Zobrazeno 1 - 10
of 139
pro vyhledávání: '"Biing-Jiun Uang"'
Autor:
Shunsuke Kuribayashi, Tomoyuki Kurioka, Shinsuke Inagi, Ho-Jung Lu, Biing-Jiun Uang, Toshio Fuchigami
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 389-396 (2018)
We herein report that the regioselective anodic fluorination of S-alkyl benzothioate and its derivatives in various aprotic solvents using Et3N·nHF (n = 3–5) and Et4NF·nHF (n = 3–5) as supporting electrolyte and a fluorine source successfully p
Externí odkaz:
https://doaj.org/article/2a13d13f3b404b9da06ca51d26d50b9e
Autor:
Nutthawat Chuanopparat, Pondpavee Taweesak, Hsing Pang Hsieh, Phanida Thongaram, Adisak Thanetchaiyakup, Biing-Jiun Uang, Paiboon Ngernmeesri, Panitan Kraikruan
Publikováno v:
The Journal of Organic Chemistry. 86:1955-1963
In this work, we report a novel and simple one-pot synthesis of substituted dibenzo[b,f]oxepines under transition-metal-free conditions. This cascade process involves nucleophilic aromatic substitu...
Publikováno v:
Angewandte Chemie International Edition. 57:15572-15576
The first total synthesis of isopalhinine A, as well as unified syntheses of palhinine A and palhinine D, were successfully accomplished by means of a biomimetic strategy that proceeds through a bioinspired 5/6/6/9 tetracyclic intermediate, which mim
Publikováno v:
Angewandte Chemie. 130:15798-15802
Autor:
Pondpavee, Taweesak, Phanida, Thongaram, Panitan, Kraikruan, Adisak, Thanetchaiyakup, Nutthawat, Chuanopparat, Hsing-Pang, Hsieh, Biing-Jiun, Uang, Paiboon, Ngernmeesri
Publikováno v:
The Journal of organic chemistry. 86(2)
In this work, we report a novel and simple one-pot synthesis of substituted dibenzo[
Autor:
Ho-Jung Lu, Toshio Fuchigami, Tomoyuki Kurioka, Shunsuke Kuribayashi, Biing-Jiun Uang, Shinsuke Inagi
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 389-396 (2018)
We herein report that the regioselective anodic fluorination of S-alkyl benzothioate and its derivatives in various aprotic solvents using Et3N·nHF (n = 3–5) and Et4NF·nHF (n = 3–5) as supporting electrolyte and a fluorine source successfully p
Publikováno v:
Tetrahedron: Asymmetry. 28:803-808
A highly diastereoselective Michael-alkylation/oxidation methodology has been developed for the synthesis of optically active α-hydroxy-1,5-diester subunits. Inverse stereochemistry at the C2′ position could be achieved by using a Michael acceptor
Publikováno v:
Tetrahedron Letters. 58:706-710
Zn-catalyzed asymmetric alkylation reaction with carbonyl compounds has provided a straightforward method to access enantio-enriched tertiary alcohols. This chiral carbon-carbon bond forming process has attracted great attention in the field of asymm
Autor:
Hao-Chun Liao, Biing-Jiun Uang
Publikováno v:
Tetrahedron: Asymmetry. 28:105-109
Tofacitinib is an efficient and selective Janus kinase 3 (JAK3) inhibitor, and is used as an immunosuppressant drug for the treatment of rheumatoid arthritis and transplant patients. Herein we report a concise formal asymmetric synthesis of tofacitin
Autor:
John T.A. Hsu, Chun Hwa Chen, Hsing Pang Hsieh, Wen-Hsing Lin, Yih Shyan Lin, Biing-Jiun Uang, Chun Feng Chang, Wen Chieh Wang, Yi Yu Ke, Po Chu Kuo
Publikováno v:
European Journal of Medicinal Chemistry. 124:186-199
Aurora kinases have emerged as important anticancer targets so that there are several inhibitors have advanced into clinical study. Herein, we identified novel indazole derivatives as potent Aurora kinases inhibitors by utilizing in silico fragment-b