Education
School ¡X Major ¡X Degree | Duration |
---|---|
°ª¶¯Âå¾Ç°| ¡X ÃľǬã¨s©Ò(²¦) ¡X ³Õ¤h Doctorate, , |
¡X 1992/06 |
°ª¶¯Âå¾Ç°| ¡X ÃľǬã¨s©Ò(²¦) ¡X ºÓ¤h Master, , |
¡X 1988/06 |
°ª¶¯Âå¾Ç°| ¡X ÃľǨt(²¦) ¡X ¾Ç¤h Bachelor, , |
¡X 1983/06 |
Intramural Experience
Office/Department/Institute | Position | Duration |
---|---|---|
Ãľǰ| College of Pharmacy | Dean | 2024/02/01 ¡X 2027/01/31 |
ÃľǨt School of Pharmacy | Professor | 2016/02/01 ¡X |
»ùÛ«~¾Ç¨t Department of Fragrance and Cosmetic Science | Professor | 2013/08/01 ¡X 2016/01/31 |
ÃľǨt School of Pharmacy | Professor | 2001/08/01 ¡X 2013/07/31 |
ÃľǨt School of Pharmacy | Associate Professor | 1992/08/01 ¡X 2001/07/31 |
ÃľǨt School of Pharmacy | Lecturer | 1988/08/01 ¡X 1992/07/31 |
ÃľǨt School of Pharmacy | Teaching Assistant | 1987/08/01 ¡X 1988/07/31 |
Extramural Experience
Discipline
NO | Discipline | Expertise |
---|---|---|
1 | ¥Íª«Âå¹AÃþ Biology, Medicine and Agriculture | ÃľǤΤ¤ÂåÃÄ Pharmacy and Chinese Medicine and Pharmacy |
2 | ¦ÛµM¬ì¾ÇÃþ Natural Sciences | ¤Æ¾Ç Chemistry |
Research & Technology Platform Open to the Outside
Interested Area(s)for Interdisciplinary Research
Organic Synthesis, Organometallics, Medicinal Chemistry, Green Chemistry
Area(s) of Expertise & Research
¦³¾÷¦X¦¨¡F¦³¾÷ª÷ÄݤƾǡFÃĪ«¤Æ¾Ç¡Fºñ¦â¤Æ¾Ç
Organic Synthesis, Organometallics, Medicinal Chemistry, Green Chemistry
Publication
NO | Publication |
---|---|
1 | Family Malvaceae: a potential source of secondary metabolites with chemopreventive and anticancer activities supported with pharmacokinetic and pharmacodynamic profiles. Family Malvaceae: a potential source of secondary metabolites with chemopreventive and anticancer activities supported with pharmacokinetic and pharmacodynamic profiles. |
2 | Xestoquinone¬O¤@ºØ¦³®Äªº©Ý¼³²§ºc酶 II ©M HSP90 Âù«§í»s¾¯¡A¨ä³q¹L ROS »¤¾É¨Ó§í¨îHSP-90¥HªvÀø¥Õ¦å¯f The Antileukemic Effect of Xestoquinone, A Marine-Derived Polycyclic Quinone-Type Metabolite, Is Mediated through ROS-Induced Inhibition of HSP-90 |
3 | ¦b¤ô¤¤§Q¥Î¹`¶Ê¤Æ2,3-¤G¸m´«吲哚Ãþ»P²m¤þàÃþ¶i¦æ¿ï¾Ü©Êªº´á-²m¤þ°ò¤Æ¤ÏÀ³ Platinum-catalyzed selective N-allylation of 2,3-disubstituted indoles with allylic acetates in water |
4 | ÂǥѻE¤A¤G¾J-¤ô¨t²Î§Q¥ÎÜj¶Ê¤Æ¨Ï吲哚Ãþ¶i¦æ¿ï¾Ü©Êªº´á-²m¤þ°ò¤Æ¤ÏÀ³ Palladium-catalyzed selective N-allylation of indoles assisted by PEG¡Vwater system |
5 | ¤pªGÁ¥Á¨¤A¾JµÑ¨úª«ÂÇ¥ÑIn Vitro©MIn Vivo¸ÕÅç¡A±´°Q¬¡¤ÆPhosphatase©MTensin Homolog¹F¨ì§Ü¦åÀù ¡G§Ü¥Õ¦å¯f¬ã¨s·sª¾ The Antioxidant from Ethanolic Extract of Rosa cymosa Fruits Activates Phosphatase and Tensin Homolog In Vitro and In Vivo: A New Insight on Its Antileukemic Effect |
6 | ´¸Ãþªº³sÄò¬y²B¤Æ©MÁÙ쫲B¤ÏÀ³¡G¤@ºØ²³æ±o¨ì£\,£\-Dideutero Aminesªº¤èªk Continuous-Flow Hydrogenation and Reductive Deuteration of Nitriles: a Simple Access to £\,£\-Dideutero Amines |
7 | §Q¥Î¹`¶Ê¤Æ¨Ï2,3-¤G¸m´«吲哚Ãþ»P²m¤þàÃþ¶i¦æ²m¤þ°ò¤Æ¤ÏÀ³ Platinum-Catalyzed Allylation of 2,3-Disubstituted Indoles with Allylic Acetates |
8 | §Q¥Î½Þ¼Ò«¬Æ[¹î¨Ï¥Î¸¡¥D°Ê¯ß¤º¨T²y³y¦¨¦AÄéª`¶Ë®`ªº¯f¥Í²zÅÜ¤Æ Porcine model for observing changes due to ischemia/reperfusion injury secondary to intra-abdominal endovascular balloon occlusion |
9 | ª÷µ·®çÂǥѧí¨îNFkB¤Î¬¡¤ÆNrf2³~®|´î½w¹«¼Ò«¬¤§cisplatinµÇ¬r©Ê Hyperin inhibits nuclear factor kappa B and activates nuclear factor E2-related factor-2 signaling pathways in cisplatin-induced acute kidney injury in mice |
10 | ±´¯Á·s«¬N-alkyl 4-anilinofuro[2,3-b]quinoline (CIL-102)l¥Íª«¹ï«e¦C¸¢Àù²ÓM¤§§@¥Î Discovery of Novel N-alkyl 4-anilinofuro[2,3-b]quinoline Derivatives (CIL-102 Derivatives) Against Castration-Resistant Human Prostate Cancers |
11 | ±´¯Á§t§c°ò萘l¥Íª«§@¬°Nrf2¿E¬¡¾¯ªº·s«¬µ²ºc Discovery of oxime-bearing naphthalene derivatives as a novel structural type of Nrf2 activators |
12 | ·s«¬§t§c»¨§¯Àl¥Íª«©óÅé¥~©M¤p¹«¼Ò¦¡¹êÅç§@¬°¦³®ÄªºNrf2/ARE¿E¬¡¾¯ Novel oxime-bearing coumarin derivatives act as potent Nrf2/ARE activators in vitro and in mouse model |
13 | Lantabetulic»Äl¥Íª«»¤¾É¤HÃþ«e¦C¸¢Àù²ÓMG1´Áªýº¢©Mä¤` Lantabetulic Acid Derivatives Induce G1 Arrest and Apoptosis in Human Prostate Cancer Cells |
14 | ¦X¦¨fÓi喹ªLl¥Íª«¨ÃÂǥѦbpolo-like kinaseªí²{ªº®ÄÀ³¨Óµû¦ô¨ä§Ü¸~½F¬¡©Ê Synthesis and antitumor activity evaluation of anilinoquinoline derivatives by the effect on the expression of polo-like kinase |
15 | ¦b¥xÆWMethyltetrahydrofolate Reductase (MTHFR) Polymorphisms»P¤ÀÂ÷ªº¶}©ñ©Ê°Ê¯ß¾ÉºÞ¤§¶¡ªºÃö³s¬ã¨s Correlation Between Methyltetrahydrofolate Reductase (MTHFR) Polymorphisms and Isolated Patent Ductus Arteriosus in Taiwan |
16 | Âǥѻ¤¾É¤zÂZ¯À§Ü¯f¬r¤ÏÀ³ªº·s«¬§ÜC«¬¨xª¢¯f¬r»s¾¯-fÓi»¨§¯ÀÃþl¥Íª« Novel anilinocoumarin derivatives as agents against hepatitis C virus by the induction of IFN-mediated antiviral responses |
17 | Anti-hepatitis C virus RdRp activity and replication of novel anilinobenzothiazole derivatives Anti-hepatitis C virus RdRp activity and replication of novel anilinobenzothiazole derivatives |
18 | ±qGanoderma tsugae¤ÀÂ÷ªº lanostanoids ¹ï¶ÀáIËï®ñ¤Æ酶ªº§í¨î Xanthine oxidase inhibitory lanostanoids from Ganoderma tsugae |
19 | ¦b¤ô¤¤§Q¥Î²³æªºÜj¶Ê¤Æ¾¯¶i¦æµL¬¡¤Æ¾¯¤@³ýªººÒ-²m¤þ°ò¤Æ¤ÏÀ³ Activator-free and one-pot C-allylation by simple palladium catalyst in water |
20 | Anilinoquinolinel¥Íª«ªº¦X¦¨¤Î§ÜC¨x¬¡©Êµû¦ô Synthesis and anti-HCV activity evaluation of anilinoquinoline derivatives |
21 | Secondary metabolites from the stems of Engelhardia roxburghiana and their antitubercular activities Secondary metabolites from the stems of Engelhardia roxburghiana and their antitubercular activities |
22 | ºÖ¤ì¦¨¤Àªº²ÓM¬r©Ê©M§Ü®ñ¤Æ Cytotoxic and antioxidant constituents from Garcinia subelliptica |
23 | ¦b¤ô¤¤§Q¥ÎPEG-4000«P¶iÜj¶Ê¤Æ´á¡X²m¤þ°ò¤Æ¤ÏÀ³¡G¥H©`ÓiÃþ¬°¨Ò PEG-4000 promoted palladium-catalyzed N-allylation in water: Aminonaphthalene as an example |
24 | Guttiferaceous´Óª«¤¤ªºXanthine oxidase§í¨î¦¨¤Àtriterpenoid and phloroglucinol³z¹LROS¾÷¨î»¤¾ÉNTUB1²ÓMªºä¤` Xanthine oxidase inhibitory triterpenoid and phloroglucinol from guttiferaceous plants inhibit growth and induced apoptosis in human NTUB1 cells through a ROS-dependent mechanism. |
25 | Antioxidant xanthonel¥Íª«³z¹LROS¥[±jcisplatin¹ïNTUB1²ÓMªº¬r±þ§@¥Î Antioxidant xanthone derivatives induce cell cycle arrest and apoptosis and enhance cell death induced by cisplatin in NTUB1 cells associated with ROS. |
26 | 18£]-Glycyrrhetinic acid derivatives induced mitochondrial-mediated apoptosis through reactive oxygen species-mediated p53 activation in NTUB1 cells 18£]-Glycyrrhetinic acid derivatives induced mitochondrial-mediated apoptosis through reactive oxygen species-mediated p53 activation in NTUB1 cells |
27 | ±qNelumbo nucifera Gaertn. cv. Rosa-plenaªº¸¤l¤ÀÂ÷¥Xªº¤Æ¾Ç¦¨¤À Chemical constituents from the leaves of Nelumbo nucifera Gaertn. cv. Rosa-plena |
28 | ±qMomordica charantiaªº²ô»PªG¹ê¤ÀÂ÷±o¨ìªº§Ü®ñ¤Æ¦¨¤À Antioxidant constituents from the stems and fruits of Momordica charantia |
29 | §Q¥Î²³æªºÜj¶Ê¤Æ¨Ï®z¿Ë®Ö©Êªº©`ÓiÃþ¶i¦æºÒ-´áÁ䪺§Î¦¨ Simple palladium-catalyzed C-N bond formation for poor nucleophilicity of aminonaphthalenes |
30 | Anthraquinone derivatives¦b»H¯ÖÀù²ÓM»¤µoG2/M arrest ©Mapoptosis Anthraquinone derivatives induce G2/M cell cycle arrest and apoptosis in NTUB1 cells |
31 | §Q¥Î¸K½Õ¸Ñ²mÂùÍPÃþ¶i¦æ¤À¬qÀô¤Æ¤ÏÀ³±o¨ì¸K¤ÆªºBenzo[a]carbazoles Iodine-Mediated Cascade Cyclization of Enediynes to Iodinated Benzo[a]carbazoles |
32 | 2',5'-dimethoxychalcone l¥Íª«¤§¦X¦¨»P§@¥Î©ó·LºÞ¤§¬¡©Êµû¦ô Synthesis and biological evaluation of 2',5'-dimethoxychalcone derivatives as microtubule-targeted anticancer agents |
33 | ±qCinnamomum subavenium®Ú³¡ªº¤Æ¾Ç¦¨¤À Chemical constituents from the roots of Cinnamomum subavenium |
34 | ±qMichelia compresa var. lanyuensis²ô³¡ªº¤Æ¾Ç¦¨¤À Chemical Constituents from the Stems of Michelia compressa VAR. lanyuensis |
35 | ´ÄÃq¥Í¨|¤T²m¾JªºÅ@¨x¥\®Äµû¦ô Hepatoprotection by palm tocotrienol-rich fraction |
36 | ±q¥xÆWÁJªá§ü¤ÀÂ÷±o¨ì¨ã¦³§í¨î¶ÀáIËï®ñ¤Æ酶ªº¤T©«;Ãþ¡A¦b¥¿±`¤HÃþ§¿¹D¤W¥Ö²ÓM»P »H¯ÖÀù²ÓM¤¤¯àÂǥѴî¤Ö¬¡©Ê®ñ¨Ó«OÅ@cispplatin»¤µo¤§²ÓM¦º¤` Xanthine oxidase inhibitory terpenoids of Amentotaxus formosana protect cisplatin-induced cell death by reducing reactive oxygen species (ROS) in normal human urothelial and bladder cancer cells |
37 | §Q¥ÎÜj¡]II¡^¶Ê¤Æ²mÂù¯ÊÃþ¶i¦æÀô¤Æ¤ÏÀ³§Î¦¨benzo[a]carbazolesªº¦X¦¨§Y¤©¤ÏÀ³¾÷¨î±´°Q Synthetic development and mechanistic study on Pd(II)-catalyzed cyclization of enediynes to benzo[a]carbazoles |
38 | ¶Àà¬Ãþl¥Íª«ªº¦X¦¨¡B§Ü¦å¤pªO»P¦åºÞÂX±i¬¡©Ê Synthesis, antiplatelet and vasorelaxing activities of xanthone derivatives |
39 | 1-(2-((Z)-6-(2-(Trifluoromethyl)phenyl)hexa-3-en-1,5-diynyl)-piperidin-2-one ¥i¯à¦¨¬°¨ã¦³¼ç¤Oªº²ÓMä¤`Ãľ¯ 1-(2-((Z)-6-(2-(Trifluoromethyl)phenyl)hexa-3-en-1,5-diynyl)-piperidin-2-one as a new potent apoptosis agent |
40 | Ursolic acidl¥Íª«¦bNTUB1²ÓM¤¤³z¹L²£¥Í¦Û¥Ñ°ò¤Þµo²ÓM¶g´Á°±º¢¤Îä¤` Ursolic acid derivatives induce cell cycle arrest and apoptosis in NTUB1 cells associated with reactive oxygen species |
41 | Phloroglucinols§í¨îchemical mediators and xanthine oxidase¨Ã¦b»H¯Ö¤W¥Ö²ÓM¤¤³z¹L´î¤Ö¦Û¥Ñ°ò©è§Ücisplatin»¤µoªº²ÓMä¤` Phloroglucinols inhibit chemical mediators and xanthine oxidase, and protect cisplatin-induced cell death by reducing reactive oxygen species in normal human urothelial and bladder cancer cells. |
42 | §Q¥Î·Lªi¨Ï 2-alkynylbenzonitriles»PÅ|´á¤Æ¶u¶i¦æÀô¥[¦¨¤ÏÀ³¡G¿ï¾Ü©Ê¦a¦X¦¨tetrazolo[5,1-a]pyridines and 4,5-disubstituted-2H-1,2,3- triazoles Microwave-assisted cycloadditions of 2-alkynylbenzonitriles with sodium azide: selective synthesis of tetrazolo[5,1-a]pyridines and 4,5-disubstituted-2H-1,2,3- triazoles |
43 | 18b-glycyrrhetinic acidl¥Íª«ªº¦X¦¨¡B§Üµoª¢¡B§Ü®ñ¤Æ¬¡©Ê Synthesis, anti-inflammatory, and antioxidant activities of 18b-glycyrrhetinic acid derivatives as chemical mediators and xanthine oxidase inhibitors |
44 | ¦b¤ô¤¤ª½±µ§Q¥ÎÜj/ßn»Ä¶Ê¤ÆÀô1,3-¤Gà¬Ãþ»P²m¤þ¾JÃþ¶i¦æºÒ-²m¤þ°ò¤Æ¤ÏÀ³ Direct palladium/carboxylic acid-catalyzed C-allylation of cyclic 1,3-diones with allylic alcohols in water |
45 | Cell death induced by flavonoid glycosides with and without copper Cell death induced by flavonoid glycosides with and without copper |
46 | Phloroglucinols with prooxidant activity from Garcinia subelliptica Phloroglucinols with prooxidant activity from Garcinia subelliptica |
47 | Synthesis and cytotoxic, anti-inflammatory, and anti-oxidant activities of 2',5'-dialkoxylchalcones as cancer chemopreventive agents Synthesis and cytotoxic, anti-inflammatory, and anti-oxidant activities of 2',5'-dialkoxylchalcones as cancer chemopreventive agents |
48 | Phloroglucinols with antioxidant activity and xanthonolignoids from the heartwood of Hypericum geminiflorum Phloroglucinols with antioxidant activity and xanthonolignoids from the heartwood of Hypericum geminiflorum |
49 | ¦b¤ô¤¤§Q¥Î¹`¶Ê¤Æ©`ÓiÃþ»P²m¤þàÃþ¶i¦æ²m¤þ°ò¤Æ¤ÏÀ³ Platinum-catalyzed allylation of aminonaphthalenes with allylic acetates in water |
50 | 2-(6-aryl-3(Z)-hexen-1,5-diynyl)anilines ¬O¤@Ó·s«¬ªºantitubulin¸Õ¾¯ 2-(6-aryl-3(Z)-hexen-1,5-diynyl)anilines as a new class of potent antitubulin agents |
51 | 2-(6-aryl-3(Z)-hexen-1,5-diynyl) fÓiÃþ§@¬°¤@Ãþ·sªº±j¦³¤O§Ü·LºÞ³J¥Õ¾¯¡C 2-(6-aryl-3(Z)-hexen-1,5-diynyl)anilines as a new class of potent antitubulin agents. |
52 | §Q¥Î¹`¶Ê¤Æ©`ÓiÃþ»P¤A»Ä²m¤þàÃþ¶i¦æ²m¤þ°ò¤Æ¤ÏÀ³ Platinum-catalyzed allylation of aminonaphthalenes with allylic acetates |
53 | ¦b¤ô¤¤ª½±µ§Q¥Î²m¤þ¾JÃþ¶i¦æÜj/ßn»Ä¶Ê¤ÆfÓiÃþ²m¤þ°ò¤Æ¤ÏÀ³ Direct palladium/carboxylic acid-catalyzed allylation of anilines with allylic alcohols in water |
54 | ª½±µ§Q¥Î²m¤þ¾JÃþ¶i¦æÜj¶Ê¤Æ»Ä©Ê¤Î¤Ö¿Ë®Ö©ÊfÓiÃþ¶i¦æ²m¤þ°ò¤Æ¤ÏÀ³ Palladium-catalyzed allylation of acidic and less nucleophilic anilines using allylic alcohols directly |
55 | §Q¥Î2-¤B²m-1,4-¤G¾J¨Ï2-Ói×ôÃþ¶i¦æÜj¶Ê¤Æ¦ì¦V¯S²§©Ê«e«á¨â¦¸²m¤þ°ò¤Æ¤ÏÀ³ Palladium-catalyzed regiospecific tandem allylation of 2-aminophenols using 2-butene-1,4-diol |
56 | §Q¥ÎÜj¶Ê¤Æ¨Ï1,2-f¤GÓi»P¶¶-1,4-¤G¤AñQ®ñ°ò-2-¤B²m¶i¦æ«e«á¨â¦¸²m¤þ°ò¤Æ¤ÏÀ³ Palladium-catalyzed tandem allylation of 1,2-phenylenediamines with cis-1,4-diacetoxy-2-butene |
57 | ª½±µ§Q¥Î©`ÓiÃþ¤Æ¦Xª«¨Ï²m¤þ¾JÃþ¤Æ¦Xª«¶i¦æÜj¶Ê¤ÆÓi¤Æ¤ÏÀ³ Direct palladium(0)-catalyzed amination of allylic alcohols with aminonaphthalenes |
58 | ª½±µ§Q¥Î2-¤B²m-1,4-¤G¾J¨Ï¾F-f¤GÓiÃþ¤Æ¦Xª«¶i¦æÜj¶Ê¤Æ«e«á¨â¦¸²m¤þ°ò¤Æ¤ÏÀ³ Palladium-catalyzed tandem allylation of o-phenylenediamines using 2-butene-1,4-diol directly |
59 | ª½±µ§Q¥Î²m¤þ¾JÃþ¤Æ¦Xª«¨ÏfÓiÃþ¤Æ¦Xª«¶i¦æ¹`¶Ê¤Æ²m¤þ°ò¤Æ¤ÏÀ³ Direct platinum-catalyzed allylation of anilines using allylic alcohols |
60 | ª½±µ§Q¥Î²m¤þ¾JÃþ¤Æ¦Xª«¨ÏfÓiÃþ¤Æ¦Xª«¶i¦æÜj¶Ê¤Æ²m¤þ°ò¤Æ¤ÏÀ³ªº¦ì¦V©M¥ßÅé¿ï¾Ü©Ê Regio- and stereoselectivity in palladium(0)-catalyzed allylation of anilines using allylic alcohols directly |
61 | §Q¥ÎÜj¶Ê¤Æ´á¡X¡]2¡XÀô¤v²m¡^·Í¤Æ¤AñQÓiÃþl¥Íª«ªºÀô¤Æ¤ÏÀ³¦X¦¨¤f¤ñ¤f¦UÔrÃþl¥Íª« The synthesis of pyrrolidine derivatives by the palladium-catalyzed cyclization of N-(2-cyclohexenyl)bromoacetamide derivatives |
62 | §Q¥ÎfÓiÃþ¤Æ¦Xª«¶i¦æÜj¶Ê¤Æ²m¤þ¾JÃþ¤Æ¦Xª«ªºÓi¤Æ¤ÏÀ³ Palladium-catalyzed amination of allylic alcohols using anilines |
63 | ¦b¥|²§¤þ®ñ°òÜgªº¦s¦b¤U¡Aª½±µ§Q¥Î²m¤þ¾JÃþ¤Æ¦Xª«¶i¦æÜj¶Ê¤ÆfÓiÃþ¤Æ¦Xª«ªº´á¡X²m¤þ°ò¤Æ¤ÏÀ³ Palladium-catalyzed N-allylation of anilines by direct use of allyl alcohols in the presence of titanium(IV) isopropoxide |
64 | Üj¶Ê¤Æ¦X¦¨5¡X©M5,7¡X¸m´«¤f¤Þ¤f¦·Ãþl¥Íª« Palladium-catalyzed synthesis of 5- and 5,7-substituted indole derivatives |
65 | ª½±µ§Q¥Î²m¤þ¾JÃþ¤Æ¦Xª«¶i¦æ¤@ºØ¦³®ÄªºÜj¶Ê¤Æ¸ô®|§Î¦¨´á¡X²m¤þ°òÓiÃþ¤Æ¦Xª« An efficient, palladium-catalyzed route to N-allylanilines by direct use of allyl alcohols |
Project
NO |
YEAR ¡X Source ¡X No ¡X Type
Project Name
|
Duration |
---|---|---|
1 |
105 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X MOST105-2113-M-037-017 ¡X 1 Ó¤H«¬
¦bºñ¦â¤Æ¾Ç¤W§Q¥ÎÔB¶Ê¤Æ²m¤þ°òÖJ¤Æ¤ÏÀ³( )
|
2016/08/01 ~ 2018/07/31 |
2 |
104 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X MOST104-2113-M-037-002 ¡X 1 Ó¤H«¬
¦bºñ¦â¤Æ¾Ç¤W§Q¥Î©`¦Ìª÷ÄݶʤƧt´á¤Æ¦Xª«¶i¦æ²m¤þ°ò¤Æ¤ÏÀ³ªº¬ã¨s( )
|
2015/08/01 ~ 2016/07/31 |
3 |
103 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC101-2113-M-037-008-MY3 ¡X 1 Ó¤H«¬
¦bºñ¦â¤Æ¾Ç¤W§Q¥Îª÷Äݶʤƿï¾Ü©Ê¦a§Î¦¨ºÒ-ºÒ¡BºÒ-´á¤ÎºÒ-®ñÁ䪺¬ã¨s(3/3)( )
|
2014/08/01 ~ 2015/07/31 |
4 |
102 ¡X H ½ÃºÖ³¡ ¡X 102TFDA-MD-038 ¡X
¤ÆùÛ«~Á{§É¸ÕÅ礤¤ß³W¹ºº[¦w¥þºÞ²z¬ã¨s( )
|
2013/09/06 ~ 2013/12/31 |
5 |
102 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC101-2113-M-037-008-MY3 ¡X 1 Ó¤H«¬
¦bºñ¦â¤Æ¾Ç¤W§Q¥Îª÷Äݶʤƿï¾Ü©Ê¦a§Î¦¨ºÒ-ºÒ¡BºÒ-´á¤ÎºÒ-®ñÁ䪺¬ã¨s(2/3)( )
|
2013/08/01 ~ 2015/07/31 |
6 |
101 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC101-2113-M-037-008-MY3 ¡X 1 Ó¤H«¬
¦bºñ¦â¤Æ¾Ç¤W§Q¥Îª÷Äݶʤƿï¾Ü©Ê¦a§Î¦¨ºÒ-ºÒ¡BºÒ-´á¤ÎºÒ-®ñÁ䪺¬ã¨s(1/3)( )
|
2012/08/01 ~ 2015/07/31 |
7 |
100 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC98-2119-M-037-001-MY3 ¡X 1 Ó¤H«¬
¦bºñ¦â¤Æ¾Ç¤W§Q¥Îª÷Äݶʤƶi¦æ²m¤þ°ò¤Æ¤ÎªÚ»¤Æ¤ÏÀ³ªº¬ã¨s(3/3)( )
|
2011/08/01 ~ 2012/07/31 |
8 |
099 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC98-2119-M-037-001-MY3 ¡X 1 Ó¤H«¬
¦bºñ¦â¤Æ¾Ç¤W§Q¥Îª÷Äݶʤƶi¦æ²m¤þ°ò¤Æ¤ÎªÚ»¤Æ¤ÏÀ³ªº¬ã¨s(2/3)( )
|
2010/08/01 ~ 2012/07/31 |
9 |
098 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC98-2119-M-037-001-MY3 ¡X 1 Ó¤H«¬
¦bºñ¦â¤Æ¾Ç¤W§Q¥Îª÷Äݶʤƶi¦æ²m¤þ°ò¤Æ¤ÎªÚ»¤Æ¤ÏÀ³ªº¬ã¨s(1/3)( )
|
2009/08/01 ~ 2012/07/31 |
10 |
098 ¡X Z ¤j±M¾Ç¥Í¬ã¨spµe¤Î³Õ¤h«á ¡X NSC99-2815-C-037-025-M ¡X 8 ¤j±M¾Ç¥Í¬ã¨spµe
99¦~«×¤j±M¾Ç¥Í°Ñ»P±MÃD¬ã¨spµe-¤ý¸Ö²[( )
|
2010/07/01 ~ 2011/02/28 |
11 |
097 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC95-2113-M-037-011-MY3 ¡X 1 Ó¤H«¬
¦bÀô«O¤Æ¾Ç¤W§Q¥ÎÜj¤Î¹`¶Ê¤Æ²m¤þ°ò¤Æ¤ÎªÚ»¤Æ¤ÏÀ³(3/3)( )
|
2008/08/01 ~ 2009/07/31 |
12 |
097 ¡X Z ¤j±M¾Ç¥Í¬ã¨spµe¤Î³Õ¤h«á ¡X 98-2815-C-037-025-B ¡X 8 ¤j±M¾Ç¥Í¬ã¨spµe
98¦~«×¤j±M¾Ç¥Í°Ñ»P±MÃD¬ã¨spµe--³¯¦ö¦p( )
|
2009/07/01 ~ 2010/02/28 |
13 |
096 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC95-2113-M-037-011-MY3 ¡X 1 Ó¤H«¬
¦bÀô«O¤Æ¾Ç¤W§Q¥ÎÜj¤Î¹`¶Ê¤Æ²m¤þ°ò¤Æ¤ÎªÚ»¤Æ¤ÏÀ³(2/3)( )
|
2007/08/01 ~ 2009/07/31 |
14 |
096 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC96-2745-M-037-003-URD ¡X 2 ¾ã¦X«¬
¥Íª«¬¡©Ê¤À¤l¿z¿ï¤¤¤ß-(¤lpµe¤T):ÐüÃþ¥Íª«ÆPl¥Íª«ªº»s³Æ¤Î§ÜÀùµû¦ô(3/3)( )
|
2007/08/01 ~ 2008/07/31 |
15 |
095 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC95-2113-M-037-011-MY3 ¡X 1 Ó¤H«¬
¦bÀô«O¤Æ¾Ç¤W§Q¥ÎÜj¤Î¹`¶Ê¤Æ²m¤þ°ò¤Æ¤ÎªÚ»¤Æ¤ÏÀ³(1/3)( )
|
2006/08/01 ~ 2009/07/31 |
16 |
095 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC95-2745-M-037-001-URD ¡X 2 ¾ã¦X«¬
¥Íª«¬¡©Ê¤À¤l¿z¿ï¤¤¤ß-(¤lpµe¤T):ÐüÃþ¥Íª«ÆPl¥Íª«ªº»s³Æ¤Î§ÜÀùµû¦ô(2/3)( )
|
2006/08/01 ~ 2007/07/31 |
17 |
094 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC94-2113-M-037-005- ¡X 1 Ó¤H«¬
§Q¥Îª÷Äݶʤƶi¦æ²m¤þ°ò¤Æ©MÓi¤Æ¤ÏÀ³ªº¬ã¨s( )
|
2005/08/01 ~ 2006/07/31 |
18 |
094 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC94-2745-M-037-003-URD ¡X 2 ¾ã¦X«¬
¥Íª«¬¡©Ê¤À¤l¿z¿ï¤¤¤ß-(¤lpµe¤T):ÐüÃþ¥Íª«ÆPl¥Íª«ªº»s³Æ¤Î§ÜÀùµû¦ô(1/3)( )
|
2005/08/01 ~ 2006/07/31 |
19 |
094 ¡X Z ¤j±M¾Ç¥Í¬ã¨spµe¤Î³Õ¤h«á ¡X NSC95-2815-C-037-003-M ¡X 8 ¤j±M¾Ç¥Í¬ã¨spµe
¤j±M´»´Ápµe--¤ýÄR¶®( )
|
2006/07/01 ~ 2007/02/28 |
20 |
093 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC93-2113-M-037-008- ¡X 1 Ó¤H«¬
¦b¤ô¤¤ª½±µ§Q¥Î²m¤þ¾JÃþ¶i¦æÜj©M¹`¶Ê¤Æ´á¡X©MºÒ¡X²m¤þ°ò¤Æ¤ÏÀ³ªº¬ã¨s( )
|
2004/08/01 ~ 2005/07/31 |
21 |
093 ¡X Z ¤j±M¾Ç¥Í¬ã¨spµe¤Î³Õ¤h«á ¡X NSC94-2815-C-037-002-M ¡X 8 ¤j±M¾Ç¥Í¬ã¨spµe
( )
|
2005/07/01 ~ 2006/02/28 |
22 |
092 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC92-2113-M-037-025- ¡X 1 Ó¤H«¬
ª½±µ§Q¥Î²m¤þ¾JÃþ¤Æ¦Xª«¶i¦æÜj©M¹`¶Ê¤Æ²m¤þ°ò¸m´«¤ÏÀ³ªº¬ã¨s(3/3)( )
|
2003/08/01 ~ 2004/07/31 |
23 |
091 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC91-2113-M-037-005 ¡X 1 Ó¤H«¬
ª½±µ§Q¥Î²m¤þ¾JÃþ¤Æ¦Xª«¶i¦æÜj©M¹`¶Ê¤Æ²m¤þ°ò¸m´«¤ÏÀ³ªº¬ã¨s(2/3)( )
|
2002/08/01 ~ 2006/07/31 |
24 |
090 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC90-2113-M-037-017 ¡X 1 Ó¤H«¬
ª½±µ§Q¥Î²m¤þ¾JÃþ¤Æ¦Xª«¶i¦æÜj©M¹`¶Ê¤Æ²m¤þ°ò¸m´«¤ÏÀ³ªº¬ã¨s(1/3)(Palladium- and Platinum-Catalyzed Allylic Substitution Using Allylic Alcohols Directly)
|
2001/08/01 ~ 2002/07/31 |
25 |
089 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC 89-2113-M-037-027- ¡X 1 Ó¤H«¬
ª½±µ§Q¥Î²m¤þ¾JÃþ¤Æ¦Xª«¶i¦æÜj¶Ê¤Æ²m¤þ°òÓi¤Æ¤ÏÀ³ªº¥ßÅé¤Î¦ì¦V¿ï¾Ü©Êªº¬ã¨s(2/2)(Stereo-and Regioselectivity in Palladium-Catalyzed Allylic Amination by Direct Use of Allyl Alcohols)
|
2000/08/01 ~ 2001/07/31 |
26 |
088 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC 89-2113-M-037-005- ¡X 1 Ó¤H«¬
ª½±µ§Q¥Î²m¤þ¾JÃþ¤Æ¦Xª«¶i¦æÜj¶Ê¤Æ²m¤þ°òÓi¤Æ¤ÏÀ³ªº¥ßÅé¤Î¦ì¦V¿ï¾Ü©Êªº¬ã¨s(1/2)(Stereo-and Regioselectivity in Palladium-Catalyzed Allylic Amination by Direct Use of Allyl Alcohols)
|
1999/08/01 ~ 2000/07/31 |
27 |
087 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC88-2113-M037-015- ¡X 1 Ó¤H«¬
ª½±µ§Q¥Î²m¤þ¾JÃþ¤Æª«¶i¦æ¯Ò¶Ê¤Æ²m¤þ°ò¤Æ¤ÏÀ³¤§¬ã¨s(Palladium-catalyzed allylation by direct use of allyl alcohols)
|
1998/08/01 ~ 1999/07/31 |
28 |
086 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC87-2113-M037-004 ¡X
±qfÓi»Ä©M×ôÃþ¦X¦¨§t´á©M§t®ñÂøÀô¤Æ¦Xª«ªº¬ã¨s(Synthesis of nitrogen- and Oxygen-containing heterocycles from anilines and phenols)
|
1997/08/01 ~ 1998/07/31 |
29 |
085 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC86-2113-M037-004 ¡X
¸g¥ÑÖJ°òÜj¿ùÅ骺°Ñ»P¦X¦¨ÂøÀô¤Æ¦Xª«ªº¬ã¨s(Synthesis of heterocyclesw involving alkylpalladium complexes)
|
1996/08/01 ~ 1997/07/31 |
30 |
084 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC85-2113-M037-011 ¡X
´á-¤þ²m°ò-£\-²¸¤AñQ»Ïªº³¬Àô¤ÏÀ³(Cyclization of N-allyl-£\-thioacetamides)
|
1995/08/01 ~ 1996/07/31 |
31 |
083 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC84-2331-B037-090 ¡X
£_-Coniceine l¥Íª«ªº¦X¦¨¬ã¨s(Synthetic Studies on the £_-Coniceine Derivatives)
|
1994/08/01 ~ 1995/07/31 |
32 |
082 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC83-0208-M037-014 ¡X
¸g¥ÑÜj¶Ê¤Æ³¬Àô¤ÏÀ³¦X¦¨PyrolizidinesÃþ¤Æ¦Xª«ªº¬ã¨s(Synthesis of Pyrrolizidines via Palladium Catalyzed Cyclization)
|
1994/02/01 ~ 1995/07/31 |
33 |
081 ¡X K ¤¤¥¡°·«O§½ ¡X 81-P28-01 ¡X
§Q¥Î¾L»ÄÜj¶Ê¤Æ²mÓiÃþ¤Æ¦Xª«¶i¦æ¤À¤l¤º³¬Àô¤ÏÀ³¦X¦¨£^-carbolin-es ªº¬ã¨s(Intramolecular Cyclization of Enamines Involving Arylpalladium Comple- xes.Synthesis of £^-Carbolines)
|
1992/09/01 ~ 1995/08/31 |
34 |
081 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC82-0208-M037-014 ¡X
²mÓiÃþ¸g¥ÑªÚÜj¿ùÅ骺°Ñ»P¶i¦æ¤À¤l¤º³¬Àô¦X¦¨E-carbolinesªº¬ã¨s(Intramolecular Cyclization of Enamines Involoving Arylpalladium Complexes. Synthesis of £^-carbolines)
|
1993/02/01 ~ 1994/01/31 |
35 |
081 ¡X N °ê¬ì·|(ì¬ì§Þ³¡) ¡X NSC82-0412-B037-098-T ¡X
§Q¥Î¸K¤Æ¨È»É«P¶i²mÓiÃþÀô¤Æªº¬ã¨s(Copper(I) Iodide-Promoted Cyclization of Enamines)
|
1993/01/01 ~ 1993/12/31 |
Patent
NO | Patent Name | Country | Certified Date | Patent No |
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1 | 18£]¡Ð¥Ì¯ó¦¸»Äl¥Íª«¤Î¨ä¦X¦¨¤èªk | ¤¤µØ¥Á°ê | 2012/08/21 | I370821 |
2 | 18£]- ¥Ì¯ó¦¸»Äl¥Íª«¤Î¨ä¦X¦¨¤èªk | ¬ü°ê | 2012/12/11 | 8,329,940 |
3 | ºµªG»Äl¥Íª«¤Î¨äÂåÃIJզXª« | ¤¤µØ¥Á°ê | 2013/02/21 | I386415 |
4 | ºµªG»Äl¥Íª«¤Î¨äÂåÃIJզXª« | ¬ü°ê | 2014/05/20 | 8,729,055 |
5 | §@¥Î©ó·L¤pºÞ§ÜÀùÃĪ«¢±¡¦¡A¢´¡¦¡Ð¢ì¢ñ¢õ¢í¢ü¢ð¢÷£A£B¢ë¢ð¢é¢ô¢ë¢÷¢ö¢íl¥Íª«¤§¦X¦¨»P¬¡©Êµû¦ô | ¤¤µØ¥Á°ê | 2013/12/21 | I419687 |
6 | 18£]-¥Ì¯ó¦¸»Äl¥Íª«¤Î¨ä¥Î³~ | ¤¤µØ¥Á°ê | 2014/02/01 | I424839 |
7 | ¤@ºØ±þ¦ºÀù²ÓM¤§18£]-¥Ì¯ó¦¸»Äl¥Íª«¡B¨ä»s³Æ¤èªk¤Î¥]§t18£]-¥Ì¯ó¦¸»Äl¥Íª«¤§ÂåÃIJզXª« | ¬ü°ê | 2014/04/01 | 8,686,178 |
8 | 18£]- ¥Ì¯ó¦¸»Äl¥Íª«¤Î¨ä¦X¦¨¤èªk | ¬ü°ê | 2015/03/03 | 8,969,617 |
9 | 2-fÓi°ò-6-¥Ò°òf¦}?Ðül¥Íª«¤Î¨ä»s³Æ¤èªk»P¥Î³~ | ¤¤µØ¥Á°ê | 2016/08/01 | I543973 |