Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ki Po Jang"'
Autor:
Christopher T. Check, C. Benjamin Schwamb, Karl A. Scheidt, David N. Barsoum, Ki Po Jang, Keegan P. Fitzpatrick
Publikováno v:
Organometallics. 39:2705-2712
Imidazol-2-ylidenes and their N,N′-diaryl derivatives constitute an important class of N-heterocyclic carbenes (NHCs) which possess a unique level of versatility in both organocatalysis and transition-metal catalysis. However, there remain few exam
Autor:
Christopher T. Check, Alex Wong, Karl A. Scheidt, C. Benjamin Schwamb, Michael H. Wang, Ki Po Jang
Publikováno v:
Angewandte Chemie. 127:4338-4342
Planar chirality remains an underutilized control element in asymmetric catalysis. Factors that have limited its broader application in catalysis include poor catalyst performance and difficulties associated with the economical production of enantiop
Autor:
Paul Ha-Yeon Cheong, Elizabeth O. McCusker, Ki Po Jang, Karl A. Scheidt, Gerri E. Hutson, Ryne C. Johnston
Publikováno v:
Journal of the American Chemical Society. 136:76-79
A highly selective NHC-catalyzed synthesis of γ-butyrolactones from the fusion of enals and α-ketophosphonates has been developed. Computational modeling of competing transition states was employed to guide a rational design strategy and achieve en
Autor:
Ki Po Jang, Christopher T. Check, Michael H. Wang, Karl A. Scheidt, Alex Wong, C. Benjamin Schwamb
Publikováno v:
ChemInform. 46
Planar chirality remains an underutilized control element in asymmetric catalysis. Factors that have limited its broader application in catalysis include poor catalyst performance and difficulties associated with the economical production of enantiop
Autor:
Ki Po Jang, Ryne C. Johnston, Gerri E. Hutson, Paul Ha-Yeon Cheong, Karl A. Scheidt, Elizabeth O. McCusker
Publikováno v:
ChemInform. 45
A highly selective NHC-catalyzed synthesis of γ-butyrolactones from the fusion of enals and α-ketophosphonates is reported.
Autor:
Dong Seok Jang, Hiyoung Kim, Heonjoong Kang, Seong Wook Na, Chan Hyuk Kim, Ki Po Jang, Eun Lee
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:2156-2158
Carbonyl ylide cycloaddition strategy was employed in the synthesis of platensimycin analogs. 7-Phenylplatensimycin and 11-methyl-7-phenylplatensimycin are more potent analogs of platensimycin.
Publikováno v:
Angewandte Chemie International Edition. 47:4009-4011
Autor:
Hiyoung Kim, Dong Seok Jang, Seong Wook Na, Eun Lee, Heonjoong Kang, Chan Hyuk Kim, Ki Po Jang
Publikováno v:
ChemInform. 41
Publikováno v:
ChemInform. 41
Isoplatensimycin, a novel analog of platensimycin, was synthesized via intramolecular dipolar cycloaddition of a carbonyl ylide. Isoplatensimycin showed little activities against strains of Staphylococcus aureus, but exhibited activities against some
Autor:
Eun Lee, Hiyoung Kim, Ki Po Jang, Dong Seok Jang, Heonjoong Kang, Seong Wook Na, Chan Hyuk Kim
Publikováno v:
Bioorganic & Medicinal Chemistry Letters.