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The evolution of a stereoselective synthesis of the C1–C16 fragment of bryostatins. Matthew Ball, Anne Baron, Ben Bradshaw, Raphaël Dumeunier, Matthew O'Brien, Eric J. Thomas , Org. Biomol. Chem. , 2016 , 14 , 9650

Some limitations of an approach to the assembly of bryostatins by ring-closing metathesis. Raphaël Dumeunier, Thomas Gregson, Somhairle MacCormick, Hiroki Omori, Eric J. Thomas , Org. Biomol. Chem. , 2017 , 15 , 2768

Syntheses of C17–C27 fragments of 20-deoxybryostatins for assembly using Julia and metathesis reactions. Matthew Ball, Thomas Gregson, Hiroki Omori, Eric J. Thomas , Org. Biomol. Chem. , 2017 , 15 , 2740

Solution synthesis of homogeneous plate-like multifunctional CeO2 particles. Shu Yin, Yoshihiro Minamidate, Shunsuke Tonouchi, Takehiro Goto, Qiang Dong, Hisanori Yamane, Tsugio Sato , RSC Adv. , 2012 , 2 , 5976

Total syntheses of pamamycin 607 and methyl nonactate: stereoselective cyclisation of homoallylic alcohols that had been prepared with remote stereocontrol using allylstannanes. Olivier Germay, Naresh Kumar, Christopher G. Moore, Eric J. Thomas , Org. Biomol. Chem. , 2012 , 10 , 9709

2′-Fluoro-c-di-GMP as an oral vaccine adjuvant. Jia Li, Rhonda Kuo Lee, Wangxue Chen, Hongbin Yan , RSC Adv. , 2019 , 9 , 41481

In-water synthesis of isocyanides under micellar conditions. Francesca Brunelli, Silvio Aprile, Camilla Russo, Mariateresa Giustiniano, Gian Cesare Tron , Green Chem. , 2022 , 24 , 7022

No competitive inhibition of bicarbonate or carbonate for formate dehydrogenase from Candida boidinii-catalyzed CO2 reduction. Ryohei Sato, Yutaka Amao , New J. Chem. , 2022 , 46 , 15820

The synthesis of a series of adenosine A3 receptor agonists. Kenneth J. Broadley, Erica Burnell, Robin H. Davies, Alan T. L. Lee, Stephen Snee, Eric J. Thomas , Org. Biomol. Chem. , 2016 , 14 , 3765

94. o-Mercapto-azo-compounds. Part I. The coupling of tetrazotised 2 : 2′-diaminodiphenyl disulphide with β-naphthol. A. Burawoy, C. Turner , J. Chem. Soc. , 1950 , 469