Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jolicia F. Gauuan"'
Publikováno v:
Synlett. 2012:247-250
Autor:
Ying Zhai, Ellen Xia, Lei Chen, Bandarpalle B. Shankar, Qingbei Zeng, Anilkumar G. Nair, Sony Agrawal, Ronald N. Buckle, Guowei Zhou, Kannan P. Naicker, John P. Caldwell, Ling Tong, Yueheng Jiang, Stuart B. Rosenblum, Wensheng Yu, Kerry Keertikar, Haiqun Tang, Seong Heon Kim, Rong Liu, De-Yi Yang, Paul Ingravallo, Gregory Scott Martin, Samuel A. Vellekoop, Melissa L. Allard, Christian L. Holst, Michael P. Dwyer, Amin A. Nomeir, Robert Mazzola, Polivina Jolicia F Gauuan, Joseph A. Kozlowski, Oleg Selyutin, Rong Kong
Publikováno v:
Bioorganicmedicinal chemistry letters. 26(5)
HCV NS5A inhibitors have shown impressive in vitro potency profiles in HCV replicon assays thus making them attractive components for inclusion in an all oral fixed dose combination treatment regimen. Herein we describe the research efforts that led
Autor:
Matthew Robert Johnson, Rajesh A. Shenoy, Van-Duc Le, Jolicia F. Gauuan, Howard Roark, James M. Hamby, Cheng Guo, Peter R. Guzzo, Michael Stier, John E. Mangette
Publikováno v:
Synthetic Communications. 41:2769-2793
As part of a medicinal chemistry collaboration, a number of novel bi- and tricyclic α-amino acids were prepared through various routes and characterized by 1H nuclear Overhauser effect difference experiments. The syntheses provide a number of routes
Publikováno v:
The Journal of Organic Chemistry. 74:9546-9549
The asymmetric total synthesis of (+)-crassalactone D (4), a naturally occurring antitumor agent, has been achieved by employing an oxidative spirocyclization of furan 11 as the key step. Two close analogues, 7-epi-crassalactone D (14) and 5-epi-7-ep
Autor:
Paul E. Morin, Pancras C. Wong, Darren Orton, Wei Han, Patrick Y.S. Lam, Yun-Long Li, C.-H. Chang, Joseph M. Luettgen, Ruth R. Wexler, James R. Corte, Robert M. Knabb, Mark Hadden, Donald J. P. Pinto, Jolicia F. Gauuan, Zilun Hu, Xiang-Jun Jiang, Tianan Fang, Kan He, Daniel L. Cheney, Alan R. Rendina
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 18:2845-2849
Introduction of the phenyl piperidinone and phenyl pyridinone P4 moieties in the anthranilamide scaffold led to potent, selective, and orally bioavailable inhibitors of factor Xa. Anthranilamide 28 displayed comparable efficacy to apixaban in the rab
Autor:
Stephen B Bocckino, Brian J. Day, Michael P. Trova, Livia Gregor-Boros, Polivina Jolicia F Gauuan, James D. Crapo
Publikováno v:
Bioorganic & Medicinal Chemistry. 10:3013-3021
Carboxylic ester and amide-substituted analogues of [5,10,15,20-tetrakis(4-carboxyphenyl)-porphyrinato]manganese(III) chloride (MnTBAP) were synthesized and assayed as potential superoxide dismutase (SOD) mimetics. The tetraester analogues 4a and 4b
Publikováno v:
ChemInform. 43
A novel protocol is presented for the synthesis of benzimidazoles (III) which can be extended to benzoxazoles by use of 2-aminophenol.
Autor:
Jolicia F. Gauuan, Frank M. Hauser
Publikováno v:
ChemInform. 30
Autor:
Brian J. Day, Polivina Jolicia F Gauuan, Stephen M Bubb, Michael P. Trova, Stephen B Bocckino, Anthony D. Pechulis, James D. Crapo
Publikováno v:
Bioorganicmedicinal chemistry. 11(13)
Novel glyoxylate- and glyoxamide-derived metalloporphyrins 26-58 were synthesized and evaluated as potential superoxide dismutase (SOD) mimetics. Relative to previously studied MnTBAP analogues, the glyoxylate-derived metalloporphyrins 32, 39, and 54
Publikováno v:
Organic letters. 1(4)
[formula: see text] A regiospecific total synthesis of (+/-)-biphyscion (1) is described. A novel aspect of the plan was construction of the bianthraquinone ring system from a biphenyl intermediate through the use of a one-pot, double isobenzofuranon