Stephen Connon

Affiliations: 
2003- Trinity College, Dublin, Dublin, County Dublin, Ireland 
Area:
Synthetic organic chemistry, medicinal chemistry
Website:
http://chemistry.tcd.ie/staff/people/Connon/Stephen%20Connon.html
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Publications

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Smith SN, Trujillo C, Connon SJ. (2022) Catalytic, asymmetric azidations at carbonyls: achiral and -anhydride desymmetrisation affords enantioenriched γ-lactams. Organic & Biomolecular Chemistry
Litvajova M, Sorrentino E, Twamley B, et al. (2021) Base-free enantioselective S2 alkylation of 2-oxindoles via bifunctional phase-transfer catalysis. Beilstein Journal of Organic Chemistry. 17: 2287-2294
Cronin SA, Connon SJ. (2021) The kinetic resolution of oxazinones by alcoholysis: access to orthogonally protected β-amino acids. Organic & Biomolecular Chemistry. 19: 7348-7352
Delany EG, Connon SJ. (2020) Enantioselective N-heterocyclic carbene-catalysed intermolecular crossed benzoin condensations: improved catalyst design and the role of racemisation. Organic & Biomolecular Chemistry
Smith SN, Craig R, Connon SJ. (2020) Divergent Synthesis of γ-Amino Acid and γ-Lactam Derivatives from meso-Glutaric Anhydrides. Chemistry (Weinheim An Der Bergstrasse, Germany)
Maguire AC, Kumar V, Connon SJ. (2019) Highly chemoselective, sterically sensitive NHC-catalysed amine acylation with pyridil. Chemical Communications (Cambridge, England)
Lockett-Walters B, Trujillo C, Twamley B, et al. (2019) The base-catalysed Tamura cycloaddition reaction: calculation, mechanism, isolation of intermediates and asymmetric catalysis. Chemical Communications (Cambridge, England)
Connon S, Farid U, Aiello ML. (2019) Highly Enantioselective Catalytic Kinetic Resolution of α-Branched Aldehydes via Formal Cycloaddition with Homophthalic Anhydrides. Chemistry (Weinheim An Der Bergstrasse, Germany)
Collar AG, Trujillo C, Lockett-Walters B, et al. (2019) Catalytic Asymmetric γ-Lactam Synthesis from Enolisable Anhydrides and Imines. Chemistry (Weinheim An Der Bergstrasse, Germany)
Collar AG, Trujillo C, Connon SJ. (2019) Highly Enantio- and Diastereoselective Catalytic Asymmetric Tamura Cycloaddition Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany)
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