Zobrazeno 1 - 10
of 35
pro vyhledávání: '"N. Paul King"'
Autor:
Alan D. Borthwick, Marie Charbaut, Robert J. Young, Máire A. Convery, Ivan Leo Pinto, Andrew M. Mason, Weston Helen Elisabeth, Matthew Campbell, David W. Brown, Anthony J. Pateman, Henry Anderson Kelly, Derek Pollard, Shah Gita Punjabhai, John R. Toomey, N. Paul King, Stefan Senger, Eric Hortense, Ping Zhou, Hawa Diallo, Nigel S. Watson, Wendy R. Irving, Angela Patikis, Cynthia L. Burns-Kurtis, Savvas Kleanthous, Chuen Chan
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 18:28-33
Structure and property based drug design was exploited in the synthesis of sulfonamidopyrrolidin-2-one-based factor Xa (fXa) inhibitors, incorporating basic biaryl P4 groups, producing highly potent inhibitors with significant anticoagulant activitie
Publikováno v:
Angewandte Chemie International Edition. 44:618-621
Publikováno v:
Synthesis. :3279-3282
Furan-2-ylmethyl, thien-2-ylmethyl and pyrrol-2-ylmethyl tosylacetates undergo facile decarboxylative Claisen rearrangement upon exposure to N,O-bis(trimethylsilyl)acetamide-potassium acetate to yield the corresponding 2,3-disubstituted heteroaromati
Autor:
N. Paul King, Yun He, Dionisios Vourloumis, Frank Roschangar, Tianhu Li, Kyriacos C. Nicolaou
Publikováno v:
Angewandte Chemie International Edition. 37:84-87
Autor:
Frank Roschangar, N. Paul King, Tianhu Li, Dionisios Vourloumis, Yun He, Kyriacos C. Nicolaou
Publikováno v:
Angewandte Chemie. 110:89-92
Ringschlus durch Olefinmetathese (siehe unten, a), Abspaltung der Schutzgruppe (b), Stille-Kupplung (c) und die abschliesende Epoxidierung (d) sind die wesentlichen Schritte der ersten Totalsynthese des naturlich vorkommenden Epothilons E 1. Ausgehen
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1027-1038
We have identified a new class of catalysts for the asymmetric reduction of prochiral ketones by borane. Key to the architecture of effective catalysts is an N–PO structural unit which may be part of a phosphinamide, phosphonamide or a related stru
Autor:
S. Ninkovic, Kyriacos C. Nicolaou, Dionisios Vourloumis, F. Sarabia, N. Paul King, M. Ray V. Finlay, Yun He
Publikováno v:
Chemistry - A European Journal. 3:1971-1986
In order to probe structure-activity relationships in the epothilone area, two series of epothilone B analogues have been designed and synthesized. The first series containing an oxazole moiety in place of a thiazole on the side chain was constructed
Autor:
Frank Roschangar, Kyriacos C. Nicolaou, Hans Vallberg, Christopher G. Nicolaou, N. Paul King, Dionisios Vourloumis, Yun He
Publikováno v:
Chemistry - A European Journal. 3:1957-1970
For structure-activity relationship studies, two series of epothilone A (1) analogues have been designed and synthesized, one containing an oxazole moiety instead of the thiazole heterocycle and the other containing a spirocyclopropane moiety in plac
Autor:
M. Ray V. Finlay, Hans Vallberg, F. Sarabia, Pareskevi Giannakakou, Pascal Verdier-Pinard, Ernest Hamel, Joaquin Pastor, N. Paul King, Kyriacos C. Nicolaou, Nicolas Winssinger, S. Ninkovic, Dionisios Vourloumis, Frank Roschanger, Tianhu Li, Yun He
Publikováno v:
Angewandte Chemie. 109:2181-2187
Publikováno v:
Tetrahedron: Asymmetry. 5:801-804
A number of new catalysts for the asymmetric reductions of ketones by borane are described. The highest accelerations are achieved by catalysts in which the phosphinamide (R 2 NPO) unit can adopt a planar geometry. This observation has provided an in