James D. Cuthbertson, PhD

2017- Chemistry University of Nottingham, Nottingham, England, United Kingdom 
Catalysis, heterocycle syntheses
"James Cuthbertson"
Mean distance: (not calculated yet)
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Beddoe RH, Andrews KG, Magné V, et al. (2019) Redox-neutral organocatalytic Mitsunobu reactions. Science (New York, N.Y.). 365: 910-914
Smalley AP, Cuthbertson JD, Gaunt MJ. (2017) Correction to "Palladium-Catalyzed Enantioselective C-H Activation of Aliphatic Amines Using Chiral Anionic BINOL-Phosphoric Acid Ligands". Journal of the American Chemical Society
Smalley AP, Cuthbertson JD, Gaunt MJ. (2017) Palladium-Catalyzed Enantioselective C-H Activation of Aliphatic Amines using Chiral Anionic BINOL-Phosphoric Acid Ligands. Journal of the American Chemical Society
Clarke AK, Liddon JT, Cuthbertson JD, et al. (2016) Dearomatisation approaches to spirocyclic dienones via the electrophilic activation of alkynes. Organic & Biomolecular Chemistry
Shaw MH, Shurtleff VW, Terrett JA, et al. (2016) Native functionality in triple catalytic cross-coupling: sp3 C-H bonds as latent nucleophiles. Science (New York, N.Y.)
Williamson AE, Ngouansavanh T, Pace RDM, et al. (2016) Rapid Generation of Complex Molecular Architectures by a Catalytic Enantioselective Dearomatization Strategy Synlett. 27: 116-120
Terrett JA, Cuthbertson JD, Shurtleff VW, et al. (2015) Switching on elusive organometallic mechanisms with photoredox catalysis. Nature. 524: 330-4
James MJ, Cuthbertson JD, O'Brien P, et al. (2015) Silver(I)- or Copper(II)-Mediated Dearomatization of Aromatic Ynones: Direct Access to Spirocyclic Scaffolds. Angewandte Chemie (International Ed. in English). 54: 7640-3
Cuthbertson JD, MacMillan DWC. (2015) The direct arylation of allylic sp3 C-H bonds via organic and photoredox catalysis Nature. 519: 74-77
Cuthbertson JD, Unsworth WP, Moody CL, et al. (2015) The total synthesis of (+)-elaeokanidine A: Natural product or isolation artefact? Tetrahedron Letters. 56: 3123-3126
See more...