Staff Profile
I am a Lecturer in organic chemistry in the School of Natural and Environmental Sciences, Newcastle University. My research programme focusses on the development of new synthetic methodologies to tackle challenging problems in catalysis, synthesis, materials science and medicine. We are particularly interested in constructing new three-dimensional molecules, using catalysis to precisely tailor their three-dimensional shape and stereochemistry.
Before taking up this post, I held a Junior Research Fellowship at University College, University of Oxford. Prior to this, I worked as a Postdoctoral Research Associate with Prof. Timothy Donohoe (University of Oxford) and Prof. Varinder Aggarwal FRS (University of Bristol).
Qualifications:
2011-2015: DPhil in organic chemistry with Prof. Martin Smith (University of Oxford)
2007-2011: B.A. and MSci in Natural Sciences (University of Cambridge)
Links:
Scopus: click here
ORCID: click here
Our research programme broadly focuses on the development of new synthetic methodology to efficiently assemble organic molecules. We are particularly interested in using catalysis to control the shape and stereochemistry of these materials, enabling us to prepare a wide range of complex 3D structures that cannot be accessed using existing synthetic methods.
Current areas of interest include:
Asymmetric Catalysis
Catalysis plays a central role in society, enabling the production of important materials at low cost with minimal environmental impact. Our research is focussed on identifying new ways to control selectivity within catalytic reactions. This encompasses both the design of new ligands and catalyst systems, as well as the development of new catalytic asymmetric processes.
Non-classical 3D Materials
Drug discovery programmes are increasingly shifting their focus from sp2 molecules towards saturated, sp3-rich molecules which allow exploration of novel, three-dimensional biological and chemical space. We are exploring a complementary approach to this challenge, which involves creating three-dimensional materials by “repackaging” traditional 2D drug-like building blocks, connecting them together in unusual ways to generate novel 3D materials. These sp2-rich materials have a variety of exciting applications in drug development, as well as catalysis, materials science and nanotechnology.
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Articles
- Campbell ADG, Roper NJ, Waddell PG, Wills C, Dixon CM, Denton RM, Ermanis K, Armstrong RJ. Synthesis, Structure and Stereodynamics of Atropisomeric N‑Chloroamides. Chemical Communications 2024, 60(28), 3818-3821.
- Campbell ADG, Armstrong RJ. Synthetic Strategies to Control C–N Atropisomerism in Acyclic Amines and Amides. Synthesis 2023, 55.
- Smith LB, Armstrong RJ, Hou J, Smith E, Sze M, Sterling AJ, Smith A, Duarte F, Donohoe TJ. Redox Reorganization: Aluminium Promoted 1,5-Hydride Shifts Allow the Controlled Synthesis of Multisubstituted Cyclohexenes. Angewandte Chemie International Edition 2023, 62(36), e202307424.
- Heeb JP, Clayden J, Smith MD, Armstrong RJ. Interrogating the Configurational Stability of Atropisomers. Nature Protocols 2023, 18, 2745–2771.
- Armstrong RJ, Donohoe TJ. Pentamethylphenyl (Ph*) Ketones: Unique Building Blocks for Organic Synthesis. Tetrahedron Letters 2021, 74(22), 153151.
- Cheang DMJ, Armstrong RJ, Akhtar WM, Donohoe TJ. Enantioconvergent Alkylation of Ketones with Racemic Secondary Alcohols via Hydrogen Borrowing Catalysis. Chemical Communications 2020, 56, 3543-3546.
- Kwok T, Hoff O, Armstrong RJ, Donohoe TJ. Control of Absolute Stereochemistry in Transition-Metal-Catalysed Hydrogen-Borrowing Reactions. Chemistry: A European Journal 2020, 26(57), 12912-12926.
- Smith LB, Armstrong RJ, Matheau-Raven D, Donohoe TJ. Chemo- and Regioselective Synthesis of Acyl-Cyclohexenes by a Tandem Acceptorless Dehydrogenation-[1,5]-Hydride Shift Cascade. Journal of the American Chemical Society 2020, 142(5), 2514-2523.
- Chamberlain AER, Paterson KJ, Armstrong RJ, Twin HC, Donohoe TJ. A Hydrogen Borrowing Annulation Strategy for the Stereocontrolled Synthesis of Saturated Aza-Heterocycles. Chemical Communications 2020, 56(24), 3563-3566.
- Armstrong RJ. Synthesis of Allenes by 1,2-Elimination. Current Organic Chemistry 2019, 23(27), 3027-3039.
- Armstrong RJ, Akhtar WM, Frost JR, Christensen KE, Stevenson NG, Donohoe TJ. Stereoselective Synthesis of Alicyclic Ketones: A Hydrogen Borrowing Approach. Tetrahedron 2019, 75(48), 130680.
- Armstrong RJ, Akhtar WM, Young TA, Duarte F, Donohoe TJ. Catalytic Asymmetric Synthesis of Cyclohexanes by Hydrogen Borrowing Annulations. Angewandte Chemie International Edition 2019, 58(36), 12558-12562.
- Akhtar WM, Armstrong RJ, Frost JR, Stevenson NG, Donohoe TJ. Stereoselective Synthesis of Cyclohexanes via an Iridium Catalyzed (5 + 1) Annulation Strategy. Journal of the American Chemical Society 2018, 140(38), 11916–11920.
- Armstrong RJ, Aggarwal VK. Homologation of Boronic Esters with Lithiated Epoxides. Organic Syntheses 2018, 94, 234.
- Armstrong RJ, Nandakumar M, Dias RMP, Noble A, Myers EL, Aggarwal VK. Enantiodivergent Synthesis of Allenes by Point-to-Axial Chirality Transfer. Angewandte Chemie International Edition 2018, 57(27), 8203-8208.
- Armstrong RJ, Niwetmarin W, Aggarwal VK. Synthesis of Functionalized Alkenes by a Transition-Metal-Free Zweifel Coupling. Organic Letters 2017, 19(10), 2762-2765.
- Armstrong RJ, Garcia Ruiz C, Myers EL, Aggarwal VK. Stereodivergent Olefination of Enantioenriched Boronic Esters. Angewandte Chemie International Edition 2017, 56(3), 786-790.
- Armstrong RJ, Sandford C, Garcia Ruiz C, Aggarwal VK. Conjunctive Functionalization of Vinyl Boronate Complexes with Electrophiles: A Diastereoselective Three-Component Coupling. Chemical Communications 2017, 53(36), 4922-4925.
- Jolliffe JD, Armstrong RJ, Smith MD. Catalytic Enantioselective Synthesis of Atropisomeric Biaryls by a Cation-Directed O-Alkylation. Nature Chemistry 2017, 9, 558-562.
- Armstrong RJ, Aggarwal VK. 50 Years of Zweifel Olefination: A Transition-Metal-Free Coupling. Synthesis 2017, 49(15), 3323-3336.
- Armstrong RJ, DAscenzio M, Smith MD. Cation-Directed Enantioselective N-Functionalization of Pyrroles. Synlett 2016, 27(1), 6-10.
- Armstrong RJ, Smith MD. Catalytic Enantioselective Synthesis of Atropisomeric Biaryls: A Cation-Directed Nucleophilic Aromatic Substitution Reaction. Angewandte Chemie International Edition 2014, 53(47), 12822-12826.
- OBrien M, Leach A, Armstrong RJ, Chong K, Sheridan R. A Diastereoselective Synthesis of 2,6-Syn-Disubstituted Piperidines under Thermodynamic Control. Organic & Biomolecular Chemistry 2012, 10, 2392-2394.