyclization%20of%20o-Allylbenzaldehydes%20in%20Water:%20A%20Novel%20Synthesis%20of%20Isocoumarins&amp;launchSrc=reflist&amp;p=1\">Pd(II)-Mediated Cyclization of o-Allylbenzaldehydes in Water: A Novel Synthesis of Isocoumarins\u201d <\/a><\/li>\n<\/ol>\n<p><i>Org<\/i><i>.<\/i><i> Lett<\/i>. <b>2012<\/b>, <i>14<\/i>, 4930-4933.<\/p>\n<ol>\n<li>Chen, Hsing-Ming; Chen, Po-Yuan; Wang, Chih-Feng; Tsai, Jui-Chi; <b>Wang, Eng-Chi<\/b><b>*<\/b> \u201c<a href=\"https:\/\/scifinder.cas.org\/scifinder\/references\/answers\/F70A04BDX86F35092X694B5474262233CCBF:F70B5756X86F35092X4BF7B73D4C8477AF79\/2.html?nav=eNpVkLEvQ0Ecx39e04jogEVEiMEgJPeEtq9Cgqpq4-VVFBFLc20v7eO9d8_dtdpFGDBYDMpiMNjYiT9BYhQWidhZJSb3WiK96ZLf5z73_X1vPsAvoAULGIxro9GQFgqvR8Lx8dDoxNh6MBrXotp4LDgXCWrabFybkGiWM-jcxGWMLOwUUNIRpEBY1_vl1df-UUSBliT4y9gqkQqDjn_OKNlZwg5van3tp2_HCkDFBQCfFBYF9M6uriRSy5mksTZvrMiLkcosLKdWl5LGgoA203YpE9LAt2EXfPIdCFAYbU4SpdQi2HkcYHtPF9-fMsnGXxLX4zmX_AhlBZTDHFGewwxxwsqEoTy1semgHLVt6qC0_CztktzUyfVl3_nbgwKKDgG7mmJ508HWIqkKGNKlSJUitS5SGyK1IVIbIlWSkzq02lXPyAX06F5atSRMS9VNZ4vkE5gX00RMVlxXhuuuL-ONUdP4xXreqL0O93ut_a1cp37n97GD2tndbdDntboTkPV0TM9A_VR-ADVVne8&amp;key=caplus_2012:1041949&amp;title=An%20improved%20method%20for%20the%20conversion%20of%20oxiranes%20to%20thiiranes%20and%20the%20discrimination%20of%20their%20base%20peaks%20in%20EI-MS&amp;launchSrc=reflist&amp;p=1\">An improved method for the conversion of oxiranes to thiiranes and the discrimination of their base peaks in <\/a><\/li>\n<\/ol>\n<p><a href=\"https:\/\/scifinder.cas.org\/scifinder\/references\/answers\/F70A04BDX86F35092X694B5474262233CCBF:F70B5756X86F35092X4BF7B73D4C8477AF79\/2.html?nav=eNpVkLEvQ0Ecx39e04jogEVEiMEgJPeEtq9Cgqpq4-VVFBFLc20v7eO9d8_dtdpFGDBYDMpiMNjYiT9BYhQWidhZJSb3WiK96ZLf5z73_X1vPsAvoAULGIxro9GQFgqvR8Lx8dDoxNh6MBrXotp4LDgXCWrabFybkGiWM-jcxGWMLOwUUNIRpEBY1_vl1df-UUSBliT4y9gqkQqDjn_OKNlZwg5van3tp2_HCkDFBQCfFBYF9M6uriRSy5mksTZvrMiLkcosLKdWl5LGgoA203YpE9LAt2EXfPIdCFAYbU4SpdQi2HkcYHtPF9-fMsnGXxLX4zmX_AhlBZTDHFGewwxxwsqEoTy1semgHLVt6qC0_CztktzUyfVl3_nbgwKKDgG7mmJ508HWIqkKGNKlSJUitS5SGyK1IVIbIlWSkzq02lXPyAX06F5atSRMS9VNZ4vkE5gX00RMVlxXhuuuL-ONUdP4xXreqL0O93ut_a1cp37n97GD2tndbdDntboTkPV0TM9A_VR-ADVVne8&amp;key=caplus_2012:1041949&amp;title=An%20improved%20method%20for%20the%20conversion%20of%20oxiranes%20to%20thiiranes%20and%20the%20discrimination%20of%20their%20base%20peaks%20in%20EI-MS&amp;launchSrc=reflist&amp;p=1\">EI-MS<b> <\/b><\/a><b> <\/b> <i>ARKIVOC<\/i> (Gainesville, FL, United States), <b>2012<\/b>, <i>8<\/i>, 157-168.<\/p>\n<ol>\n<li><b>Wang, Eng-Chi<\/b><b>*<\/b>; Tsai, Jui-Chi; Li, Sie-Rong; Chen, Po-Yuan \u201c<a href=\"https:\/\/scifinder.cas.org\/scifinder\/references\/answers\/F70A04BDX86F35092X694B5474262233CCBF:F70B5756X86F35092X4BF7B73D4C8477AF79\/3.html?nav=eNpVkLEvQ0Ecx39e04jogEVEiMEgJPeEtq9Cgqpq4-VVFBFLc20v7eO9d8_dtdpFGDBYDMpiMNjYiT9BYhQWidhZJSb3WiK96ZLf5z73_X1vPsAvoAULGIxro9GQFgqvR8Lx8dDoxNh6MBrXotp4LDgXCWrabFybkGiWM-jcxGWMLOwUUNIRpEBY1_vl1df-UUSBliT4y9gqkQqDjn_OKNlZwg5van3tp2_HCkDFBQCfFBYF9M6uriRSy5mksTZvrMiLkcosLKdWl5LGgoA203YpE9LAt2EXfPIdCFAYbU4SpdQi2HkcYHtPF9-fMsnGXxLX4zmX_AhlBZTDHFGewwxxwsqEoTy1semgHLVt6qC0_CztktzUyfVl3_nbgwKKDgG7mmJ508HWIqkKGNKlSJUitS5SGyK1IVIbIlWSkzq02lXPyAX06F5atSRMS9VNZ4vkE5gX00RMVlxXhuuuL-ONUdP4xXreqL0O93ut_a1cp37n97GD2tndbdDntboTkPV0TM9A_VR-ADVVne8&amp;key=caplus_2012:539008&amp;title=Method%20for%20preparing%20coumarin%20and%20chromene%20compounds&amp;launchSrc=reflist&amp;p=1\">Method for preparing coumarin and chromene compounds <\/a>\u201c U.S. Pat. Appl. Publ. <b>2012<\/b>, US 20120088923 A1 20120412<\/li>\n<li>Chen, Po-Yuan; Chen, Hsing-Ming; Chiang, Michael Y.; Wang, You-Feng; Li, Sie-Rong; Wang, Tzu-Pin; <b>Wang, Eng-Chi<\/b><b>* \u201c<\/b>A novel and chemoselective synthesis of substituted<\/li>\n<\/ol>\n<p>3,4-dihydroisoquinolin-1(2H)-ones from o-oxiranylmethylbenzonitrile intermediates and TBAB\/NaCN<b>\u201d<\/b> <i>Tetrahedron<\/i><b> 2012<\/b>, <i>68<\/i>, 3030-3036.<\/p>\n<ol>\n<li>Wang, Tzu-Pin*; Su, Yu-Chih; Chen, Yi; Liou, Yi-Ming; Lin, Kun-Liang; <b>Wang, Eng-Chi<\/b>; Hwang, Long-Chih; Wang, Yun-Ming; Chen, Yen-Hsu \u201c<\/li>\n<\/ol>\n<p><a href=\"https:\/\/scifinder.cas.org\/scifinder\/references\/answers\/F70A04BDX86F35092X694B5474262233CCBF:F70B5756X86F35092X4BF7B73D4C8477AF79\/6.html?nav=eNpVkLEvQ0Ecx39e04jogEVEiMEgJPeEtq9Cgqpq4-VVFBFLc20v7eO9d8_dtdpFGDBYDMpiMNjYiT9BYhQWidhZJSb3WiK96ZLf5z73_X1vPsAvoAULGIxro9GQFgqvR8Lx8dDoxNh6MBrXotp4LDgXCWrabFybkGiWM-jcxGWMLOwUUNIRpEBY1_vl1df-UUSBliT4y9gqkQqDjn_OKNlZwg5van3tp2_HCkDFBQCfFBYF9M6uriRSy5mksTZvrMiLkcosLKdWl5LGgoA203YpE9LAt2EXfPIdCFAYbU4SpdQi2HkcYHtPF9-fMsnGXxLX4zmX_AhlBZTDHFGewwxxwsqEoTy1semgHLVt6qC0_CztktzUyfVl3_nbgwKKDgG7mmJ508HWIqkKGNKlSJUitS5SGyK1IVIbIlWSkzq02lXPyAX06F5atSRMS9VNZ4vkE5gX00RMVlxXhuuuL-ONUdP4xXreqL0O93ut_a1cp37n97GD2tndbdDntboTkPV0TM9A_VR-ADVVne8&amp;key=caplus_2011:1632846&amp;title=In%20Vitro%20Selection%20and%20Characterization%20of%20a%20Novel%20Zn(II)-Dependent%20Phosphorothiolate%20Thiolesterase%20Ribozyme&amp;launchSrc=reflist&amp;p=1\">In Vitro Selection and Characterization of a Novel \u00a0\u00a0\u00a0 Zn(II)-Dependent Phosphorothiolate Thiolesterase Ribozyme <\/a>\u201c <i>Biochemistry <\/i><b>2012<\/b>, <i>51<\/i>, 496-510.<\/p>\n<ol>\n<li>Wang, Tzu-Pin*; Chang, Li-Lin; Chang, Sheng-Nan; <b>Wang, Eng-Chi<\/b>; Hwang, Long-Chih; Chen, Yen- Hsu; Wang, Yun-Ming \u201c<a href=\"https:\/\/scifinder.cas.org\/scifinder\/references\/answers\/F70A04BDX86F35092X694B5474262233CCBF:F70B5756X86F35092X4BF7B73D4C8477AF79\/5.html?nav=eNpVkLEvQ0Ecx39e04jogEVEiMEgJPeEtq9Cgqpq4-VVFBFLc20v7eO9d8_dtdpFGDBYDMpiMNjYiT9BYhQWidhZJSb3WiK96ZLf5z73_X1vPsAvoAULGIxro9GQFgqvR8Lx8dDoxNh6MBrXotp4LDgXCWrabFybkGiWM-jcxGWMLOwUUNIRpEBY1_vl1df-UUSBliT4y9gqkQqDjn_OKNlZwg5van3tp2_HCkDFBQCfFBYF9M6uriRSy5mksTZvrMiLkcosLKdWl5LGgoA203YpE9LAt2EXfPIdCFAYbU4SpdQi2HkcYHtPF9-fMsnGXxLX4zmX_AhlBZTDHFGewwxxwsqEoTy1semgHLVt6qC0_CztktzUyfVl3_nbgwKKDgG7mmJ508HWIqkKGNKlSJUitS5SGyK1IVIbIlWSkzq02lXPyAX06F5atSRMS9VNZ4vkE5gX00RMVlxXhuuuL-ONUdP4xXreqL0O93ut_a1cp37n97GD2tndbdDntboTkPV0TM9A_VR-ADVVne8&amp;key=caplus_2012:155858&amp;title=Successful%20preparation%20and%20characterization%20of%20biotechnological%20grade%20agarose%20from%20indigenous%20Gelidium%20amansii%20of%20Taiwan&amp;launchSrc=reflist&amp;p=1\">Successful preparation and characterization of biotechnological grade <\/a><\/li>\n<\/ol>\n<p><a href=\"https:\/\/scifinder.cas.org\/scifinder\/references\/answers\/F70A04BDX86F35092X694B5474262233CCBF:F70B5756X86F35092X4BF7B73D4C8477AF79\/5.html?nav=eNpVkLEvQ0Ecx39e04jogEVEiMEgJPeEtq9Cgqpq4-VVFBFLc20v7eO9d8_dtdpFGDBYDMpiMNjYiT9BYhQWidhZJSb3WiK96ZLf5z73_X1vPsAvoAULGIxro9GQFgqvR8Lx8dDoxNh6MBrXotp4LDgXCWrabFybkGiWM-jcxGWMLOwUUNIRpEBY1_vl1df-UUSBliT4y9gqkQqDjn_OKNlZwg5van3tp2_HCkDFBQCfFBYF9M6uriRSy5mksTZvrMiLkcosLKdWl5LGgoA203YpE9LAt2EXfPIdCFAYbU4SpdQi2HkcYHtPF9-fMsnGXxLX4zmX_AhlBZTDHFGewwxxwsqEoTy1semgHLVt6qC0_CztktzUyfVl3_nbgwKKDgG7mmJ508HWIqkKGNKlSJUitS5SGyK1IVIbIlWSkzq02lXPyAX06F5atSRMS9VNZ4vkE5gX00RMVlxXhuuuL-ONUdP4xXreqL0O93ut_a1cp37n97GD2tndbdDntboTkPV0TM9A_VR-ADVVne8&amp;key=caplus_2012:155858&amp;title=Successful%20preparation%20and%20characterization%20of%20biotechnological%20grade%20agarose%20from%20indigenous%20Gelidium%20amansii%20of%20Taiwan&amp;launchSrc=reflist&amp;p=1\">agarose from indigenous Gelidium amansii of Taiwan\u201d <\/a>Process Biochemistry (Oxford, United Kingdom) <b>2012<\/b>, <i>47<\/i>, 550-554.<\/p>\n<ol>\n<li>Chen, Po-Yuan; Wang, Tzu-Pin; Huang, Keng-Shiang; Kao, Chai-Lin; Tsai, Jui-Chi; <b>Wang, Eng-Chi<\/b><b>*<\/b><\/li>\n<\/ol>\n<p>\u201ctert-BuOK-mediated carbanion-yne intramolecular cyclization: synthesis of 2-substituted 3-benzyl-Benzofurans\u201d <i>Tetrahedron<\/i> <b>2011<\/b>, <i>67<\/i>, 9291-9297.<\/p>\n<ol>\n<li>Chen, Po-Yuan; Wang, Tzu-Pin; Chiang, Michael Y.; Huang, Keng-Shian; Tzeng, Cherng-Chyi; Chen, Yi-Long; <b>Wang, Eng-Chi*<\/b> \u201cenvironmentally benign syntheses of flavanones<b>\u201d <\/b><i>Tetrahedron<\/i><\/li>\n<\/ol>\n<p><b>2011<\/b>, <i>67<\/i>, 4155-4160.<\/p>\n<ol>\n<li>Chen, Liang-Yeu; Li, Sie-Rong; Chen, Po-Yuan; Chang, Ho-Chiang; Wang, Tzu-Pin; Tsai, Ian-Lih; <b>Wang, Eng-Chi* <\/b>\u201c<a href=\"https:\/\/scifinder.cas.org\/scifinder\/references\/answers\/F77A2440X86F35098X24CFFB751356BB3F19:F77AE9FEX86F35098X3CE5B7C95218ABF116\/12.html?nav=eNpVkLEvQ0Ecx39eIyI6lEVEKgaDkNxTVNtUQlttNV5eRRGxyGkv7eO9d8_dtdpFGDBYDMpiMNjYiT9BYhQWidhZJSb3WiJuuuT3uc99f9_rd2gV0IIFDKRCoVgykkquhCdSY8GRSHhlLJEMxkOJSHA0EI7FU4HAhETXOYPODVzByMR2EWVsQYqEdb1dXH7uHYYVaMlAawWbZVJl4Pvj9LK1TtjBdd3fcfJ6pABUHQDwSGFJQG9saXE2u7CW0ZeT-qK86Nm19EJ2aT6jpwW0G5ZDmZAGvgU74JHvQIDC6P8kcUpNgu2Hfrb7eP71IZOs_iZxXJ5zyQ9TVkR5zBHlecwQJ6xCGCpQCxs2ylPLojbKyc9yDslPHl9d-M9e7xVQNPBatSwrGDY250hNwKAmRaoUqQ2R2hSpTZHaFKmSjGrQZtVcIxfQo7lp1bIwTFUz7E1SmMW8lCMiWnUcGa67sYw7Rv_Gz-bTav1lqM9t7XflBvUzv5vZr5_e3ox73Fa3vbIe39Q0NE71G4Gxnhg&amp;key=caplus_2010:1198340&amp;title=2,3-dichloro-5,6-dicyanobenzoquinone%20(DDQ)%20mediated%20oxidation-dehydrogenation%20of%202-aroyl-3,4-dihydro-2H-benzopyrans:%20synthesis%20of%202-aroylbenzopyran-4-ones&amp;launchSrc=reflist&amp;p=1\">2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) mediated\u00a0 <\/a><\/li>\n<\/ol>\n<p><a href=\"https:\/\/scifinder.cas.org\/scifinder\/references\/answers\/F77A2440X86F35098X24CFFB751356BB3F19:F77AE9FEX86F35098X3CE5B7C95218ABF116\/12.html?nav=eNpVkLEvQ0Ecx39eIyI6lEVEKgaDkNxTVNtUQlttNV5eRRGxyGkv7eO9d8_dtdpFGDBYDMpiMNjYiT9BYhQWidhZJSb3WiJuuuT3uc99f9_rd2gV0IIFDKRCoVgykkquhCdSY8GRSHhlLJEMxkOJSHA0EI7FU4HAhETXOYPODVzByMR2EWVsQYqEdb1dXH7uHYYVaMlAawWbZVJl4Pvj9LK1TtjBdd3fcfJ6pABUHQDwSGFJQG9saXE2u7CW0ZeT-qK86Nm19EJ2aT6jpwW0G5ZDmZAGvgU74JHvQIDC6P8kcUpNgu2Hfrb7eP71IZOs_iZxXJ5zyQ9TVkR5zBHlecwQJ6xCGCpQCxs2ylPLojbKyc9yDslPHl9d-M9e7xVQNPBatSwrGDY250hNwKAmRaoUqQ2R2hSpTZHaFKmSjGrQZtVcIxfQo7lp1bIwTFUz7E1SmMW8lCMiWnUcGa67sYw7Rv_Gz-bTav1lqM9t7XflBvUzv5vZr5_e3ox73Fa3vbIe39Q0NE71G4Gxnhg&amp;key=caplus_2010:1198340&amp;title=2,3-dichloro-5,6-dicyanobenzoquinone%20(DDQ)%20mediated%20oxidation-dehydrogenation%20of%202-aroyl-3,4-dihydro-2H-benzopyrans:%20synthesis%20of%202-aroylbenzopyran-4-ones&amp;launchSrc=reflist&amp;p=1\">oxidation-dehydrogenation of 2-aroyl-3,4-dihydro-2H-benzopyrans: synthesis of 2-aroylbenzopyran-4-ones\u201d<b> <\/b><\/a>ARKIVOC (Gainesville, FL, United States) <b>2010,<\/b> <i>11<\/i>, 64-76.<\/p>\n<h2>10.\u00a0\u00a0\u00a0\u00a0 Wang, Tzu-Pin*; Chiou, Yi-Jang; Chen, Yi; Wang, Eng-Chi; Hwang, Long-Chih; Chen, Bing-Hung; Chen, Yen-Hsu; Ko, Chun-Han \u201c<a href=\"https:\/\/scifinder.cas.org\/scifinder\/references\/answers\/F77A2440X86F35098X24CFFB751356BB3F19:F77AE9FEX86F35098X3CE5B7C95218ABF116\/13.html?nav=eNpVkLEvQ0Ecx39eIyI6lEVEKgaDkNxTVNtUQlttNV5eRRGxyGkv7eO9d8_dtdpFGDBYDMpiMNjYiT9BYhQWidhZJSb3WiJuuuT3uc99f9_rd2gV0IIFDKRCoVgykkquhCdSY8GRSHhlLJEMxkOJSHA0EI7FU4HAhETXOYPODVzByMR2EWVsQYqEdb1dXH7uHYYVaMlAawWbZVJl4Pvj9LK1TtjBdd3fcfJ6pABUHQDwSGFJQG9saXE2u7CW0ZeT-qK86Nm19EJ2aT6jpwW0G5ZDmZAGvgU74JHvQIDC6P8kcUpNgu2Hfrb7eP71IZOs_iZxXJ5zyQ9TVkR5zBHlecwQJ6xCGCpQCxs2ylPLojbKyc9yDslPHl9d-M9e7xVQNPBatSwrGDY250hNwKAmRaoUqQ2R2hSpTZHaFKmSjGrQZtVcIxfQo7lp1bIwTFUz7E1SmMW8lCMiWnUcGa67sYw7Rv_Gz-bTav1lqM9t7XflBvUzv5vZr5_e3ox73Fa3vbIe39Q0NE71G4Gxnhg&amp;key=caplus_2010:980317&amp;title=Versatile%20Phosphoramidation%20Reactions%20for%20Nucleic%20Acid%20Conjugations%20with%20Peptides,%20Proteins,%20Chromophores,%20and%20Biotin%20Derivatives&amp;launchSrc=reflist&amp;p=1\">Versatile Phosphoramidation Reactions for Nucleic Acid \u00a0\u00a0\u00a0 <\/a><\/h2>\n<h2><a href=\"https:\/\/scifinder.cas.org\/scifinder\/references\/answers\/F77A2440X86F35098X24CFFB751356BB3F19:F77AE9FEX86F35098X3CE5B7C95218ABF116\/13.html?nav=eNpVkLEvQ0Ecx39eIyI6lEVEKgaDkNxTVNtUQlttNV5eRRGxyGkv7eO9d8_dtdpFGDBYDMpiMNjYiT9BYhQWidhZJSb3WiJuuuT3uc99f9_rd2gV0IIFDKRCoVgykkquhCdSY8GRSHhlLJEMxkOJSHA0EI7FU4HAhETXOYPODVzByMR2EWVsQYqEdb1dXH7uHYYVaMlAawWbZVJl4Pvj9LK1TtjBdd3fcfJ6pABUHQDwSGFJQG9saXE2u7CW0ZeT-qK86Nm19EJ2aT6jpwW0G5ZDmZAGvgU74JHvQIDC6P8kcUpNgu2Hfrb7eP71IZOs_iZxXJ5zyQ9TVkR5zBHlecwQJ6xCGCpQCxs2ylPLojbKyc9yDslPHl9d-M9e7xVQNPBatSwrGDY250hNwKAmRaoUqQ2R2hSpTZHaFKmSjGrQZtVcIxfQo7lp1bIwTFUz7E1SmMW8lCMiWnUcGa67sYw7Rv_Gz-bTav1lqM9t7XflBvUzv5vZr5_e3ox73Fa3vbIe39Q0NE71G4Gxnhg&amp;key=caplus_2010:980317&amp;title=Versatile%20Phosphoramidation%20Reactions%20for%20Nucleic%20Acid%20Conjugations%20with%20Peptides,%20Proteins,%20Chromophores,%20and%20Biotin%20Derivatives&amp;launchSrc=reflist&amp;p=1\">Conjugations with Peptides, Proteins, Chromophores, and Biotin Derivatives\u201d <\/a> <i>Bioconjugate<\/i><i> Chemistry<\/i> 2010, <i>21<\/i>, 1642-1655.<\/h2>\n<ol>\n<li><b>Wang, E.-C<\/b>.; Li, S.-R.\u00a0 \u201c Intermediate compounds and processes for the preparation of 7-benzyloxy-3-(4-methoxyphenyl)-2H-1-benzopyran\u201d<b>.<\/b> <b>U.S. Pat. Appl. Publ.<\/b><i> <\/i> (<b>2010<\/b>), 6pp.\u00a0 CODEN:<\/li>\n<\/ol>\n<p>USXXCO US 2010298582 A1 20101125 AN 2010:1465099.<\/p>\n<ol>\n<li>Wang, Eng-Chi; Li, Sie-Rong. \u201cProcesses for preparing isoflavonoids using 7-benzyloxy-3-(4-methoxyphenyl)-2H-1-benzopyran as a starting material\u201d<i>.<\/i><i> <\/i><b>U.S. Pat. Appl. Publ.<\/b><i> <\/i> (<b>2010<\/b>), 11pp.\u00a0 CODEN: USXXCO US 2010298581 A1 20101125 AN 2010:1465096.<\/li>\n<li>Chen, L.-Y.; Li, S.-R.; Chen, P.-Y.; Chang, H.-C.; Wang, T.-P.; Tsai, I.-L.; <b>Wang, E.-C.<\/b>*\u00a0 <i>ARKIVOC<\/i> (Gainesville, FL, United States)\u00a0 <b>2010<\/b>,\u00a0 <i>11<\/i>,\u00a0 64-76.<\/li>\n<li>Wang, T.-P.; Chiou, Y.-J.; Chen, Y.; <b>Wang, E.-C<\/b>.; Hwang, L.-C.; Chen, B.-H.; Chen, Y.-H.; Ko, C.-H. <i>Bioconjugate<\/i><i> Chem<\/i>. <b>2010<\/b>, <i>21<\/i>, 1642-1655.<\/li>\n<li>Tsai, J.-C.; Li, S-R.; Chiang, Michael Y.; Chen, L.-Y.; Chen, P. Y.; Lo, Y.-F.; Wang, C.-H.; Lin, C.-N.<b> Wang, E.-C.*<\/b> \u201cA novel synthesis of 3-alkoxymethylcoumarins from 3-cyanochromenes <i>via <\/i>2-phenylimino-3-alkoxymethylchromenes intermediates\u201d <i>J. Org. Chem. <\/i><b>2009<\/b><i>, 74, <\/i>8789-8801<i>.<\/i><\/li>\n<li>Li, S-R.; Shu, C.-J.; Chen, L.-Y.; Chen, H.-M.; Chen, P. Y.;<b>Wang<\/b><b>, E.-C.<sup>*<\/sup> <\/b>\u201cSynthesis of substituted 2-aroyl-3-methylchromen-4-ones from isovanillin <i>via <\/i>2-aroyl-3- methylchroman intermediates\u201d <i>Tetrahedron <\/i><b>2009<\/b>, <i>65<\/i>, 8702-8707.<\/li>\n<li>Chen, L.-Y.; Li, S-R.; Chen, P. Y.; Tsai, I.-L.; Hsu, C. L.; Lin, H. P.; Wang, T. P.;<b>Wang<\/b><b>, E.-C<\/b>.* \u201cA novel carbanion-olefin intramolecular cyclization: synthesis of substituted 2-aroyl-1-dihydrobenzopyrans from salicylaldehydes\u201d <i>Tetrahedron Lett<\/i>.<b>2009<\/b>, <i>50<\/i>, 5748-575<\/li>\n<li>Li, S-R.; Chen, P. Y.; Chen, P. Y.; Lo, Y.-F.; Tsai, I.-L.; <b>Wang, E.-C<\/b>.* \u201cSynthesis of haginin E, equol, daidzein, and formononetin from resorcinol <i>via<\/i> isoflavene intermediates\u201d <i>Tetrahedron<\/i> <i>Lett<\/i>. <b>2009<\/b>, <i>50<\/i>, 2121-2123.<\/li>\n<li>Lin, Y. S.; Huang, K. S.;* Yang, C. H.;* <b>Wang, E.-C<\/b>.* Jhong, J. Y.; Hsu, C. J.; Kuo, C. Y. \u201cPrecise control of chitosan microparticles using a double T-junction microchannel chip: facile separation of satellite drops\u201d <i>LAB CHIP<\/i>, <b>2009, <\/b><i>9<\/i>, 145-150.<\/li>\n<li>Tsai, J.-C.; Li, S-R.; Chen, L.-Y.; Chen, P. Y.; Jhong, J. Y.; Shu, C.-J.; Lo, Y.-F.; Lin, C.-N.<b> Wang, E.-C<\/b>.* \u201cSynthesis of 3-aryl-2,5-dihydro-1-benzoxepines from Phenol <i>via<\/i> ring-closing metathesis\u201d<i> J. Chin. Chem. Soc.<\/i> <b>2008<\/b>, <i>55<\/i>, 1317-1321.<\/li>\n<li>Tsai, J.-C.; Li, S-R.; Chen, L.-Y.; Chen, P. Y.;\u00a0 Hsu, Sodio C.-N.; Lin, C.-N.; <b>Wang, E.-C.<\/b>.* \u201cSynthesis of substituted 2,5-dihydro-1-naphthoxepines from 1-naphthol via ring-closing metathesis<b>\u201d<\/b> <i>ARKIVOC<\/i> (Gainesville, FL, United States) <b>2008<\/b>, <i>12<\/i>, 205-217.<\/li>\n<li>Lin, G.-T.; Tseng, H.-F.; Chang, C.-K.; Chuang, L.-Y.; Liu, C.-S.; Yang, C.-H.; Tu, C.-J.; <b>Wang, E.-C.<\/b>; Tan, H.-F.; Chang, C.-C.; Wen, C.-H.; Chen, H.-C.; Chang, H.-W. <b> \u201c<\/b>SNP combinations in<b> <\/b>chromosome-wide genes are associated with bone mineral density in Taiwanese women\u201d. <i>Chin. J. Physiol<\/i>. <b>2008<\/b>, <i>51<\/i>, 32-41.<\/li>\n<li>Li, S-R.; Chen, H.-M.; Chen, P. Y.;\u00a0 Tsai, J.-C.; Chen, L.-Y.; <b>Wang, E.-C.<\/b>;* Huang, Y.-T.; Wei, Y.-C.; Lu, P.-J.. \u201cSynthesis and evaluation of the cytotoxicities of neoflavenes<b>.\u201d<\/b> <i>J. Chin. Chem. Soc. <\/i><b>2008<\/b>, <i>55<\/i>, 923-932.<\/li>\n<li>Li, S-R.; Chen, H.-M.; Chen, L.-Y.; Tsai, J.-C.; Chen, P. Y.; Hsu, Sodio C.-N.; <b>Wang, E.-C.<\/b>.* \u201cSynthesis of 1-benzoxepin-5-ones (ols) from salicylaldehydes via ring-closing metathesis\u201d <i>ARKIVOC<\/i> (Gainesville, FL, United States) <b>2008<\/b>, <i>2<\/i>, 172-182.<\/li>\n<li>Li, S-R.; Chen, L.-Y.; Tsai, J.-C.; Tzeng, J. Y.; Tsai, I. L.; <b>Wang, E.-C.*<\/b> \u201cNew syntheses of dalbergichromene and dalbergin from vanillin via neoflavene intermediate.\u201d <i>Tetrahedron Lett.<\/i> <b>2007<\/b>, <i>48<\/i>, 2139-2141.<\/li>\n<li><b>Wang, E.-C.; <\/b>Wu, C. H. ; Chien, S. C. ; Chiang, W. C.;\u00a0 Kuo, Y. H.* \u201cAn efficient and chemoselective deprotection of aryl- and styrenyldithioketals (acetals).\u201d<i> Tetrahedron Lett.<\/i> <b>2007<\/b>, <i>48<\/i>, 7706-7708.<\/li>\n<li>Li, S-R.; Chen, L.-Y.; Tsai, J.-C.; Tzeng, J. Y.; Tsai, I. L.; <b>Wang, E.-C.*<\/b> \u201cNew syntheses of dalbergichromene and dalbergin from vanillin via neoflavene intermediate.\u201d <i>Tetrahedron Lett.<\/i> <b>2007<\/b>, <i>48<\/i>, 2139-2141.<\/li>\n<li>Chen, P. Y.; Chen, H. M.; Chen, L. Y.; Tzeng, J. Y.;\u00a0 Tsai, J. C.; Chi, P. C.; Li, S. R.;\u00a0 <b>Wang, E. C. *<\/b> \u201cClaisen rearrangement\/Baylis-Hillman reaction\/ring-closing metathesis as bases for the construction of substituted cyanonaphthalenes.\u201d <i>Tetrahedron <\/i><b>2007<\/b>, <i>63<\/i>, 2824-2828.<\/li>\n<li><b>Wang, E. C.; <\/b>Wein, Y. S.; Kuo, Y. H.*, \u201cA concise and efficient Synthesis of Salvinal from Isoeugenal via a Phenoxenium ion Intermediate\u201d<i>Tetrahedron<\/i><i> Lett. <\/i><b>2006<\/b>, <i>47<\/i>, 9195-9197.<\/li>\n<li>Hou, D. R.*; Cheng, H. Y.; <b>Wang, E. C.<\/b> \u201cEfficient Synthesis of Oncinotine and Neooncinotine\u201d <i>J. Org. Chem<\/i>. <b>2004<\/b>, <i>69<\/i>, 6094-6099.<\/li>\n<li>Tsai, T. W. ; <b>Wang, E. C.*; <\/b>Li, S. R.;\u00a0 Chen, H. M.; Lin, Y. L.;\u00a0 Wang, Y. F.; Huang, K.S. \u201cA New Synthesis of Benzofurans from Phenols <i>via <\/i>Claisen Rearrangement and Ring-Closing Metathesis \u201d<i>J. Chin. Chem.<\/i> <i>Soc. <\/i><b>2004<\/b>, <i>51(6)<\/i>, 1307-1318.<\/li>\n<li>Tsai, T. W.; <b>Wang, E. C.*<\/b> \u201cA new synthesis of angelicin from 7-hydroxycoumarin via <i>C<\/i>-propenation-<i>O<\/i>-vinylation and ring-closing metathesis\u201d <i>J. Chin. Chem. Soc. <\/i><b>2004<\/b>, <i>51(5)<\/i>, 1019-1024.<\/li>\n<li><b>Wang, E. C.*;<\/b> Huang, K. S.; Chen, H. M.; Wu, C. C.;\u00a0 Lin, G. J.\u00a0 \u201cAn efficient method for the preparation of nitriles via the dehydration of aldoximes with phthalic anhydride\u201d<i>J<\/i><i>. Chin. Chem. Soc.<\/i> <b>2004<\/b>, <i>51 <\/i>(3), 619-627.<\/li>\n<li>Hou, D. R.*; Cheng, H. Y.; <b>Wang, E. C.<\/b> \u201cEfficient Synthesis of Oncinotine and Neooncinotine\u201d <i>J. Org. Chem<\/i>. <b>2004<\/b>, <i>69<\/i>, 6094-6099.<\/li>\n<li>Huang, K. S.; <b>Wang, E. C.*<\/b> \u201cSynthesis of Substituted Indenes from Isovanillin via Claisen Rearrangement and RCM\u201d <i>J. Chin. Chem. Soc<\/i>. <b>2004<\/b>, <i>51<\/i>, 383-391.<\/li>\n<li>Huang, K. S.; <b>Wang, E. C.*<\/b>; Chen, H. M.\u00a0 \u201cSynthesis of 4-Alkoxy-3-methoxy &#8211; 5H- benzocycloheptenes and 2-Alkoxy-3-methoxy-5H-benzocycloheptenes\u201d<i>J. Chin, Chem. Soc<\/i>. <b>2004<\/b>, <i>51<\/i>, 807-816.<\/li>\n<li>Tsai, T. W.; <b>Wang, E. C.*<\/b>; Huang, K. S.; Li, S. R. ; Wang , Y. F. ; Lin, Y. L. ; Chen, Y. H. \u201cSynthesis of Benzofurans from Isovanillin via C-propenylation-O-vinylation and Ring-closing metathesis\u201d <i>Heterocycles<\/i><\/li>\n<li>Huang, K. S.; <b>Wang, E. C.*<\/b>; Chen, H. M.\u00a0 \u201cSynthesis of Naphthalenes and\u00a0\u00a0 Naphthols\u201d <i>J. Chin. Chem. Soc<\/i>. <b>2004<\/b>, <i>51<\/i>, 585-605.<\/li>\n<li><b>Wang, E. C.<\/b>*; Chen, H. F. ; Feng, P. K. ; Lin, Y. L.; Hsu, M. K. \u201cA New Synthesis of 3-Alkyl-1-Isoindolinones\u201d<i> Tetrahedron Lett<\/i>.<b> 2002<\/b>, <i>43(50)<\/i>, 9163-9165.<\/li>\n<li>Huang, K. S.; <b>Wang, E. C.<\/b>* \u201cA Novel Synthesis of Substituted Naphthalenes <i>via<\/i> Claisen Rearrangement and RCM Reaction\u201d<i> Tetrahedron Lett<\/i>.<b> 2001<\/b>, 42, 6155-6157.<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>Paper published (2012-2009) Chen, Po-Yua &hellip; <a href=\"https:\/\/wp.kmu.edu.tw\/enchwa\/%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":30,"featured_media":0,"parent":0,"menu_order":0,"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-8","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/wp.kmu.edu.tw\/enchwa\/wp-json\/wp\/v2\/pages\/8","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/wp.kmu.edu.tw\/enchwa\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/wp.kmu.edu.tw\/enchwa\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/wp.kmu.edu.tw\/enchwa\/wp-json\/wp\/v2\/users\/30"}],"replies":[{"embeddable":true,"href":"https:\/\/wp.kmu.edu.tw\/enchwa\/wp-json\/wp\/v2\/comments?post=8"}],"version-history":[{"count":2,"href":"https:\/\/wp.kmu.edu.tw\/enchwa\/wp-json\/wp\/v2\/pages\/8\/revisions"}],"predecessor-version":[{"id":10,"href":"https:\/\/wp.kmu.edu.tw\/enchwa\/wp-json\/wp\/v2\/pages\/8\/revisions\/10"}],"wp:attachment":[{"href":"https:\/\/wp.kmu.edu.tw\/enchwa\/wp-json\/wp\/v2\/media?parent=8"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}