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Nature Chemistry|September 24, 2013
End-to-end conformational communication through a synthetic purinergic receptor by ligand-induced helicity switchingRobert A Brown, Vincent Diemer, Simon J Webb, et al.Nature|June 22, 2022
De novo design of discrete, stable 310-helix peptide assembliesPrasun Kumar, Neil G Paterson, Jonathan Clayden, et al.Organic Letters|September 12, 2018
Polycyclic Indoline Derivatives by Dearomatizing Anionic Cyclization of Indole and Tryptamine-Derived UreasJessica E Hill, Quentin Lefebvre, Laura A Fraser, et al.Organic & Biomolecular Chemistry|May 17, 2014
Conformational analysis of helical aminoisobutyric acid (Aib) oligomers bearing C-terminal ester Schellman motifsSarah J Pike, James Raftery, Simon J Webb, et al.The Journal of Organic Chemistry|June 12, 2014
Atropisomerism about aryl-Csp(3) bonds: the electronic and steric influence of ortho-substituents on conformational exchange in cannabidiol and linderatin derivativesHatice Berber, Pedro Lameiras, Clément Denhez, et al.Chemical Communications (Cambridge, England)|February 26, 2011
A general synthetic approach to the amnesic shellfish toxins: total synthesis of (-)-isodomoic acid B, (-)-isodomoic acid E and (-)-isodomoic acid FGilles Lemière, Simon Sedehizadeh, Julie Toueg, et al.Organic Letters|April 17, 2013
Carbolithiation of S-alkenyl-N-aryl thiocarbamates: carbanion arylation in a connective route to tertiary thiolsDaniele Castagnolo, Daniel J Foley, Hatice Berber, et al.Nature Communications|May 8, 2023
Switching imidazole reactivity by dynamic control of tautomer state in an allosteric foldamerDavid P Tilly, Jean-Paul Heeb, Simon J Webb, et al.Organic Letters|December 18, 2019
An Aliphatic Bischler-Napieralski Reaction: Dihydropyridones by Cyclocarbonylation of 3-Allylimidazolidin-4-onesMostafa M Amer, Olatz Olaizola, Jennifer Carter, et al.Angewandte Chemie (International Ed. in English)|June 18, 2015
Pseudoephedrine-Directed Asymmetric α-Arylation of α-Amino Acid DerivativesRachel C Atkinson, Fernando Fernández-Nieto, Josep Mas Roselló, et al.Pageof 18