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William Unsworth
William Unsworth
Email confirmado em york.ac.uk
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Synthesis of spirocyclic indolenines
MJ James, P O'brien, RJK Taylor, WP Unsworth
Chemistry–A European Journal 22 (9), 2856-2881, 2016
3022016
Ring‐expansion reactions in the synthesis of macrocycles and medium‐sized rings
JR Donald, WP Unsworth
Chemistry–A European Journal 23 (37), 8780-8799, 2017
2642017
A happy medium: the synthesis of medicinally important medium-sized rings via ring expansion
AK Clarke, WP Unsworth
Chemical Science 11 (11), 2876-2881, 2020
1812020
Silver (I)‐or Copper (II)‐Mediated Dearomatization of Aromatic Ynones: Direct Access to Spirocyclic Scaffolds
MJ James, JD Cuthbertson, P O'brien, RJK Taylor, WP Unsworth
Angewandte Chemie International Edition 54 (26), 7640-7643, 2015
1632015
Phosphoranyl radical fragmentation reactions driven by photoredox catalysis
JA Rossi-Ashton, AK Clarke, WP Unsworth, RJK Taylor
ACS catalysis 10 (13), 7250-7261, 2020
1472020
Catalyst‐Driven Scaffold Diversity: Selective Synthesis of Spirocycles, Carbazoles and Quinolines from Indolyl Ynones
JTR Liddon, MJ James, AK Clarke, P O'brien, RJK Taylor, WP Unsworth
Chemistry–A European Journal 22 (26), 8777-8780, 2016
1372016
Silver (I)-catalyzed dearomatization of alkyne-tethered indoles: Divergent synthesis of spirocyclic indolenines and carbazoles
MJ James, RE Clubley, KY Palate, TJ Procter, AC Wyton, P O’brien, ...
Organic Letters 17 (17), 4372-4375, 2015
1292015
Silica‐Supported Silver Nitrate as a Highly Active Dearomatizing Spirocyclization Catalyst: Synergistic Alkyne Activation by Silver Nanoparticles and Silica
AK Clarke, MJ James, P O'brien, RJK Taylor, WP Unsworth
Angewandte Chemie 128 (44), 14002-14006, 2016
1142016
Direct imine acylation: rapid access to diverse heterocyclic scaffolds
WP Unsworth, C Kitsiou, RJK Taylor
Organic Letters 15 (2), 258-261, 2013
1122013
Visible-light-induced intramolecular charge transfer in the radical spirocyclisation of indole-tethered ynones
HE Ho, A Pagano, JA Rossi-Ashton, JR Donald, RG Epton, JC Churchill, ...
Chemical Science 11 (5), 1353-1360, 2020
1112020
Total synthesis of spirobacillene A
WP Unsworth, JD Cuthbertson, RJK Taylor
Organic Letters 15 (13), 3306-3309, 2013
1042013
The synthesis of structurally diverse macrocycles by successive ring expansion
C Kitsiou, JJ Hindes, P I'Anson, P Jackson, TC Wilson, EK Daly, ...
Angewandte Chemie International Edition 54 (52), 15794-15798, 2015
952015
A marine viral halogenase that iodinates diverse substrates
DS Gkotsi, H Ludewig, SV Sharma, JA Connolly, J Dhaliwal, Y Wang, ...
Nature chemistry 11 (12), 1091-1097, 2019
852019
Ring‐Expansion Approach to Medium‐Sized Lactams and Analysis of Their Medicinal Lead‐Like Properties
LG Baud, MA Manning, HL Arkless, TC Stephens, WP Unsworth
Chemistry–A European Journal 23 (9), 2225-2230, 2017
842017
Preparation and reactions of indoleninyl halides: scaffolds for the synthesis of spirocyclic indole derivatives
JTR Liddon, AK Clarke, RJK Taylor, WP Unsworth
Organic Letters 18 (24), 6328-6331, 2016
752016
Direct imine acylation for molecular diversity in heterocyclic synthesis
WP Unsworth, G Coulthard, C Kitsiou, RJK Taylor
The Journal of organic chemistry 79 (3), 1368-1376, 2014
732014
Direct imine acylation: Synthesis of the proposed structures of ‘upenamide
WP Unsworth, KA Gallagher, M Jean, JP Schmidt, LJ Diorazio, RJK Taylor
Organic letters 15 (2), 262-265, 2013
662013
Merging π-acid and Pd catalysis: Dearomatizing spirocyclization/cross-coupling cascade reactions of alkyne-tethered aromatics
HE Ho, TC Stephens, TJ Payne, P O’Brien, RJK Taylor, WP Unsworth
ACS Catalysis 9 (1), 504-510, 2018
632018
Internal Nucleophilic Catalyst Mediated Cyclisation/Ring Expansion Cascades for the Synthesis of Medium‐Sized Lactones and Lactams
A Lawer, JA Rossi‐Ashton, TC Stephens, BJ Challis, RG Epton, ...
Angewandte Chemie International Edition 58 (39), 13942-13947, 2019
622019
Selective Synthesis of Six Products from a Single Indolyl α‐Diazocarbonyl Precursor
MJ James, P O'brien, RJK Taylor, WP Unsworth
Angewandte Chemie International Edition 55 (33), 9671-9675, 2016
622016
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