Items where authors include "Clarke, Paul Andrew"

Article

Clarke, Paul Andrew orcid.org/0000-0003-3952-359X, Sosunovych, Bohdan and Brown, Alexander (2022) Amino Imidate-Catalyzed Asymmetric Michael Reactions of Ketones and Nitroalkenes. SynOpen. SO-2022-01-0005-OP.R1. pp. 67-74. ISSN 2509-9396

Clarke, Paul Andrew orcid.org/0000-0003-3952-359X, Alomari, Khadra, Chakravarthy, Sai Pavan et al. (2 more authors) (2022) Enantioselective “Clip-Cycle” Synthesis of Di-, Tri- and Spiro- Substituted Tetrahydropyrans. Organic and Biomolecular Chemistry. pp. 1181-1185. ISSN 1477-0520

Clarke, Paul Andrew orcid.org/0000-0003-3952-359X and Maddocks, Christopher (2021) Catalytic Asymmetric Total Syntheses of (R)-Bgugaine and (R)-Irnidine. Tetrahedron. 131789. pp. 1-9. ISSN 0040-4020

Clarke, Paul Andrew orcid.org/0000-0003-3952-359X, Ermanis, Kristaps and Maddocks, Christopher (2020) Asymmetric ‘Clip-Cycle’ Synthesis of Pyrrolidines and Spiropyrrolidines. Organic Letters. pp. 8116-8121. ISSN 1523-7052

Hawkins, Kirsten, Patterson, Anna, Clarke, Paul Andrew orcid.org/0000-0003-3952-359X et al. (1 more author) (2020) Catalytic Gels for a Prebiotically Relevant Asymmetric Aldol Reaction in Water : From Organocatalyst Design to Hydrogel Discovery and Back Again. Journal of the American Chemical Society. pp. 4379-4389. ISSN 1520-5126

Clarke, Paul Andrew orcid.org/0000-0003-3952-359X, Griggs, Samuel David, Thompson, Nathan et al. (2 more authors) (2018) Synthesis of highly substituted 2-spiropiperidines. Organic and Biomolecular Chemistry. pp. 6663-6674. ISSN 1477-0520

Clarke, Paul Andrew orcid.org/0000-0003-3952-359X, Smith, David Kelham orcid.org/0000-0002-9881-2714, Steer, Andrew Mark et al. (1 more author) (2017) Prebiotic Synthesis of 2-Deoxy-D-Ribose from Interstellar Building Blocks Promoted by Amino Esters or Amino Nitriles. Chemical Communications. c7cc06083a. pp. 10362-10365. ISSN 1364-548X

Clarke, Paul Andrew orcid.org/0000-0003-3952-359X, Ermanis, Kristaps, Hsiao, Yin-Ting et al. (2 more authors) (2017) The Stereodivergent Formation of 2,6-cis and 2,6-trans-Tetrahydropyrans: Experimental and Computational Investigation of the Mechanism of a Thioester Oxy-Michael Cyclization. Chemical Science. C6SC03478K. pp. 482-490. ISSN 2041-6539