Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Madeleine C Deem"'
Autor:
Madeleine C. Deem, Joshua S. Derasp, Thomas C. Malig, Kea Legard, Curtis P. Berlinguette, Jason E. Hein
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-11 (2022)
The phenomenon of „ring-walking‟, wherein a metal catalyst remains bound to a pi system as it migrates to another coupling site, is supported largely by circumstantial evidence. Here the authors perform an in-depth kinetic study of Buchwald- Hart
Externí odkaz:
https://doaj.org/article/365c13a15c8b45108a75443d68976c01
Autor:
Madeleine C. Deem, Jason E. Hein
Publikováno v:
The Journal of Organic Chemistry. 88:1292-1297
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ea2d04e625fbb41cc1ce60b5a961ea8
https://doi.org/10.1021/acs.joc.2c02737
https://doi.org/10.1021/acs.joc.2c02737
Autor:
Madeleine C. Deem, Isabelle Cai, Joshua S. Derasp, Paloma L. Prieto, Yusuke Sato, Junliang Liu, Andrew J. Kukor, Jason E. Hein
Publikováno v:
ACS Catalysis. 13:1418-1430
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3ae4e04adda7b01234cbbd356b5cb2c
https://doi.org/10.1021/acscatal.2c05045
https://doi.org/10.1021/acscatal.2c05045
Autor:
Amanda Berg, Chelsea B Swartchick, Noah Forrest, Matthew Chavarria, Madeleine C Deem, Alyson N Sillin, Yuexin Li, Teresa M Riscoe, Aaron Nilsen, Michael K Riscoe, Warren JL Wood
Publikováno v:
Future Medicinal Chemistry. 14:1611-1620
Background: In 1948, the synthesis and Plasmodium lophurae activity of 2-hydroxy-1,4-naphthoquinones containing 3-alkyldiarylether side chains was reported. Method/results: The synthesis of five related compounds, designed to be more metabolically st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0b8277318d192f5b8c1e36d7e09f15b
https://doi.org/10.4155/fmc-2022-0127
https://doi.org/10.4155/fmc-2022-0127
Autor:
Matthew A. Larsen, Josep Saurí, Elisabeth Hennessy, Aaron Sather, Yu-hong Lam, Madeleine C. Deem
Publikováno v:
Journal of the American Chemical Society. 142:726-732
A new general de novo synthesis of pharmaceutically important N-(hetero)aryl piperidines is reported. This protocol uses a robustly diastereoselective reductive amination/aza-Michael reaction sequence to achieve rapid construction of complex polysubs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3d37d6c1c1977b2e93cd09cfc2cb543
https://doi.org/10.1021/jacs.9b13114
https://doi.org/10.1021/jacs.9b13114
Autor:
Josep Saurí, Aaron Sather, Elisabeth Hennessy, Madeleine C. Deem, Yu-hong Lam, Matthew A. Larsen
A new general de novo synthesis of pharmaceutically important N-(hetero)aryl piperidines is reported. This protocol uses a robustly diastereoselective reductive amination/aza-Michael reaction sequence to achieve rapid construction of complex polysubs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::154c1adb3fb8addedf3d277334bd02ab
https://doi.org/10.26434/chemrxiv.11317901.v1
https://doi.org/10.26434/chemrxiv.11317901.v1
