Nigel Simpkins, Ph.D

Affiliations: 
Chemistry University of Birmingham, Birmingham, England, United Kingdom 
Area:
Organic chemistry
Website:
http://www.birmingham.ac.uk/staff/profiles/chemistry/simpkins-nigel.aspx
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"Nigel Simpkins"
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Publications

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Saint-Dizier F, Simpkins NS. (2017) First total synthesis of concavine. Chemical Science. 8: 3384-3389
Simpkins NS, Foster R, Lenz E, et al. (2017) Organocatalytic Stereoconvergent Synthesis of α-CF3 Amides; Triketopiperazines and Their Heterocyclic Metamorphosis. Chemistry (Weinheim An Der Bergstrasse, Germany)
Cabanillas A, Davies CD, Male L, et al. (2015) Highly enantioselective access to diketopiperazinescinchona alkaloid catalyzed Michael additions. Chemical Science. 6: 1350-1354
Hayes CJ, Simpkins NS. (2013) Bridgehead enolate or bridgehead organolithium? DFT calculations provide insights into a difficult bridgehead substitution reaction in the synthesis of the polycyclic polyprenylated acylphloroglucinol (PPAP) nemorosone. Organic & Biomolecular Chemistry. 11: 8458-62
Simpkins NS, Pavlakos I, Weller MD, et al. (2013) The cascade radical cyclisation approach to prenylated alkaloids: synthesis of stephacidin A and notoamide B. Organic & Biomolecular Chemistry. 11: 4957-70
Simpkins NS, Weske DF, Male L, et al. (2013) Synthesis of fumaramide derived [3]rotaxanes as potential precursors for molecular boxes. Chemical Communications (Cambridge, England). 49: 5010-2
Simpkins NS. (2013) Adventures in bridgehead substitution chemistry: synthesis of polycyclic polyprenylated acylphloroglucinols (PPAPs). Chemical Communications (Cambridge, England). 49: 1042-51
Simpkins N, Pavlakos I, Male L. (2012) Rapid access to polycyclic indolines related to the stephacidin alkaloids using a radical cascade. Chemical Communications (Cambridge, England). 48: 1958-60
Simpkins NS, Taylor JD, Weller MD, et al. (2010) Synthesis of nemorosone via a difficult bridgehead substitution reaction Synlett. 639-643
Blake AJ, Hume SC, Li W, et al. (2010) ChemInform Abstract: Enantioselective Synthesis of Phospholanes Using Chiral Lithium Amide Desymmetrization. Cheminform. 33: no-no
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