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Paul A. Clarke, Ph.D

Affiliations: 
1996-1999 Chemistry Florida State University, Tallahassee, FL, United States 
 1999-1999 Chemistry University of Exeter, Exeter, England, United Kingdom 
 1999-2006 Chemistry University of Nottingham, Nottingham, England, United Kingdom 
 2006- Chemistry University of York, York, England, United Kingdom 
Area:
Natural product synthesis
Website:
http://www.york.ac.uk/chemistry/staff/academic/a-c/pclarke/
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William Martin grad student 2001-2005 Nottingham
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Publications

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Maddocks CJ, Ermanis K, Clarke PA. (2020) Asymmetric "Clip-Cycle" Synthesis of Pyrrolidines and Spiropyrrolidines. Organic Letters
Hawkins K, Patterson A, Clarke PA, et al. (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
Vagkidis N, Brown AJ, Clarke PA. (2019) Evaluation of Amino Nitriles and an Amino Imidate as Organo­catalysts in Aldol Reactions Synthesis. 51: 4106-4112
Griggs SD, Thompson N, Tape DT, et al. (2018) Correction: Synthesis of highly substituted 2-spiropiperidines. Organic & Biomolecular Chemistry
Griggs SD, Thompson N, Tape DT, et al. (2018) Synthesis of highly substituted 2-spiropiperidines. Organic & Biomolecular Chemistry
Griggs SD, Tape DT, Clarke PA. (2018) Strategies for the synthesis of spiropiperidines - a review of the last 10 years. Organic & Biomolecular Chemistry
Steer AM, Bia N, Smith DK, et al. (2017) Prebiotic synthesis of 2-deoxy-d-ribose from interstellar building blocks promoted by amino esters or amino nitriles. Chemical Communications (Cambridge, England)
Griggs SD, Thompson N, Tape DT, et al. (2017) A Two-Step Synthesis of 2-Spiropiperidines. Chemistry (Weinheim An Der Bergstrasse, Germany)
Ermanis K, Hsiao YT, Kaya U, et al. (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. 8: 482-490
Clarke PA, Nasir NM, Sellars PB, et al. (2016) Synthesis of 2,6-trans- and 3,3,6-trisubstituted tetrahydropyran-4-ones from Maitland-Japp derived 2H-dihydropyran-4-ones: a total synthesis of diospongin B. Organic & Biomolecular Chemistry
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