Philip J. Parsons

Chemistry Imperial College, London, London, England, United Kingdom 
natural product synthesis
"Philip Parsons"

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Richard C. Cookson grad student 1978 University of Southampton
 (Some applications of sulphur in organic synthesis)
Gilbert Stork post-doc 1978-1979 Columbia
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Lee CF, Brown CE, Nielsen AJ, et al. (2022) A Stereocontrolled Total Synthesis of Lipoxin B4 and its Biological Activity as a Pro-Resolving Lipid Mediator of Neuroinflammation. Chemistry (Weinheim An Der Bergstrasse, Germany)
Mies T, White AJP, Parsons PJ, et al. (2020) Biomimetic Syntheses of Analogs of Hongoquercin A and B by Late-Stage Derivatization. The Journal of Organic Chemistry
Natho P, Rouse AB, Greenfield JL, et al. (2020) Regioselective synthesis of 1- and 4-tetralones from heteroaryl-3-cyclobutanols Tetrahedron. 76: 131636
Ma TK, Elliott DC, Reid S, et al. (2018) Meroterpenoid Synthesis via Sequential Polyketide Aromatization and Cationic Polyene Cyclization: Total Syntheses of (+)-Hongoquercin A and B and Related Meroterpenoids. The Journal of Organic Chemistry
Almond-Thynne J, White AJP, Polyzos A, et al. (2017) Synthesis and Reactions of Benzannulated Spiroaminals: Tetrahydrospirobiquinolines. Acs Omega. 2: 3241-3249
Stork G, Yamashita A, Hanson RM, et al. (2017) Synthetic Study toward Total Synthesis of (±)-Germine: Synthesis of (±)-4-Methylenegermine. Organic Letters
Parsons P, Allen L, Jones D, et al. (2017) Approaches to the Synthesis of Highly Substituted Aromatic and Fused Rings: Metal-Catalysed versus Thermal Cyclisation Synthesis. 50: 84-101
Elliott DC, Ma TK, Selmani A, et al. (2016) Sequential Ketene Generation from Dioxane-4,6-dione-keto-dioxinones for the Synthesis of Terpenoid Resorcylates. Organic Letters
Parsons PJ, Rushton SPG, Panta RR, et al. (2011) New synthetic routes to the kainoids: A synthesis of kainic acid and its analogues Tetrahedron. 67: 10267-10273
Parsons PJ, Board J, Faggiani D, et al. (2010) Model studies for the synthesis of the antibiotic lactonamycin and the discovery of new reactions and mechanisms for the construction of substituted heterocycles Tetrahedron. 66: 6526-6533
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