James D. Cuthbertson, PhD

Affiliations: 
2017- Chemistry University of Nottingham, Nottingham, England, United Kingdom 
Area:
Catalysis, heterocycle syntheses
Website:
https://thecuthbertsongroup.wixsite.com/thecuthbertsongroup/research
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"James Cuthbertson"
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Publications

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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
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