{"id":21,"date":"2021-10-24T19:42:06","date_gmt":"2021-10-24T18:42:06","guid":{"rendered":"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/?page_id=21"},"modified":"2026-01-15T15:55:08","modified_gmt":"2026-01-15T15:55:08","slug":"publications","status":"publish","type":"page","link":"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n<p><\/p>\n\n\n\n<p><\/p>\n\n\n\n<p><strong>33. Mechanochemical synthesis of organosodium compounds through direct sodiation of organic halides<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"767\" height=\"388\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/12\/image.png\" alt=\"\" class=\"wp-image-251\" style=\"width:463px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/12\/image.png 767w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/12\/image-300x152.png 300w\" sizes=\"auto, (max-width: 767px) 89vw, (max-width: 1000px) 54vw, (max-width: 1071px) 543px, 580px\" \/><\/figure>\n\n\n\n<p>Keisuke Kondo, Matthew E. Lowe, Nathan Davison, Paul G. Waddell, Roly J. Armstrong,* Erli Lu,* Koji Kubota,* Hajime Ito*<\/p>\n\n\n\n<p><em>Nature Synthesis<\/em>, <strong>2025<\/strong>, ASAP<\/p>\n\n\n\n<p>(<a href=\"https:\/\/www.nature.com\/articles\/s44160-025-00949-7\">DOI: 10.1038\/s44160-025-00949-7<\/a>)<\/p>\n\n\n\n<p>Highlighted in <a href=\"https:\/\/www.chemistryworld.com\/news\/ball-milled-sodium-provides-easy-access-to-organometallic-reagent\/4022713.article\">Chemistry World<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>32. A Reductive Mechanochemical Approach Enabling Direct Upcycling of Fluoride from Polytetrafluoroethylene (PTFE) into Fine Chemicals<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"166\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/10\/image-4.png\" alt=\"\" class=\"wp-image-239\" style=\"width:453px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/10\/image-4.png 500w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/10\/image-4-300x100.png 300w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/><\/figure>\n\n\n\n<p>Matthew E. Lowe, Benjamin M. Gallant, Nathan Davison, Matthew N. Hopkinson, Dominik J. Kubicki,<strong>*<\/strong> Erli Lu,<strong>*<\/strong> Roly J. Armstrong<strong>*<\/strong><\/p>\n\n\n\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2025<\/strong>, 1<em>47<\/em>, 40895<\/p>\n\n\n\n<p>(<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.5c14052\">DOI: 10.1021\/jacs.5c14052<\/a>)<\/p>\n\n\n\n<p>Highlighted in <a href=\"https:\/\/cen.acs.org\/materials\/polymers\/reaction-turns-teflon-toothpastes-key\/103\/web\/2025\/10\">C&amp;EN<\/a> and <a href=\"https:\/\/www.chemistryworld.com\/news\/mechanochemical-upcycling-of-teflon-creates-valuable-fluorinated-molecules\/4022410.article\">Chemistry World<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>31. Red-Shifted Circularly Polarised Luminescence from Helically Chiral&nbsp;<em>N<\/em>,<em>N<\/em>,<em>O<\/em>,<em>O<\/em>-Boron Chelated Dipyrromethenes through Synthetically Facile&nbsp;<em>meso<\/em>-CF<sub>3<\/sub>&nbsp;Modification<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"534\" height=\"253\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/12\/image-2.png\" alt=\"\" class=\"wp-image-257\" style=\"width:449px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/12\/image-2.png 534w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/12\/image-2-300x142.png 300w\" sizes=\"auto, (max-width: 534px) 100vw, 534px\" \/><\/figure>\n\n\n\n<p>Aminah A.&nbsp;Almarshad,&nbsp;Paul G.&nbsp;Waddell,&nbsp;Casey&nbsp;Dixon,&nbsp;Aaron D.G.&nbsp;Campbell,&nbsp;Roly J.&nbsp;Armstrong,&nbsp;Dmitry I.&nbsp;Levshov,&nbsp;Wouter A.&nbsp;Herrebout,&nbsp;Thomas J.&nbsp;Penfold,&nbsp;Dominic J.&nbsp;Black,&nbsp;Robert&nbsp;Pal,&nbsp;Santiago de la&nbsp;Moya,*&nbsp;Julian G.&nbsp;Knight,*&nbsp;Michael J.&nbsp;Hall*<\/p>\n\n\n\n<p><em>Dyes and Pigments<\/em>, <strong>2025<\/strong>, ASAP<\/p>\n\n\n\n<p><a href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0143720825008642\">(DOI: 10.1016\/j.dyepig.2025.113494)<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>30. Non-aqueous separation of lithium and sodium perchlorates by selective coordination with a hexadentate semi-flexible amine ligand<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"408\" height=\"215\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/12\/image-1.png\" alt=\"\" class=\"wp-image-254\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/12\/image-1.png 408w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/12\/image-1-300x158.png 300w\" sizes=\"auto, (max-width: 408px) 100vw, 408px\" \/><\/figure>\n\n\n\n<p>Jack M. Hemingway,* Xiao Yang, Paul G. Waddell, Joel Cornelio, Matthew E. Lowe, James A. Dawson, Peter R. Slater, Roly J. Armstrong, Erli Lu*<\/p>\n\n\n\n<p><em>Inorg. Chem. Front.<\/em>, <strong>2025<\/strong>, ASAP<\/p>\n\n\n\n<p><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/qi\/d5qi01799h\">(DOI: 10.1039\/D5QI01799H)<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>29. A Multicomponent Approach for the Stereoselective Synthesis of Atropisomeric N\u2013N Peptide Analogues<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"366\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/10\/image-1-1024x366.png\" alt=\"\" class=\"wp-image-232\" style=\"width:454px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/10\/image-1-1024x366.png 1024w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/10\/image-1-300x107.png 300w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/10\/image-1-768x274.png 768w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/10\/image-1.png 1030w\" sizes=\"auto, (max-width: 767px) 89vw, (max-width: 1000px) 54vw, (max-width: 1071px) 543px, 580px\" \/><\/figure>\n\n\n\n<p>Natalie J. Roper,&nbsp;George M. Hardy,&nbsp;Jack M. Wootton,&nbsp;Paul G. Waddell,&nbsp;James Wilson,&nbsp;&nbsp;Roly J. Armstrong&nbsp;*<\/p>\n\n\n\n<p><em>Chem. Commun.<\/em> <strong>2025<\/strong>, <em>61<\/em>, 17388<\/p>\n\n\n\n<p><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/cc\/d5cc05091j\" data-type=\"link\" data-id=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/cc\/d5cc05091j\" target=\"_blank\" rel=\"noreferrer noopener\">(DOI: 10.1039\/D5CC05091J)<\/a><\/p>\n\n\n\n<p>Highlighted in <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2739-0342\">Synfacts<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>28. C=O Methylenation mediated by organo-alkali metal reagents:<br>metal identity and ligand effects<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"483\" height=\"141\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/05\/image.png\" alt=\"\" class=\"wp-image-218\" \/><\/figure>\n\n\n\n<p>Xiao Yang, Nathan Davison,* Matthew E. Lowe, Paul G. Waddell, Roly J. Armstrong,* Claire L. McMullin,* Matthew N. Hopkinson, Erli Lu*<\/p>\n\n\n\n<p><em>Chem. Sci. <\/em><strong>2025<\/strong>, <em>16<\/em>, 11151 <\/p>\n\n\n\n<p>(<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/sc\/d5sc02313k\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/sc\/d5sc02313k<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>27. Double Click for Chirality: Chiral Dibenzo-cycloocta-bis-triazoles via Strain-Promoted Alkyne-Azide Cycloaddition<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"998\" height=\"295\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/03\/Graphical-Abstract.jpg\" alt=\"\" class=\"wp-image-210\" style=\"width:557px;height:auto\" \/><\/figure>\n\n\n\n<p>Sebastian Pim, Aaron D. G. Campbell, Dmitry Levshov, Wouter Herrebout, Gonzalo Dur\u00e1n-Sampedro, Michael J. Hall,*<em> <\/em>Roly J. Armstrong,* Donal F. O\u2019Shea*<\/p>\n\n\n\n<p><em>ChemPhotoChem<\/em>,<strong> 2025<\/strong>, <em>9<\/em>, e202500042 <\/p>\n\n\n\n<p>(<a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/cptc.202500042\">https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/cptc.202500042<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>26. CACHE Challenge #2: Targeting the RNA Site of the SARS-CoV-2 Helicase Nsp13<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"646\" height=\"436\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/03\/image.png\" alt=\"\" class=\"wp-image-205\" style=\"width:492px;height:auto\" \/><\/figure>\n\n\n\n<p><em>Journal of Chemical Information and Modeling<\/em>, <strong>2025<\/strong>, <em>65<\/em>, 6884 <\/p>\n\n\n\n<p>(<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jcim.5c00535\">https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jcim.5c00535<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>25. Stereoselective Synthesis of Atropisomeric Amides Enabled by Intramolecular Acyl Transfer<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"352\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2025\/01\/TOC-1.jpg\" alt=\"\" class=\"wp-image-192\" style=\"width:315px;height:auto\" \/><\/figure>\n\n\n\n<p>Jack Wootton, Natalie J. Roper, Catrin E. Morris, Victoria E. Maguire, Lee Duff, Paul G. Waddell, Adrian C. Whitwood, Richard Gammons, Afjal H Miah, Jason M. Lynam, Roly J. Armstrong,* William P. Unsworth*<\/p>\n\n\n\n<p><em>Chem. Sci.<\/em> <strong>2025<\/strong>, &nbsp;<em>16<\/em>, 3938 (<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/sc\/d4sc05760k\">https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/sc\/d4sc05760k<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>24. A Stereodivergent Multicomponent Approach for the Synthesis of C\u2013N Atropisomeric Peptide Analogues<\/strong><\/p>\n\n\n<\/p>\n<figure class=\"wp-block-image size-full is-resized\"><\/figure>\n<p><img loading=\"lazy\" decoding=\"async\" width=\"943\" height=\"369\" class=\"wp-image-168\" style=\"width: 550px\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2024\/09\/Graaphical-abstract.jpg\" alt=\"\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2024\/09\/Graaphical-abstract.jpg 943w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2024\/09\/Graaphical-abstract-300x117.jpg 300w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2024\/09\/Graaphical-abstract-768x301.jpg 768w\" sizes=\"auto, (max-width: 767px) 89vw, (max-width: 1000px) 54vw, (max-width: 1071px) 543px, 580px\" \/><\/p>\n\n\n<p>Natalie J. Roper, Aaron D. G. Campbell, Paul G. Waddell, Alistair K. Brown, Kristaps Ermanis,* Roly J. Armstrong*<\/p>\n\n\n\n<p><em>Chem. Sci.<\/em> <strong>2024<\/strong>, <em>15<\/em>, 16743 (<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/sc\/d4sc04700a\">https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/sc\/d4sc04700a<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>23. Synthesis, Structure and Stereodynamics of Atropisomeric N-Chloroamides<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"759\" height=\"292\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2024\/03\/Graphical-abstract.jpg\" alt=\"\" class=\"wp-image-160\" style=\"aspect-ratio:2.5968586387434556;width:441px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2024\/03\/Graphical-abstract.jpg 759w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2024\/03\/Graphical-abstract-300x115.jpg 300w\" sizes=\"auto, (max-width: 706px) 89vw, (max-width: 767px) 82vw, 740px\" \/><\/figure>\n\n\n\n<p>Aaron D. G. Campbell, Natalie J. Roper,<sup> <\/sup> Paul G. Waddell, Corinne Wills, Casey M. Dixon, Ross M. Denton, Kristaps Ermanis,* Roly J. Armstrong*<\/p>\n\n\n\n<p>Chem. Commun. <strong>2024<\/strong>, <em>60<\/em>, 3818 (<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/cc\/d4cc00268g\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/cc\/d4cc00268g<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>22. Interrogating the Configurational Stability of Atropisomers<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"275\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2023\/07\/image-1-1024x275.png\" alt=\"\" class=\"wp-image-138\" style=\"aspect-ratio:3.7222222222222223;width:613px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2023\/07\/image-1-1024x275.png 1024w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2023\/07\/image-1-300x81.png 300w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2023\/07\/image-1-768x207.png 768w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2023\/07\/image-1.png 1231w\" sizes=\"auto, (max-width: 767px) 89vw, (max-width: 1000px) 54vw, (max-width: 1071px) 543px, 580px\" \/><\/figure>\n\n\n\n<p>Jean-Paul Heeb, Jonathan Clayden,* Martin D. Smith,* Roly J. Armstrong*<\/p>\n\n\n\n<p><em>Nature Protocols,&nbsp;<\/em><strong><strong>2023<\/strong>, <\/strong><em>18<\/em>, 2745 (<a rel=\"noreferrer noopener\" href=\"https:\/\/www.nature.com\/articles\/s41596-023-00859-y\" target=\"_blank\">https:\/\/www.nature.com\/articles\/s41596-023-00859-y<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>21. Redox Reorganization: Aluminium Promoted 1,5-Hydride Shifts Allow the Controlled Synthesis of Multisubstituted Cyclohexenes<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"812\" height=\"199\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2023\/06\/image-1.png\" alt=\"\" class=\"wp-image-133\" style=\"aspect-ratio:4.087591240875913;width:546px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2023\/06\/image-1.png 812w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2023\/06\/image-1-300x74.png 300w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2023\/06\/image-1-768x188.png 768w\" sizes=\"auto, (max-width: 767px) 89vw, (max-width: 1000px) 54vw, (max-width: 1071px) 543px, 580px\" \/><\/figure>\n\n\n\n<p>Lewis B. Smith, Roly J. Armstrong, Jingyan Hou, Edward Smith, Ming Sze, Alistair J. Sterling, Alex Smith, Fernanda Duarte,* Timothy J. Donohoe*<\/p>\n\n\n\n<p><em> <em><em><em><em>Angew. Chem. Int. Ed<\/em><\/em><\/em><\/em><\/em>. <strong>2023<\/strong>, <em>62<\/em>, e202307424 (<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202307424\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202307424<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>20. Synthetic Strategies to Control C\u2013N Atropisomerism in Acyclic Amines and Amides<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"744\" height=\"412\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2023\/02\/Graphical-abstract.jpg\" alt=\"\" class=\"wp-image-125\" style=\"width:474px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2023\/02\/Graphical-abstract.jpg 744w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2023\/02\/Graphical-abstract-300x166.jpg 300w\" sizes=\"auto, (max-width: 706px) 89vw, (max-width: 767px) 82vw, 740px\" \/><\/figure><\/div>\n\n\n<p>Aaron D. G. Campbell, Roly J. Armstrong*<\/p>\n\n\n\n<p><em>Synthesis<\/em> <strong>2023<\/strong>, <em>55<\/em>, 2427. (DOI: <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2039-5424\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2039-5424<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>19. Pentamethylphenyl (Ph*) ketones: Unique building blocks for organic synthesis<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403921003609\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"155\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/1-s2.0-S0040403921003609-ga1.jpg\" alt=\"\" class=\"wp-image-99\" style=\"width:418px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/1-s2.0-S0040403921003609-ga1.jpg 500w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/1-s2.0-S0040403921003609-ga1-300x93.jpg 300w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/><\/a><\/figure><\/div>\n\n\n<p>Roly J. Armstrong,* Timothy J. Donohoe*<\/p>\n\n\n\n<p><em>Tetrahedron Lett.<\/em> <strong>2021<\/strong>, <em>74<\/em>, 153151 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403921003609\" target=\"_blank\">10.1016\/j.tetlet.2021.153151<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>18. Control of Absolute Stereochemistry in Transition-Metal-Catalyzed Hydrogen Borrowing Reactions<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/chem.202001253\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/1.-Chem.-Eur.-J.-2020-26-12912.jpg\" alt=\"\" class=\"wp-image-22\" \/><\/a><\/figure><\/div>\n\n\n<p>Timothy Kwok, Oskar Hoff, Roly J. Armstrong,* Timothy J. Donohoe*<\/p>\n\n\n\n<p><em>Chem. Eur. J.<\/em> <strong>2020<\/strong>,<em> 26<\/em>, 12912 (<a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/chem.202001253\" target=\"_blank\" rel=\"noreferrer noopener\">DOI: 10.1002\/chem.202001253<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>17. Enantioconvergent Alkylation of Ketones with Racemic Secondary Alcohols via Hydrogen Borrowing Catalysis<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2020\/cc\/d0cc00767f\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"489\" height=\"167\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/18.-Chem.-Commun.-2020-56-3543.png\" alt=\"\" class=\"wp-image-27\" style=\"width:433px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/18.-Chem.-Commun.-2020-56-3543.png 489w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/18.-Chem.-Commun.-2020-56-3543-300x102.png 300w\" sizes=\"auto, (max-width: 489px) 100vw, 489px\" \/><\/a><\/figure><\/div>\n\n\n<p>Daniella M. J. Cheang, Roly J. Armstrong, Wasim M. Akhtar, Timothy J. Donohoe*<\/p>\n\n\n\n<p><em><em>Chem. Commun<\/em><\/em>. <strong>2020<\/strong>, <em>56<\/em>, 3543 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/chem.202001253\" target=\"_blank\"><\/a><a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2020\/cc\/d0cc00767f\" target=\"_blank\">10.1039\/D0CC00767F<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>16. Chemo- and Regioselective Synthesis of Acyl-Cyclohexenes by a Tandem Acceptorless Dehydrogenation-[1,5]-Hydride Shift Cascade<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.9b12296?journalCode=jacsat&amp;quickLinkVolume=142&amp;quickLinkPage=2514&amp;selectedTab=citation&amp;volume=142\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"145\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/17.-J.-Am.-Chem.-Soc.-2020-142-2514.gif\" alt=\"\" class=\"wp-image-33\" style=\"width:426px;height:auto\" \/><\/a><\/figure><\/div>\n\n\n<p>Lewis B. Smith, Roly J. Armstrong, Daniel Matheau-Raven, Timothy J. Donohoe*<\/p>\n\n\n\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2020<\/strong>, <em>142<\/em>, 2514 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.9b12296?journalCode=jacsat&amp;quickLinkVolume=142&amp;quickLinkPage=2514&amp;selectedTab=citation&amp;volume=142\" target=\"_blank\">10.1021\/jacs.9b12296<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>15. A Hydrogen Borrowing Annulation Strategy for the Stereocontrolled Synthesis of Saturated Aza-Heterocycles<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2020\/cc\/d0cc00903b\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"477\" height=\"160\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/16.-Chem.-Commun.-2020-56-3563.png\" alt=\"\" class=\"wp-image-35\" style=\"width:391px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/16.-Chem.-Commun.-2020-56-3563.png 477w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/16.-Chem.-Commun.-2020-56-3563-300x101.png 300w\" sizes=\"auto, (max-width: 477px) 100vw, 477px\" \/><\/a><\/figure><\/div>\n\n\n<p>Anna E. R. Chamberlain, Kieran J. Paterson, Roly J. Armstrong, Heather C. Twin, Timothy J. Donohoe*<\/p>\n\n\n\n<p><em><em><em>Chem. Commun<\/em>. <\/em><\/em><strong>2020<\/strong>, <em>56<\/em>, 3563 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2020\/cc\/d0cc00903b\" target=\"_blank\">10.1039\/D0CC00903B<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>14. Synthesis of Allenes by 1,2-Elimination<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/www.eurekaselect.com\/176889\/article\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"706\" height=\"390\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/15.-Curr.-Org.-Chem.-2019-23-3027.-1.png\" alt=\"\" class=\"wp-image-39\" style=\"width:550px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/15.-Curr.-Org.-Chem.-2019-23-3027.-1.png 706w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/15.-Curr.-Org.-Chem.-2019-23-3027.-1-300x166.png 300w\" sizes=\"auto, (max-width: 706px) 100vw, 706px\" \/><\/a><\/figure><\/div>\n\n\n<p><\/p>\n\n\n\n<p>Roly J. Armstrong*<\/p>\n\n\n\n<p><em><em><em><em>Curr. Org. Chem<\/em>. <\/em><\/em><\/em><strong>2019<\/strong>, <em>23<\/em>, 3027 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/www.eurekaselect.com\/176889\/article\" target=\"_blank\"><\/a><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.2174\/1385272823666191121122011\" target=\"_blank\">10.2174\/1385272823666191121122011<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>13. Catalytic Asymmetric Synthesis of Cyclohexanes by Hydrogen Borrowing Annulations<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201907514\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"704\" height=\"214\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/14.-Angew.-Chem.-Int.-Ed.-2019-58-12558.jpg\" alt=\"\" class=\"wp-image-45\" style=\"width:450px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/14.-Angew.-Chem.-Int.-Ed.-2019-58-12558.jpg 704w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/14.-Angew.-Chem.-Int.-Ed.-2019-58-12558-300x91.jpg 300w\" sizes=\"auto, (max-width: 704px) 100vw, 704px\" \/><\/a><\/figure><\/div>\n\n\n<p>Roly J. Armstrong, Wasim M. Akhtar, Tom A. Young, Fernanda Duarte,* Timothy J. Donohoe*<\/p>\n\n\n\n<p><em><em><em><em>Angew. Chem. Int. Ed. <\/em><\/em><\/em><\/em><strong>2019<\/strong>, <em>58<\/em>, 12558 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201907514\" target=\"_blank\"><\/a><a href=\"https:\/\/doi.org\/10.1002\/anie.201907514\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/anie.201907514<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>12. Stereoselective Synthesis of Alicyclic Ketones: a Hydrogen Borrowing Approach<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402019310543\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"570\" height=\"144\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/13.-Tetrahedron-2019-130680.png\" alt=\"\" class=\"wp-image-47\" style=\"width:514px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/13.-Tetrahedron-2019-130680.png 570w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/13.-Tetrahedron-2019-130680-300x76.png 300w\" sizes=\"auto, (max-width: 570px) 100vw, 570px\" \/><\/a><\/figure><\/div>\n\n\n<p>Roly J. Armstrong, Wasim M. Akhtar, James R. Frost, Neil G. Stevenson, Timothy J. Donohoe*<\/p>\n\n\n\n<p><em><em><em>Tetrahedron<\/em><strong> <\/strong><\/em><\/em><strong>2019<\/strong>, <em>75<\/em>, 130680 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402019310543\" target=\"_blank\">10.1016\/j.tet.2019.130680<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>11. Stereoselective Synthesis of Cyclohexanes via an Iridium Catalyzed (5 + 1) Annulation Strategy<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.8b07776?journalCode=jacsat&amp;quickLinkVolume=140&amp;quickLinkPage=11916&amp;selectedTab=citation&amp;volume=140\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"150\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/12.-J.-Am.-Chem.-Soc.-2018-140-11916.gif\" alt=\"\" class=\"wp-image-48\" style=\"width:432px;height:auto\" \/><\/a><\/figure><\/div>\n\n\n<p>Wasim M. Akhtar, Roly J. Armstrong, James R. Frost, Neil G. Stevenson, Timothy J. Donohoe*<\/p>\n\n\n\n<p><em><em><em><em>J. Am. Chem. Soc.<\/em><strong> <\/strong><\/em><\/em><\/em><strong>2018<\/strong>, <em>140<\/em>, 11916 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.8b07776?journalCode=jacsat&amp;quickLinkVolume=140&amp;quickLinkPage=11916&amp;selectedTab=citation&amp;volume=140\" target=\"_blank\">10.1021\/jacs.8b07776<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>10. Enantiodivergent Synthesis of Allenes by Point to Axial Chirality Transfer<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201804446\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"432\" height=\"222\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/11.-Angew.-Chem.-Int.-Ed.-2018-57-8203-1.jpg\" alt=\"\" class=\"wp-image-54\" style=\"width:374px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/11.-Angew.-Chem.-Int.-Ed.-2018-57-8203-1.jpg 432w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/11.-Angew.-Chem.-Int.-Ed.-2018-57-8203-1-300x154.jpg 300w\" sizes=\"auto, (max-width: 432px) 100vw, 432px\" \/><\/a><\/figure><\/div>\n\n\n<p>Roly J. Armstrong, Meganathan Nandakumar, Rafael M. P. Dias, Adam Noble, Eddie L. Myers, Varinder K. Aggarwal*<\/p>\n\n\n\n<p><em><em><em><em>Angew. Chem. Int. Ed. <\/em><\/em><\/em><\/em><strong>2018<\/strong>, <em>57<\/em>, 8203 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/anie.201804446\" target=\"_blank\">10.1002\/anie.<\/a><a rel=\"noreferrer noopener\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201804446\" target=\"_blank\">201804446<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>9. 50 Years of Zweifel Olefination: a Transition-Metal-Free Coupling<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0036-1589046\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"600\" height=\"308\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/10.-Synthesis-2017-49-3323.gif\" alt=\"\" class=\"wp-image-56\" style=\"width:554px;height:auto\" \/><\/a><\/figure><\/div>\n\n\n<p>Roly J. Armstrong, Varinder K. Aggarwal*<\/p>\n\n\n\n<p><em><em><em><em><em>Synthesis<\/em><strong> <\/strong><\/em><\/em><\/em><\/em><strong>2017<\/strong>, <em>49<\/em>, 3323 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0036-1589046\" target=\"_blank\">10.1055\/s-0036-1589046<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>8. Stereodivergent Olefination of Enantioenriched Boronic Esters<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201610387\" target=\"_blank\" rel=\"noopener noreferrer\"><img decoding=\"async\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/9.-Angew.-Chem.-Int.-Ed.-2017-56-786.jpg\" alt=\"\" class=\"wp-image-58\" style=\"width:382px;height:auto\" \/><\/a><\/figure><\/div>\n\n\n<p>Roly J. Armstrong, Cristina Garc\u00eda-Ruiz, Eddie L. Myers, Varinder K. Aggarwal*<\/p>\n\n\n\n<p><em><em><em><em><em><em>Angew. Chem. Int. Ed. <\/em><\/em><\/em><\/em><\/em><\/em><strong>2017<\/strong>, <em>56<\/em>, 786 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201610387\" target=\"_blank\"><\/a><a href=\"https:\/\/doi.org\/10.1002\/anie.201610387\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/anie.201610387<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>7. Conjunctive Functionalization of Vinyl Boronate Complexes with Electrophiles: A Diastereoselective Three-Component Coupling<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2017\/cc\/c7cc01671a\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"486\" height=\"194\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/8.-Chem.-Commun.-2017-53-4922.png\" alt=\"\" class=\"wp-image-60\" style=\"width:444px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/8.-Chem.-Commun.-2017-53-4922.png 486w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/8.-Chem.-Commun.-2017-53-4922-300x120.png 300w\" sizes=\"auto, (max-width: 486px) 100vw, 486px\" \/><\/a><\/figure><\/div>\n\n\n<p>Roly J. Armstrong, Christopher Sandford, Cristina Garc\u00eda-Ruiz, Varinder K. Aggarwal*<\/p>\n\n\n\n<p><em>Chem. Commun.<\/em><strong> <\/strong><strong>2017<\/strong>, <em>53<\/em>, 4922 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2017\/cc\/c7cc01671a\" target=\"_blank\">10.1039\/C7CC01671A<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>6. Synthesis of Functionalized Alkenes by a Transition-Metal-Free Zweifel Coupling<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.7b01124?journalCode=orlef7&amp;quickLinkVolume=19&amp;quickLinkPage=2762&amp;selectedTab=citation&amp;volume=19\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"172\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/7.-Org.-Lett.-2017-19-2762.gif\" alt=\"\" class=\"wp-image-61\" style=\"width:432px;height:auto\" \/><\/a><\/figure><\/div>\n\n\n<p>Roly J. Armstrong, Worawat Niwetmarin, Varinder K. Aggarwal*<\/p>\n\n\n\n<p><em><em>Org. Lett.<\/em><strong> <\/strong><\/em><strong>2017<\/strong>, <em>19<\/em>, 2762 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.7b01124?journalCode=orlef7&amp;quickLinkVolume=19&amp;quickLinkPage=2762&amp;selectedTab=citation&amp;volume=19\" target=\"_blank\"><\/a><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/acs.orglett.7b01124\" target=\"_blank\">10.1021\/acs.orglett.7b01124<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>5. Homologation of Boronic Esters with Lithiated Epoxides<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"http:\/\/orgsyn.org\/demo.aspx?prep=v94p0234\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"590\" height=\"267\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/6.-Org.-Synth.-2017-94-234.png\" alt=\"\" class=\"wp-image-63\" style=\"width:476px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/6.-Org.-Synth.-2017-94-234.png 590w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/6.-Org.-Synth.-2017-94-234-300x136.png 300w\" sizes=\"auto, (max-width: 590px) 100vw, 590px\" \/><\/a><\/figure><\/div>\n\n\n<p>Roly J. Armstrong, Varinder K. Aggarwal*<\/p>\n\n\n\n<p><em>Org. Synth<\/em>. <strong>2017<\/strong>, <em>94<\/em>, 234 (<a rel=\"noreferrer noopener\" href=\"http:\/\/orgsyn.org\/demo.aspx?prep=v94p0234\" target=\"_blank\">DOI: 10.15227\/orgsyn.094.0234<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>4. Catalytic Enantioselective Synthesis of Atropisomeric Biaryls by a Cation-Directed O-Alkylation<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/www.nature.com\/articles\/nchem.2710\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"706\" height=\"128\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/5.-Nat.-Chem.-2017-9-558.png\" alt=\"\" class=\"wp-image-65\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/5.-Nat.-Chem.-2017-9-558.png 706w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/5.-Nat.-Chem.-2017-9-558-300x54.png 300w\" sizes=\"auto, (max-width: 706px) 100vw, 706px\" \/><\/a><\/figure><\/div>\n\n\n<p>John. D. Jolliffe, Roly. J. Armstrong, Martin. D. Smith*<\/p>\n\n\n\n<p><em>Nat. Chem<\/em>. <strong>2017<\/strong>, <em>9<\/em>, 558 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1038\/nchem.2710\" target=\"_blank\">10.1038\/nchem.2710<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>3. Cation-Directed Enantioselective N-Functionalization of Pyrroles<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0035-1560813\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"570\" height=\"176\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/4.-Synlett-2016-27-6.gif\" alt=\"\" class=\"wp-image-67\" \/><\/a><\/figure>\n\n\n\n<p>J. Armstrong, Melissa D\u2019Ascenzio, Martin D. Smith*<\/p>\n\n\n\n<p><em>Synlett<\/em><strong> 2016<\/strong>, <em>27<\/em>, 6 (DOI: <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0035-1560813\" target=\"_blank\" rel=\"noreferrer noopener\">10.1055\/s-0035-1560813<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>2. Catalytic Enantioselective Synthesis of Atropisomeric Biaryls: A Cation Directed Nucleophilic Aromatic Substitution Reaction<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.201408205\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"556\" height=\"140\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/3.-Angew.-Chem.-Int.-Ed.-2014-53-12822.jpg\" alt=\"\" class=\"wp-image-68\" style=\"width:456px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/3.-Angew.-Chem.-Int.-Ed.-2014-53-12822.jpg 556w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/3.-Angew.-Chem.-Int.-Ed.-2014-53-12822-300x76.jpg 300w\" sizes=\"auto, (max-width: 556px) 100vw, 556px\" \/><\/a><\/figure><\/div>\n\n\n<p>Roly J. Armstrong, Martin D. Smith*<\/p>\n\n\n\n<p><em>Angew. Chem. Int. Ed.<\/em><strong> 2014<\/strong>, <em>53<\/em>, 12822 (DOI: <a rel=\"noreferrer noopener\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.201408205\" target=\"_blank\">10.1002\/anie.201408205<\/a>)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-cyan-bluish-gray-color has-css-opacity has-cyan-bluish-gray-background-color has-background is-style-wide\" \/>\n\n\n\n<p><strong>1. <\/strong> <strong>Furanyl Cyclic Amines: a Diastereoselective Synthesis of 2,6-Syn-Disubstituted Piperidines Under Thermodynamic Control<\/strong><\/p>\n\n\n<div class=\"wp-block-image is-resized\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2012\/ob\/c2ob07008a\" target=\"_blank\" rel=\"noopener noreferrer\"><img loading=\"lazy\" decoding=\"async\" width=\"501\" height=\"192\" src=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/2.-Org.-Biomol.-Chem.-2012-10-2392.png\" alt=\"\" class=\"wp-image-70\" style=\"width:389px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/2.-Org.-Biomol.-Chem.-2012-10-2392.png 501w, https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/files\/2021\/10\/2.-Org.-Biomol.-Chem.-2012-10-2392-300x115.png 300w\" sizes=\"auto, (max-width: 501px) 100vw, 501px\" \/><\/a><\/figure><\/div>\n\n\n<p>Matthew O&#8217;Brien,* Andrew Leach, Roly J. Armstrong, Keting Chong, Ross Sheridan<\/p>\n\n\n\n<p><em>Org. Biomol. Chem<\/em>. <strong>2012<\/strong>, <em>10<\/em>, 2392 (DOI: <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2012\/ob\/c2ob07008a\" target=\"_blank\" rel=\"noreferrer noopener\">10.1039\/C2OB07008A<\/a>)<\/p>\n","protected":false},"excerpt":{"rendered":"<p>33. Mechanochemical synthesis of organosodium compounds through direct sodiation of organic halides Keisuke Kondo, Matthew E. Lowe, Nathan Davison, Paul G. Waddell, Roly J. Armstrong,* Erli Lu,* Koji Kubota,* Hajime Ito* Nature Synthesis, 2025, ASAP (DOI: 10.1038\/s44160-025-00949-7) Highlighted in Chemistry World 32. A Reductive Mechanochemical Approach Enabling Direct Upcycling of Fluoride from Polytetrafluoroethylene (PTFE) into &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/publications\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Publications&#8221;<\/span><\/a><\/p>\n","protected":false},"author":10502,"featured_media":0,"parent":0,"menu_order":4,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-21","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/wp-json\/wp\/v2\/pages\/21","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/wp-json\/wp\/v2\/users\/10502"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/wp-json\/wp\/v2\/comments?post=21"}],"version-history":[{"count":60,"href":"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/wp-json\/wp\/v2\/pages\/21\/revisions"}],"predecessor-version":[{"id":266,"href":"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/wp-json\/wp\/v2\/pages\/21\/revisions\/266"}],"wp:attachment":[{"href":"https:\/\/blogs.ncl.ac.uk\/rolyarmstrong\/wp-json\/wp\/v2\/media?parent=21"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}