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Journal of the American Chemical Society|December 24, 2014
The most reactive amide as a transition-state mimic for cis-trans interconversionIgor V Komarov, Stanislav Yanik, Aleksandr Yu Ishchenko, et al.
Chemical Research in Toxicology|December 9, 2020
Confidence in Inactive and Active Predictions from Structural AlertsAndrew J Wedlake, Timothy E H Allen, Jonathan M Goodman, et al.
Tuberculosis (Edinburgh, Scotland)|January 20, 2025
Microneedle-mediated intradermal delivery of Bacille Calmette-Guérin (BCG) vaccines for single-dose tuberculosis vaccinationSanha Lee, Taeyoon Kim, Keum-Yong Seong, et al.
Chemical Science|February 6, 2026
Oligomerisation and stereoselective polymerisation of alkenes and alkynes using pyridyl-based Al(iii) catalystsDipanjana Choudhury, Richard Danylyuk, Alexandros Terzopoulos, et al.
Chemical Communications (Cambridge, England)|October 30, 2009
The regioselective photochemical rearrangement of alpha-[PN(t)Bu](4)Henrike Bladt, Silvia Gonzalez Calera, Jonathan M Goodman, et al.
Environmental Science & Technology|May 21, 2020
In Silico Guidance for In Vitro Androgen and Glucocorticoid Receptor ToxCast AssaysTimothy E H Allen, Mark D Nelms, Stephen W Edwards, et al.
Molecules (Basel, Switzerland)|August 29, 2024
Correction: Samsuzzaman et al. A Synthetic Derivative SH 66 of Homoisoflavonoid from Liliaceae Exhibits Anti-Neuroinflammatory Activity against LPS-Induced Microglial Cells. Molecules 2024, 29, 3037Md Samsuzzaman, Lalita Subedi, Seong-Min Hong, et al.
Molecules (Basel, Switzerland)|July 13, 2024
A Synthetic Derivative SH 66 of Homoisoflavonoid from Liliaceae Exhibits Anti-Neuroinflammatory Activity against LPS-Induced Microglial CellsMd Samsuzzaman, Lalita Subedi, Seong-Min Hong, et al.
Chemical Science|June 14, 2021
Neural network activation similarity: a new measure to assist decision making in chemical toxicologyTimothy E H Allen, Andrew J Wedlake, Elena Gelžinytė, et al.
The Journal of Organic Chemistry|December 17, 2014
Base-mediated cascade rearrangements of aryl-substituted diallyl ethersJolene P Reid, Catherine A McAdam, Adam J S Johnston, et al.
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