Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Jay J, Dunsford"'
Autor:
Michael W. Fay, James Adams, Athanasios Angelis-Dimakis, Jason E. Camp, Jay J. Dunsford, Joshua Britton, Thomas W. Bousfield
Publikováno v:
Synthesis. 50:3862-3874
A dehydrative cross-coupling of 1-phenylethanol catalysed by sugar derived, in situ formed palladium(0) nanoparticles under acidic conditions is realised. The acidic conditions allow for use of alcohols as a feedstock in metal-mediated coupling react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7b5d0819845c3d6caf12b57ebbde034
https://doi.org/10.1055/s-0037-1610246
https://doi.org/10.1055/s-0037-1610246
Autor:
Michael J. Ingleson, Rachel J. Kahan, S. Endres, Iñigo J. Vitorica-Yrezabal, J. E. Jones, Andrew J. Warner, Jay J. Dunsford, Daniel L. Crossley, Jessica Cid, R. A. Smith
Publikováno v:
Chemical Science
Ingleson, M, Kahan, R, Endres, S, Warner, A, Smith, R, Cid, J, Dunsford, J, Jones, J & Vitorica-Yrezabal, I 2017, ' A Modular Route to Boron Doped PAHs by Combining Borylative Cyclisation and Electrophilic C-H Borylation. ', Chemical Science . https://doi.org/10.1039/C7SC02793A
Ingleson, M, Kahan, R, Endres, S, Warner, A, Smith, R, Cid, J, Dunsford, J, Jones, J & Vitorica-Yrezabal, I 2017, ' A Modular Route to Boron Doped PAHs by Combining Borylative Cyclisation and Electrophilic C-H Borylation. ', Chemical Science . https://doi.org/10.1039/C7SC02793A
Starting from simple alkynes, sequential borylative cyclisation/electrophilic C–H borylation represents a simple modular route to novel B-doped PAHs.
Heteroatom doping into polyaromatic hydrocarbons (PAHs) is a powerful approach for modifying
Heteroatom doping into polyaromatic hydrocarbons (PAHs) is a powerful approach for modifying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a46504a14e7015c815576e9efe3f5de
https://doi.org/10.1039/c7sc02793a
https://doi.org/10.1039/c7sc02793a
Autor:
Oliver S. G. Dacosta, Robert D.J. Smith, Joshua Britton, Rebecca K. Blundell, Thomas W. Bousfield, Jason E. Camp, James Adams, Michael W. Fay, Jay J. Dunsford
Publikováno v:
RSC Advances. 6:16115-16121
In situ-generated, glucose-derived palladium(0) nanoparticles were shown to be convenient and effective catalysts for aqueous Mizoroki–Heck, Sonogashira and Suzuki–Miyaura cross-coupling reactions. The addition of only 4–10 mol% glucose to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f86b41d456428ea1f1032de22200b53
https://doi.org/10.1039/c5ra25712c
https://doi.org/10.1039/c5ra25712c
Autor:
Daniel L, Crossley, Pakapol, Kulapichitr, James E, Radcliffe, Jay J, Dunsford, Inigo, Vitorica-Yrezabal, Rachel J, Kahan, Adam W, Woodward, Michael L, Turner, Joseph J W, McDouall, Michael J, Ingleson
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Benzothiadiazole (BT) directed C−H borylation using BCl3, followed by B−Cl hydrolysis and Suzuki–Miyaura cross‐coupling enables facile access to twisted donor–acceptor compounds. A subsequent second C−H borylation step provides, on arylat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9e5f345ab811cb0aaf1ca7be239d1ee8
https://pubmed.ncbi.nlm.nih.gov/29781115
https://pubmed.ncbi.nlm.nih.gov/29781115
Publikováno v:
Dunsford, J J, Clark, E R & Ingleson, M J 2015, ' Direct C(sp(2))-C(sp(3)) Cross-Coupling of Diaryl Zinc Reagents with Benzylic, Primary, Secondary, and Tertiary Alkyl Halides ', ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, vol. 54, no. 19, pp. 5688-5692 . https://doi.org/10.1002/anie.201411403
The direct C(sp2)-C(sp3) cross-coupling of diaryl zinc reagents with benzylic, primary, secondary, and tertiary alkyl halides proceeded in the absence of coordinating ethereal solvents at ambient temperature without the addition of a catalyst. The C(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f56e56cc4e472cf55593cceeb7a2b26
https://doi.org/10.1002/anie.201411403
https://doi.org/10.1002/anie.201411403
Autor:
Catrin Ffion Williams, Simon J. A. Pope, Simon J. Coles, Anthony Joseph Hayes, David Lloyd, Oliver J. Stacey, Jay J. Dunsford, Angelo James Amoroso, Peter N. Horton, James Alexis Platts
Publikováno v:
ResearcherID
A heterometallic, water soluble PtII–GdIII complex possesses visible luminescence and enhanced water relaxivity whilst showing promise and application in cell imaging studies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52961906398e9a1c78d9952918eb00b7
https://doi.org/10.1039/c5cc02623g
https://doi.org/10.1039/c5cc02623g
Ring-Expanded N-Heterocyclic Carbenes for Copper-Mediated Azide-Alkyne Click Cycloaddition Reactions
Autor:
Filip, Sebest, Jay J, Dunsford, Matthew, Adams, Jeremy, Pivot, Paul D, Newman, Silvia, Díez-González
Publikováno v:
Chemcatchem
A series of well‐defined copper(I) complexes bearing ring‐expanded N‐heterocyclic carbene (NHC) ligands has been applied to the azide–alkyne cycloaddition reaction. The obtained results notably showed that the six‐membered NHC ligands outpe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::776bde75f723305140c96568d83e062b
https://pubmed.ncbi.nlm.nih.gov/29861792
https://pubmed.ncbi.nlm.nih.gov/29861792
Publikováno v:
Organometallics
The relative (to BEt3) hydride ion affinity (HIA) of a series of acridine borenium salts has been calculated, with some HIAs found to be similar to that for [Ph3C]+. The HIA at the acridine C9 position is controlled by both acridine and the boron sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c29891454e857f830986d4ca03816624
https://pubmed.ncbi.nlm.nih.gov/29430073
https://pubmed.ncbi.nlm.nih.gov/29430073
Autor:
Jay J. Dunsford, Kingsley J. Cavell
Publikováno v:
Organometallics. 33:2902-2905
The synthesis and characterization of the new six- and seven-membered Pd–PEPPSI-type N-heterocyclic carbene (NHC) complexes 3 and 4 is described. Complexes of the general formula [Pd(NHC)(3ClPy)Cl2] (NHC = 6- or 7-Mes, 3ClPy = 3-chloropyridine) are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fff90ccf9fcf2b869de9cb50ef0a2e3
https://doi.org/10.1021/om5003107
https://doi.org/10.1021/om5003107
Publikováno v:
Organometallics. 33:370-377
(NHC)2FeCl2 complexes undergo methoxide transfer in preference to aryl transfer from [(Aryl)B(OR)3]−, while addition of ArylBY2 (Y = Cl, OR) to (NHC)Fe–methoxide compounds leads only to formation of (NHC)BY2Aryl. The addition of PhBCl2 to (NHC)2F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::067f3bc7198dacba8702f0e79716112b
https://doi.org/10.1021/om401105k
https://doi.org/10.1021/om401105k