Zobrazeno 1 - 10
of 60
pro vyhledávání: '"M. J. Kates"'
Autor:
J. H. Schauble, M. J. Kates
Publikováno v:
The Journal of Organic Chemistry. 61:4164-4167
Autor:
M. J. Kates, J. Herman Schauble
Publikováno v:
Journal of Heterocyclic Chemistry. 32:971-978
Reaction of five-membered ring anhydrides with sodium sulfide has previously been employed for synthesis of the corresponding thioanhydrides in low yields. Re-examination of the stoichiometry reveals reaction of cyclic anhydride with sodium sulfide (
Autor:
M. J. Kates, J. H. Schauble
Publikováno v:
ChemInform. 26
Autor:
J. H. Schauble, M. J. Kates
Publikováno v:
ChemInform. 27
Autor:
J. H. Schauble, M. J. Kates
Publikováno v:
ChemInform. 27
Autor:
M. J. Kates, J. Herman Schauble
Publikováno v:
The Journal of Organic Chemistry. 59:494-496
Autor:
Thomas J. Caggiano, John J. Fitzgerald, Thomas E. Christos, John M. Kulishoff, Michael L. McCaleb, Kurt E. Steiner, M. J. Kates, Robin Moore, Kenneth L. Kees
Publikováno v:
Journal of medicinal chemistry. 38(4)
Bioisosteric substitution was used as a tool to generate several new structural alternatives to the thiazolidine-2,4-dione and tetrazole heterocycles as potential antidiabetic agents. Among the initial leads that emerged from this strategy, a family
Autor:
Kenneth Keavey, Russell J. Thomas, Thomas McDonagh, Hamelin Estelle, Rory A. J. Curtis, Jonathan Barker, Peter S. DiStefano, Patricia Amouzegh, Jean-François Pons, Wei Tsung Yau, Andrew Napper, Jeffrey Hixon, M. J. Kates, Stephen Jones, Jeffrey O. Saunders, Manuel A. Navia, Adam Flegg
Publikováno v:
Journal of Medicinal Chemistry. 50:1086-1086
High-throughput screening against the human sirtuin SIRT1 led to the discovery of a series of indoles as potent inhibitors that are selective for SIRT1 over other deacetylases and NAD-processing enzymes. The most potent compounds described herein inh
Autor:
M. J. Kates, J. Herman Schauble
Publikováno v:
The Journal of Organic Chemistry. 60:6676-6677
Publikováno v:
Nursing Open; Sep2024, Vol. 11 Issue 9, p1-11, 11p