Publications
Keith. G. Andrews: Google Scholar. ORCiD.
16. Programmable self-assembly for scalable molecular electronic architectures
Seham Helmi, Junjie Liu, Keith G Andrews, Robert Schreiber, Jonathan Bath, Harry L Anderson, Andrew J Turberfield, Arzhang Ardavan
2025-03-17 | Preprint
15. Enabling Next Generation Enzyme Mimics Through Local Electric Field Control in Organic Cage Catalysts
Marco Vitek; Igor Rončević*; Keith G. Andrews*
2025-07-04 | Preprint
14. Kinetic Analysis of the Redox-Neutral Catalytic Mitsunobu Reaction: Dehydration, Kinetic Barriers, and Hopping between Potential Energy Surfaces
Keith G. Andrews*; Stefan Borsley*
J. Am. Chem. Soc. 2025, 147, 21, 18240–18248
13. Beyond symmetric self-assembly and effective molarity: unlocking functional enzyme mimics with robust organic cages
Keith G. Andrews*
Beilstein J. Org. Chem. 2025, 21, 421–443
12. Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation
C. E. Shields; T. Fellowes; A. G. Slater; A. I. Cooper; K. G. Andrews*; F. T. Szczypiński*
Chem. Commun., 2024, 60, 6023-6026
11. Enzyme-like Acyl Transfer Catalysis in a Bifunctional Organic Cage
Keith G. Andrews*; Tomasz K. Piskorz; Peter N. Horton; Simon J. Coles
J. Am. Chem. Soc. 2024, 146, 26, 17887–17897
10. Programmable synthesis of organic cages with reduced symmetry
Keith G. Andrews*; Peter N. Horton; Simon J. Coles
Chem. Sci., 2024, 15, 6536-6543
9. Silyl Esters as Reactive Intermediates in Organic Synthesis
Marc J. Adler*; Melissa C. D’Amaral; Keith G. Andrews; Ross Denton*
Synthesis 2023, 55 (20), 3209-3238
8. Access to Amide‐Linked Organic Cages by in situ Trapping of Metastable Imine Assemblies: Solution Phase Bisamine Recognition
Keith G. Andrews*; Kirsten E. Christensen
Chem – Eur J 2023, 29 (26), e202300063
7. A practical catalytic reductive amination of carboxylic acids
Emma L. Stoll; Thomas Tongue; Keith G. Andrews; Damien Valette; David J. Hirst; Ross M. Denton*
Chem. Sci., 2020, 11, 9494-9500
6. Redox-neutral organocatalytic Mitsunobu reactions
Rhydian H. Beddoe; Keith G. Andrews; Valentin Magné; James D. Cuthbertson; Jan Saska; Andrew L. Shannon-Little; Stephen E. Shanahan; Helen F. Sneddon; Ross M. Denton*
Science, 2019, 365, 6456, 910-914
Impact:
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Buy our Mitsunobu catalyst here.
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In The Pipeline discussion of the Catalytic Mitsunobu reaction
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The sun never sets on synthetic methodology- redox neutral organocatalytic Mitsunobu reactions
5. A more critical role for silicon in the catalytic Staudinger amidation: silanes as non-innocent reductants
Keith G. Andrews; Ross M. Denton*
Chem. Commun., 2017, 53, 7982-7985
4. A practical and catalyst-free trifluoroethylation reaction of amines using trifluoroacetic acid
Keith G. Andrews; Radmila Faizova, Ross M. Denton*
Nat. Commun., 2017, 8, 15913
3. Catalytic reductive N-alkylation of amines using carboxylic acids
Keith G. Andrews; Declan M. Summers; Liam J. Donnelly; Ross M. Denton*
2. Improving the accuracy of computed 13C NMR shift predictions by specific environment error correction: fragment referencing
Keith G. Andrews; Alan C. Spivey*
1. Structural assignment of a bis-cyclopentenyl-β-cyanohydrin formed via alkene metathesis from either a triene or a tetraene precursor
Keith G. Andrews; C. S. Frampton; Alan C. Spivey*
Acta Cryst. C, 2013, 69, 1207-1211
