Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kim S. Mühlfenzl"'
Publikováno v:
Mühlfenzl, K S, Sardana, M, Skrydstrup, T & Elmore, C S 2022, ' Visible-Light Enabled Late-Stage, Room-Temperature Aminocarbonylation of Aryl Iodides with Labeled Carbon Monoxide ', ChemistrySelect, vol. 7, no. 46, e202203582 . https://doi.org/10.1002/slct.202203582
In recent years, coupling reactions mediated by visible light have been widely studied because such reactions can often be run at significantly lower temperatures. In this work, aryl iodides were coupled with amines at ambient temperature in the pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeff371396898e863cc88166edacfbc8
https://pure.au.dk/portal/da/publications/visiblelight-enabled-latestage-roomtemperature-aminocarbonylation-of-aryl-iodides-with-labeled-carbon-monoxide(0149d200-5429-4a04-858e-f16d199a6e96).html
https://pure.au.dk/portal/da/publications/visiblelight-enabled-latestage-roomtemperature-aminocarbonylation-of-aryl-iodides-with-labeled-carbon-monoxide(0149d200-5429-4a04-858e-f16d199a6e96).html
Autor:
Kim S. Mühlfenzl, Mario Kendlbacher, David M. Barber, Christian Steinborn, Klaus Wurst, Thomas Magauer, Peter Mayer, Raphael E. Wildermuth
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Herein is given a full account of the evolution of the first total synthesis of (+)‐cornexistin. Initial efforts were based on masking the reactive maleic anhydride moiety as a 3,4‐substituted furan and on forming the nine‐membered carbocycle i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfc309d123506ea1c9f7a81017bdee0e
https://doi.org/10.1002/chem.202101849
https://doi.org/10.1002/chem.202101849
Autor:
Malvika Sardana, Kim S. Mühlfenzl, Sylvia T. M. Wenker, Christian Åkesson, Martin A. Hayes, Charles S. Elmore, Subhash Pithani
Publikováno v:
Journal of labelled compounds and radiopharmaceutricals
Cyclopropanes are commonly employed structural moieties in drug design since their incorporation is often associated with increased target affinity, improved metabolic stability, and increased rigidity to access bioactive conformations. Robust chemic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c291c57805272b77e1cc45c264467e9f