Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Magnus J. Johansson"'
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-11 (2024)
Abstract Catalysed C–H activation has emerged as a transformative platform for molecular synthesis and provides new opportunities in drug discovery by late-stage functionalisation (LSF) of complex molecules. Notably, small aliphatic motifs have gai
Externí odkaz:
https://doaj.org/article/708b3c8e318b499bbd388323ee8b4fa7
Autor:
Daniele Antermite, Stig D. Friis, Johan R. Johansson, Okky Dwichandra Putra, Lutz Ackermann, Magnus J. Johansson
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-12 (2023)
Abstract PROteolysis TArgeting Chimeras (PROTACs) are heterobifunctional molecules emerging as a powerful modality in drug discovery, with the potential to address outstanding medical challenges. However, the synthetic feasibility of PROTACs, and the
Externí odkaz:
https://doaj.org/article/018c82e0287d414f9caf142b4e057e8a
Autor:
Zhipeng Lin, Uttam Dhawa, Xiaoyan Hou, Max Surke, Binbin Yuan, Shu-Wen Li, Yan-Cheng Liou, Magnus J. Johansson, Li-Cheng Xu, Chen-Hang Chao, Xin Hong, Lutz Ackermann
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-8 (2023)
Abstract Electrooxidation has emerged as an increasingly viable platform in molecular syntheses that can avoid stoichiometric chemical redox agents. Despite major progress in electrochemical C−H activations, these arene functionalizations generally
Externí odkaz:
https://doaj.org/article/bdac31ddba7c44d8801256119bb301a1
Publikováno v:
iScience, Vol 24, Iss 5, Pp 102467- (2021)
Summary: Late-stage functionalization (LSF) has over the past years emerged as a powerful approach in the drug discovery process. At its best, it allows for rapid access to new analogues from a single drug-like molecule, bypassing the need for de nov
Externí odkaz:
https://doaj.org/article/c92a73b86d4b4f5c91d97ac885ddb370
Autor:
Daniele Antermite, Stig D. Friis, Johan R. Johansson, Okky D. Putra, Lutz Ackermann, Magnus J. Johansson
PROteolysis TArgeting Chimeras (PROTACs) are a powerful modality in drug discovery, offering the potential to address outstanding medical challenges. However, the synthetic feasibility of PROTACs, and the empiric and complex nature of their structure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7407f4ceba551c273af6fc4bdc96808e
https://doi.org/10.26434/chemrxiv-2023-669wc
https://doi.org/10.26434/chemrxiv-2023-669wc
Publikováno v:
JACS Au. 2:906-916
Herein, we report an iridium-catalyzed directed C-H amination methodology developed using a high-throughput experimentation (HTE)-based strategy, applicable for the needs of automated modern drug discovery. The informer library approach for investiga
Autor:
Simon Berritt, Melodie Christensen, Magnus J. Johansson, Shane W. Krska, Stephen G. Newman, Jessica Sampson, Eric M. Simmons, Ying Wang, Neil A. Strotman
Publikováno v:
ACS Symposium Series ISBN: 9780841297579
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e26ecbaa9ab79c6c65ee327dd320e8f3
https://doi.org/10.1021/bk-2022-1419.ch001
https://doi.org/10.1021/bk-2022-1419.ch001
Publikováno v:
The Power of High-Throughput Experimentation: Case Studies from Drug Discovery, Drug Development, and Catalyst Discovery (Volume 2) ISBN: 9780841297555
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d30a0b70619e99d9a6b59580cb62d4c4
https://doi.org/10.1021/bk-2022-1420.ch010
https://doi.org/10.1021/bk-2022-1420.ch010
Publikováno v:
Angewandte Chemie. 134
Autor:
Alejandro Valiente, Pablo Martínez‐Pardo, Gurpreet Kaur, Magnus J. Johansson, Belén Martín‐Matute
Publikováno v:
ChemSusChem. 15