Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Michael A. Ischay"'
Autor:
Michael A. Ischay, Brittanie Hoang, Dietrich P. Steinhuebel, Matthew R. Chin, Darryl D. Dixon, Danielle Elfgren, Lars Heumann, Willard Lew, Devon A. Mundal, Sean T. Neville, Nisha P. Shah, Bing Shi, Jonathan C. Tripp, Queenie Wang
Publikováno v:
Organic Process Research & Development. 26:2694-2706
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79acaa3d16f9a53bcd50e97f72bef21e
https://doi.org/10.1021/acs.oprd.2c00153
https://doi.org/10.1021/acs.oprd.2c00153
Autor:
Adam B. Weinstein, Michael A. Ischay, Edward M. Doerffler, Nolan D. Griggs, Greg T. Cizio, Matthew M. Logan, Lok Him Lawrence Yu, Baldip S. Kang, Dao Kathy, Patricia D. MacLeod
Publikováno v:
Organic Process Research & Development. 26:745-753
Non-alcoholic steatohepatitis (NASH) is a serious chronic liver disease characterized by progressive fibrosis that can lead to cirrhosis, liver failure, and death. Compound 1 is a farnesoid X recep...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1ef4c7eb06f8e503a2111b681956e1d
https://doi.org/10.1021/acs.oprd.1c00193
https://doi.org/10.1021/acs.oprd.1c00193
Publikováno v:
Synthesis. 45:2699-2705
We have developed a photocatalytic reduction of nitroarenes as an efficient, chemoselective route to biologically important N-phenyl hydroxamic acid scaffolds. Optimal conditions call for 2.5 mol% of a ruthenium photocatalyst, visible light irradiati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a443c2706d5a447947e3ab0cbbb1c0ef
https://doi.org/10.1055/s-0033-1338419
https://doi.org/10.1055/s-0033-1338419
Publikováno v:
Journal of the American Chemical Society. 135:2478-2481
Acid treatment of densely substituted 2-silyl-1,2-dihydropyridines provides a new and convenient entry to reactive azomethine ylides that can (1) be protonated and reduced with high stereoselectivity to give piperidines, (2) participate in [3 + 2] di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4977e60a963bb1c08fc5cd15edea82ee
https://doi.org/10.1021/ja312311k
https://doi.org/10.1021/ja312311k
Autor:
Michael A. Ischay, Tehshik P. Yoon
Publikováno v:
European Journal of Organic Chemistry. 2012:3359-3372
Organic reactions involving radical cation and radical anion intermediates are synthetically powerful umpolung processes that enable electronically mismatched couplings between pairs of electron-rich or pairs of electron-poor organic fragments. Never
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f28bedac0587e5ecda8b27e4e9f0e95
https://doi.org/10.1002/ejoc.201101071
https://doi.org/10.1002/ejoc.201101071
Publikováno v:
Journal of the American Chemical Society. 133:19350-19353
Ruthenium(II) polypyridyl complexes promote the efficient radical cation Diels-Alder cycloaddition of electron-rich dienophiles upon irradiation with visible light. These reactions enable facile [4 + 2] cycloadditions that would be electronically mis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e8f5d00437a7beeb4c90886a8e7e095
https://doi.org/10.1021/ja2093579
https://doi.org/10.1021/ja2093579
Publikováno v:
Nature Chemistry. 2:527-532
Light can be considered an ideal reagent for environmentally friendly, 'green' chemical synthesis; unlike many conventional reagents, light is non-toxic, generates no waste, and can be obtained from renewable sources. Nevertheless, the need for high-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84396b4efc285f51b9335d67ce3cd316
https://doi.org/10.1038/nchem.687
https://doi.org/10.1038/nchem.687
Publikováno v:
Journal of the American Chemical Society. 130:6610-6615
N-Sulfonyl oxaziridines are susceptible to electrophilic activation using copper(II) catalysts and react with styrenes under these conditions to provide 1,3-oxazolidines in a formal aminohydroxylation of the alkene. We propose a two-step mechanism in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d76c13e995f0ad55c9145eeb77a31892
https://doi.org/10.1021/ja800495r
https://doi.org/10.1021/ja800495r
Publikováno v:
European Journal of Organic Chemistry. 2007:5346-5352
Cyclic voltammetry and controlled-potential electrolysis were employed to study the catalytic reduction of five phenyl-conjugated haloalkynes by nickel(I) salen electrogenerated at carbon cathodes in dimethylformamide containing tetramethylammonium t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0efda9429f77ced63d2236fa8881d220
https://doi.org/10.1002/ejoc.200700655
https://doi.org/10.1002/ejoc.200700655
Autor:
Theodore B. Jennermann, Matthew P. Foley, Mohammad S. Mubarak, Michael A. Ischay, Dennis G. Peters, Philipp W. Raess, Krishnan Raghavachari
Publikováno v:
Journal of Electroanalytical Chemistry. 603:124-134
In dimethylformamide containing tetramethylammonium tetrafluoroborate, 1-iodooctane is reduced catalytically by nickel(I) salen electrogenerated at a glassy carbon cathode. Cyclic voltammograms for the nickel(II) salen–1-iodooctane system recorded
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b849f805f12e3903f0df5402c81b5929
https://doi.org/10.1016/j.jelechem.2007.01.025
https://doi.org/10.1016/j.jelechem.2007.01.025