Zobrazeno 1 - 10
of 238
pro vyhledávání: '"David M. Lindsay"'
Autor:
Alison R. Cochrane, Alan R. Kennedy, William J. Kerr, David M. Lindsay, Marc Reid, Tell Tuttle
Publikováno v:
Catalysts, Vol 10, Iss 2, p 161 (2020)
A range of iridium(I) complexes of the type [Ir(cod)(NHC)PPh3)]X are reported, where the N-heterocyclic carbene (NHC) is derived from the naturally-occurring imidaozlium salt, Lepidiline A (1,3-dibenzyl-4,5-dimethylimidazolium chloride). A range of c
Externí odkaz:
https://doaj.org/article/959f54fd390c4048ac281ae574693871
Autor:
Jennifer Devlin, William. J. Kerr, David M. Lindsay, Timothy J. D. McCabe, Marc Reid, Tell Tuttle
Publikováno v:
Molecules, Vol 20, Iss 7, Pp 11676-11698 (2015)
Herein we report a combined experimental and theoretical study on the deuterium labelling of benzoate ester derivatives, utilizing our developed iridium N-heterocyclic carbene/phosphine catalysts. A range of benzoate esters were screened, including d
Externí odkaz:
https://doaj.org/article/c5ff85640cc8439ba15f2c120aa01ce5
Publikováno v:
Chemical Science.
A mechanistic study into the copper(I)-catalysed sulfonylative Suzuki-Miyaura reaction, incorporating sulfur dioxide, is described. Utilising spectroscopic and computational techniques, an exploration into the individual components of the competing c
Publikováno v:
Catalysis Science & Technology. 11:5498-5504
Herein we qualitatively examine the relationship between reaction rate and reaction selectivity in iridium-catalysed hydrogen isotope exchange (HIE) reactions directed by Lewis basic functional groups. We have recently developed a directing group sca
Autor:
Darren L. Poole, William J. Kerr, Blake J. M. Baker, David M. Lindsay, Vipulkumar Kantibhai Patel
Publikováno v:
Green Chemistry. 23:280-287
Described herein is a green, continuous flow process for the synthesis of various aminoimidazoheterocycles, through the Gröebke-Blackburn-Bienaymé reaction (GBBR). This multicomponent procedure combines aminoazines, aldehydes and isocyanides to gen
Autor:
Scott P. Runyon, Adele.E. Queen, Desong Zhong, David Hesk, David M. Lindsay, William J. Kerr, Timothy R. Fennell, Wayne Mascarella, Kenneth S. Rehder
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 63:196-202
[3 H]Genipin was synthesized in a single step by Ir(I) catalyzed hydrogen isotope exchange. Conditions for selective exchange of the sp2 CH bond ortho to the methyl ester functionality were developed through deuterium modeling studies through a catal
Autor:
William J. Kerr, David M. Lindsay
Publikováno v:
Cobalt Catalysis in Organic Synthesis
This chapter provides an overview of recent developments in the Pauson–Khand reaction. The work that is discussed herein is selected from the time period 2013–2018, and only cobalt‐mediated versions of the Pauson–Khand reaction are considered
Publikováno v:
Bonfield, H, Valette, D, Lindsay, D & Reid, M 2020, ' Stereoselective remote functionalization via palladium catalyzed redox-relay Heck methodologies ', Chemistry-A European Journal . https://doi.org/10.1002/chem.202002849
Chemistry (Weinheim an Der Bergstrasse, Germany)
Chemistry (Weinheim an Der Bergstrasse, Germany)
Exploration of novel, three‐dimensional chemical space is of growing interest in the drug discovery community and with this comes the challenge for synthetic chemists to devise new stereoselective methods to introduce chirality in a rapid and effic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bf8bd31da9476ada68db58aaa5a6c36
https://strathprints.strath.ac.uk/73551/7/Bonfield_etal_CEJ_2020_Stereoselective_remote_functionalization_via_palladium_catalyzed.pdf
https://strathprints.strath.ac.uk/73551/7/Bonfield_etal_CEJ_2020_Stereoselective_remote_functionalization_via_palladium_catalyzed.pdf
A palette of commonly used directing groups, including various pharmaceutically relevant nitrogen-containing heterocycles, are quantitatively ranked based on the results of intermolecular hydrogen isotope exchange competition reactions using two irid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcd74647ae1466b5a41da325678e61b9
https://strathprints.strath.ac.uk/73843/1/Timofeeva_etal_CST_2020_A_quantitative_empirical_directing_group_scale_for_selectivity.pdf
https://strathprints.strath.ac.uk/73843/1/Timofeeva_etal_CST_2020_A_quantitative_empirical_directing_group_scale_for_selectivity.pdf
Autor:
Adele E, Queen, David, Hesk, David M, Lindsay, William J, Kerr, Kenneth, Rehder, Tim, Fennell, Wayne, Mascarella, Desong, Zhong, Scott, Runyon
Publikováno v:
Journal of labelled compoundsradiopharmaceuticalsREFERENCES. 63(4)
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