Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Holly J, Davis"'
Autor:
Holly J. Davis, Thomas R. Ward
Publikováno v:
ACS Central Science, Vol 5, Iss 7, Pp 1120-1136 (2019)
Externí odkaz:
https://doaj.org/article/738ae7171d8044f3b61dd771245478d4
Publikováno v:
Chemcatchem
Through a rapid screening of Cp*Ir complexes based on a turn‐on type fluorescence readout, a [Cp*Ir(dipyrido[3,2‐a : 2’,3’‐c]phenazine)Cl]+ complex was found to catalyze the blue‐light promoted dehydrogenation of N‐heterocycles under ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01928c095888c6be8b808c4d8719ed48
https://doi.org/10.1002/cctc.202000488
https://doi.org/10.1002/cctc.202000488
Publikováno v:
Angewandte Chemie (International Ed. in English)
Selective functionalization at the meta position of arenes remains a significant challenge. In this work, we demonstrate that a single anionic bipyridine ligand bearing a remote sulfonate group enables selective iridium‐catalyzed borylation of a ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::282cd1dacad89ace790e9f67853267d7
https://doi.org/10.1002/anie.201708967
https://doi.org/10.1002/anie.201708967
Publikováno v:
Synthesis. 50:793-802
Herein, we give a full account of the development of the palladium-catalysed cross-coupling of benzylammonium salts with boronic acids. A range of benzylamine-derived quaternary ammonium salts can be coupled with boronic acids under relatively mild
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b8c7843a7df7d6fc6d5813dfef7cb93
https://doi.org/10.1055/s-0036-1588548
https://doi.org/10.1055/s-0036-1588548
Autor:
Robert J. Phipps, Holly J. Davis
Publikováno v:
Chemical Science
This perspective examines the progress that has been made in using non-covalent interactions to control regioselectivity and site-selectivity in catalysis.
Asymmetric catalysis has been revolutionised by the realisation that attractive non-coval
Asymmetric catalysis has been revolutionised by the realisation that attractive non-coval
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fabfe0209737fd5f7b0e133904038e2c
https://doi.org/10.1039/c6sc04157d
https://doi.org/10.1039/c6sc04157d
Publikováno v:
ChemCatChem. 12:4447-4447
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95da379cd310a3d819f5407ad4c43c42
https://doi.org/10.1002/cctc.202001353
https://doi.org/10.1002/cctc.202001353
Publikováno v:
Science (New York, N.Y.). 360(6387)
Basic heteroarenes are a ubiquitous feature of pharmaceuticals and bioactive molecules, and Minisci-type additions of radical nucleophiles are a leading method for their elaboration. Despite many Minisci-type protocols that result in the formation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ffa135a1d4d1d801a596c4fc0dddbbd4
https://pubmed.ncbi.nlm.nih.gov/29622723
https://pubmed.ncbi.nlm.nih.gov/29622723
Autor:
Sophie H. Gilbert, Madeline E. Kavanagh, Andrew W. Munro, Kirsty J. McLean, Chris Abell, Holly J. Davis, Janine L. Gray, Anthony G. Coyne
Publikováno v:
Chemmedchem
The cyclo‐dipeptide substrates of the essential M. tuberculosis (Mtb) enzyme CYP121 were deconstructed into their component fragments and screened against the enzyme. A number of hits were identified, one of which exhibited an unexpected inhibitor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16d0dc3ee3e0369d2a5c7fbc0af06a0d
https://pubmed.ncbi.nlm.nih.gov/27432475
https://pubmed.ncbi.nlm.nih.gov/27432475
Publikováno v:
Journal of the American Chemical Society. 138(39)
The use of noncovalent interactions to direct transition-metal catalysis is a potentially powerful yet relatively underexplored strategy, with most investigations thus far focusing on using hydrogen bonds as the controlling element. We have developed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1ca9ca09214c78f15a5d6be39defd8c5
https://pubmed.ncbi.nlm.nih.gov/27626468
https://pubmed.ncbi.nlm.nih.gov/27626468
The search for new scaffolds to complement current HTS and fragment libraries is an active area of research. The development of novel strategies to synthesise compounds with 3D character in order to expand the diversity of a fragment library was expl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48afc1dc5577652f6180d53685e1e345
https://www.repository.cam.ac.uk/handle/1810/256459
https://www.repository.cam.ac.uk/handle/1810/256459
