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• M. Nutter, H. Stone, M. Shipman, S. Roesner, Org. Biomol. Chem. 2024, DOI: 10.1039/d4ob00278d. ‘Stereoselective synthesis of (R)- and (S)-1,2-diazetidine-3-carboxylic acid derivatives for peptidomimetics’. [ 

• G. Saunders, S. Spring, E. Jayawant, I. Wilkening, S. Roesner, G. Clarkson, A. Dixon, R. Notman, M. Shipman, Chem. Eur. J. 2024, e202400308. ‘Synthesis and Functionalization of Azetidine-Containing Small Macrocyclic Peptides’. []

• R. Mohanrao, C. S. Pinto, A. Suchenko, G. J. Clarkson, M. Wills, S. Roesner, M. Shipman, M. K. Balasubramanian, ChemRxiv 2024, DOI:10.26434/chemrxiv-2024-s1fzw. ‘Single-benzene-based clickable fluorophores for in vitro and in vivo bioimaging’. ]

• S. Boswood, S. Roesner, Targets Heterocycl. Syst. 2023, 27, 1. ‘Methodologies for the Synthesis of β-Carbolines’. ]

• J. Kim, X. Ren, Y. Zhang, D. Fazzi, S. Manikandan, J. W. Andreasen, X. Sun, S. Ursel, H.-I. Un, S. Peralta, M. Xiao, J. Town, A. Marathianos, S. Roesner, T.-T. Bui, S. Ludwigs, H. Sirringhaus, S. Wang, Adv. Sci. 2023, 2303837. ‘Efficient N-type Organic Electrochemical Transistors and Field-effect Transistors based on PNDI-Copolymers Being Fluorinated Selenophene-Vinylene-Selenophenes’. ]

• G. J. Clarkson, S. Roesner, J. Org. Chem. 2023, 88, 684. ‘Synthesis of Benzofuropyridines and Dibenzofurans by a Metalation/Negishi Cross-Coupling/S_NAr Reaction Sequence’. ]

• S. Sathiyalingam, S. Roesner, Adv. Synth. Catal. 2022, 364, 1769. ‘Synthesis of α- and β-Carbolines by a Metalation/Negishi Cross-Coupling/S_NAr Reaction Sequence’. ]

• C. Dean, S. Roesner, S. Rajkumar, G. J. Clarkson, M. Jones, M.; Shipman, Tetrahedron 2021, 79, 131836. 'Synthesis of sp³-rich Chemical Libraries based upon 1,2-Diazetidines'. ]

• S. Roesner, J. D. Beadle, L. K. B. Tam, I. Wilkening, G. J. Clarkson, P. Raubo, M. Shipman, Org. Biomol. Chem. 2020, 18, 5400. 'Development of Oxetane Modified Building Blocks for Peptide Synthesis'. []

• C. Dean, R. Sundaram, S. Roesner, N. Carson, G. J. Clarkson, M. Wills, M. Jones, M. Shipman, Chem. Sci. 2020, 11, 1636. 'Readily accessible sp3-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality'. []

• S. Roesner, G. J. Saunders, I. Wilkening, E. Jayawant, J. V. Geden, P. Kerby, A. M. Dixon, R. Notman, M. Shipman, Chem. Sci. 2019, 10, 2465. ‘Macrocyclisation of Small Peptides Enabled by Oxetane Incorporation’. []

• A. Noble, S. Roesner, V. K. Aggarwal, Angew. Chem. Int. Ed. 2016, 55, 15920; Angew. Chem. 2016, 128, 16152. ‘Short Enantioselective Total Synthesis of Tatanan A and 3-epi-Tatanan A Using Assembly-Line Synthesis’. []

• S. Roesner, S. L. Buchwald, Angew. Chem. Int. Ed. 2016, 55, 10463; Angew. Chem. 2016, 128, 10619. ‘Continuous-Flow Synthesis of Biaryls by Negishi Cross-Coupling of Fluoro- and Trifluoromethyl-Substituted (Hetero)arenes’. []

• S. Roesner, D. J. Blair, V. K. Aggarwal, Chem. Sci. 2015, 6, 3718. ‘Enantioselective Installation of Adjacent Tertiary Benzylic Stereocentres by Using Lithiation–Borylation–Protodeboronation Methodology. Application to the Synthesis of Bifluranol and Fluorohexestrol’. []

• S. Roesner, C. A. Brown, M. Mohiti, A. P. Pulis, R. Rasappan, D. J. Blair, S. Essafi, D. Leonori, V. K. Aggarwal, Chem. Commun. 2014, 50, 4053. ‘Stereospecific Conversion of Alcohols into Pinacol Boronic Esters Using Lithiation‒Borylation Methodology with Pinacolborane’. []

• S. Roesner, V. K. Aggarwal, Can. J. Chem. 2012, 90, 965. ‘Enantioselective Synthesis of (R)-Tolterodine Using Lithiation/Borylation Methodology’. []

• S. Roesner, V. K. Aggarwal, Nature 2012, 487, 48. ‘Organic Chemistry ‒ Reactions at the End of a Tether’. ‘’ article.

• S. Roesner, J. M. Casatejada, T. G. Elford, R. P. Sonawane, V. K. Aggarwal, Org. Lett. 2011, 13, 5740. ‘Enantioselective Syntheses of (+)-Sertraline and (+)-Indatraline Using Lithiation/Borylation Methodology’. []

• S. Roesner, G. Hilt, Synthesis 2011, 662. ‘Substrate-Controlled Regioselective Cobalt(I)-Catalysed 1,4-Hydrovinylation Reactions’. []

• L. Kersten, S. Roesner, G. Hilt, Org. Lett. 2010, 12, 4920. ‘Synthesis and Characterization of Polycarbonyl Compounds via their BF2-Adducts’. []