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- Comparison of six derivatizing agents for the determination of nine synthetic cathinones using gas chromatography-mass spectrometry. Khalid A. Alsenedi, Calum Morrison
, Anal. Methods
, 2017
, 9
, 2732
- 1,3-Dibromo-5,5-dimethylhydantoin (DBH) mediated one-pot syntheses of α-bromo/amino ketones from alkenes in water. Senhan Xu, Ping Wu, Wei Zhang
, Org. Biomol. Chem.
, 2016
, 14
, 11389
- Determination and quantitative analysis of designer drugs in human urine by liquid chromatography-mass spectrometry. Xueguo Chen, Ting Zhang
, Anal. Methods
, 2014
, 6
, 8291
- From linked open data to molecular interaction: studying selectivity trends for ligands of the human serotonin and dopamine transporter. Barbara Zdrazil, Eva Hellsberg, Michael Viereck, Gerhard F. Ecker
, Med. Chem. Commun.
, 2016
, 7
, 1819
- A copper(ii) bromide/NMO system for α-amination of esters under continuous-flow conditions with reduced catalyst loading. Yaman Chauhan, Kankanala Naveen Kumar, V. Ravichandiran, Sonali Bindita Jethy, Nirmala Mohanta, Sharada Prasanna Swain
, New J. Chem.
, 2024
, 48
, 6095
- Recent advances in the synthesis of α-amino ketones. Lewis A. T. Allen, Robert-Cristian Raclea, Philipp Natho, Philip J. Parsons
, Org. Biomol. Chem.
, 2021
, 19
, 498
- Water-based efficient alkyne transformation towards α-acetoxy/imido-ketones via oxidative coupling reactions using an alkylamine catalyst. Debasish Ghosh, Aniruddha Ganguly, Saikat Khamarui
, Org. Biomol. Chem.
, 2023
, 21
, 5225
- Determination of amphetamine-type stimulants (ATSs) and synthetic cathinones in urine using solid phase micro-extraction fibre tips and gas chromatography-mass spectrometry. Khalid A. Alsenedi, Calum Morrison
, Anal. Methods
, 2018
, 10
, 1431
- Decreasing the uncertainty of peak assignments for the analysis of synthetic cathinones using multi-dimensional ultra-high performance liquid chromatography. Cecilia M. Ochoa, Peter Shoenmakers, Claude R. Mallet, Ira S. Lurie
, Anal. Methods
, 2018
, 10
, 3178
- Isolation and structural determination of non-racemic tertiary cathinone derivatives. M.-J. Zhou, S. Bouazzaoui, L. E. Jones, P. Goodrich, S. E. J. Bell, G. N. Sheldrake, P. N. Horton, S. J. Coles, N. C. Fletcher
, Org. Biomol. Chem.
, 2015
, 13
, 9629