Somhairle Maccormick

发表

Some limitations of an approach to the assembly of bryostatins by ring-closing metathesis.

E. J. Thomas, Raphael Dumeunier, Thomas J. Gregson, 2017, Organic & biomolecular chemistry.

Effective 1,5-, 1,6- and 1,7-remote stereocontrol in reactions of alkoxy- and hydroxy-substituted allylstannanes with aldehydes.

E. J. Thomas, J. S. Carey, S. Stanway, 2011, Organic & biomolecular chemistry.

Remote stereocontrol using (E)-6-hydroxy-4-methylhex-2-enyl(tri-n-butyl)stannane

E. J. Thomas, Somhairle Maccormick, 2006 .

A stereoselective synthesis of the C(1)–C(16) fragment of the bryostatins

E. J. Thomas, B. Bradshaw, A. Baron, 2004 .

A preliminary evaluation of a metathesis approach to bryostatins

E. J. Thomas, Raphael Dumeunier, B. Bradshaw, 2006 .

Synthesis and cellular uptake of carbamoylated mannose derivatives.

G. Veeneman, T. Boltje, H. Elferink, 2019, Carbohydrate research.

Discovery of potent and selective inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents.

P. Reaper, J. Pollard, M. Mortimore, 2011, Journal of medicinal chemistry.

Rational Design of 5-(4-(Isopropylsulfonyl)phenyl)-3-(3-(4-((methylamino)methyl)phenyl)isoxazol-5-yl)pyrazin-2-amine (VX-970, M6620): Optimization of Intra- and Intermolecular Polar Interactions of a New Ataxia Telangiectasia Mutated and Rad3-Related (ATR) Kinase Inhibitor.

P. Reaper, J. Golec, M. Griffiths, 2019, Journal of medicinal chemistry.

Selective killing of ATM- or p53-deficient cancer cells through inhibition of ATR.

P. Reaper, P. Charlton, J. Pollard, 2011, Nature chemical biology.

Discovery of potent and selective inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents.

P. Reaper, M. Mortimore, D. Kay, 2011, Journal of medicinal chemistry.