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Dr. Stefan Roesner - Shipman Group

Stefan Roesner

Stefan Roesner received his Diploma in chemistry from Philipps-University Marburg, Germany in 2010. He moved to the UK and completed a PhD in organic chemistry with Prof. Varinder Aggarwal at the University of Bristol in 2014. After postdoctoral studies at the Massachusetts Institute of Technology under the supervision of Prof. Stephen Buchwald he returned in 2016 to the UK to become Senior Research Fellow in the Shipman group.

ORCID: 0000-0003-2143-4708

Email: S dot Roesner at warwick dot ac dot uk

Phone: +44(0)24 76 522758


• 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'. [Abstract]

• 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'. [Abstract]


• 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'. [Abstract]


• 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’. [Abstract]


• 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’. [Abstract]

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’. [Abstract]

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’. [Abstract]


• 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’. [Abstract]

tereospecific 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’. [Abstract]

Enantioselective synthesis of (R)-tolterodine using lithiation/borylation–protodeboronation methodology

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

Cover Nature

• 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’. [Abstract]

Enantioselective Syntheses of (+)-Sertraline and (+)-Indatraline Using Lithiation/Borylation–Protodeboronation Methodology

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

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’. [Abstract]

Synthesis and Characterization of Polycarbonyl Compounds via their BF2-Adducts