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Professor Chris Willis
Professor Chris Willis
B.Sc.(Lond.), D.Phil.(Sus.)
Professor of Organic Chemistry
Area of research
Natural Products: Synthesis and Biosynthesis
Summary
Natural products isolated from bacteria, fungi and plants from both marine and terrestrial environments are a rich source of compounds of medicinal and agrochemical importance. We have published >130 papers which centre upon:-
- Structure elucidation and total synthesis of natural products
- Design and synthesis of probes to elucidate biosynthetic pathways and enzyme mechanisms
- Enantioselective synthesis of amino acids and heterocycles
- Isotopic labelling, biotransformations and reaction mechanisms
Professor Willis is a supervisor in the EPSRC Centre for Doctoral Training in Chemical Synthesis
Keywords
- natural products
- bacteria
- fungi
- plants
- compounds
- biosynthetic pathways
- enzyme mechanisms
- amino acids
Expertise
Natural products isolated from bacteria, fungi and plants from both marine and terrestrial environments are a rich source of compounds of medicinal and agrochemical importance. We have published >100 papers which centre upon:-
? Structure elucidation and total synthesis of natural products
? Design and synthesis of probes to elucidate biosynthetic pathways and enzyme mechanisms
? Enantioselective synthesis of amino acids and heterocycles
? Isotopic labelling, biotransformations and reaction mechanisms
natural productsbacteriafungiplantscompoundsbiosynthetic pathwaysenzyme mechanisms
Recent publications
- Connolly, JA, Wilson, A, Macioszek, M, Song, Z, Wang, L, Mohammad, HH, Yadav, M, Martino, Md, Miller, CE, Hothersall, J, Haines, AS, Stephens, ER, Crump, MP, Willis, CL, Simpson, TJ, Winn, PJ & Thomas, CM, 2019, Defining the genes for the final steps in biosynthesis of the complex polyketide antibiotic mupirocin by Pseudomonas fluorescens NCIMB10586. Scientific Reports, vol 9.
- Donnelly, B, Elliott, L, Willis, C & Booker-Milburn, K, 2019, Sequential Photochemical and Prins Reactions for the Diastereoselective Synthesis of Tricyclic Scaffolds. Angewandte Chemie - International Edition.
- Lees, NR, Han, L-C, Byrne, M, Davies, J, Parnell, A, Moreland, P, Stach, JEM, Kamp, MVd, Willis, C & Race, P, 2019, An Esterase-like Lyase Catalyzes Acetate Elimination in Spirotetronate/Spirotetramate Biosynthesis. Angewandte Chemie - International Edition, vol 58., pp. 2305-2309
- Szwalbe, AJ, Williams, K, Song, Z, De Mattos-Shipley, K, Vincent, JL, Bailey, AM, Willis, CL, Cox, RJ & Simpson, TJ, 2019, Characterisation of the biosynthetic pathway to agnestins A and B reveals the reductive route to chrysophanol in fungi. Chemical Science, vol 10., pp. 233-238
- Marsh, CO, Lees, NR, Han, L-C, Byrne, MJ, Mbatha, SZ, Maschio, L, Pagden-Ratcliffe, S, Duke, P, Stach, JEM, Curnow, P, Willis, CL & Race, PR, 2019, A Natural Diels-Alder Biocatalyst Enables Efficient [4 + 2] Cycloaddition Under Harsh Reaction Conditions. ChemCatChem.
- Walker, P, Williams, C, Weir, A, Wang, L, Crosby, J, Race, P, Simpson, T, Willis, C & Crump, M, 2019, Control of beta-Branching in Kalimantacin Biosynthesis: Application of Direct Observe 13C NMR to Polyketide Programming.. Angewandte Chemie, vol 58., pp. 12446-12450
- Greco, C, Mattos-Shipley, Kd, Bailey, AM, Mulholland, NP, Vincent, JL, Willis, CL, Cox, RJ & Simpson, TJ, 2019, Structure revision of cryptosporioptides and determination of the genetic basis for dimeric xanthone biosynthesis in fungi. Chemical Science, vol 10., pp. 2930-2939
- Nofiani, R, Mattos-Shipley, Kd, Lebe, KE, Han, LC, Iqbal, Z, Bailey, AM, Willis, CL, Simpson, TJ & Cox, RJ, 2018, Strobilurin biosynthesis in Basidiomycete fungi. Nature Communications, vol 9.
- Hayashi, R, Shimizu, A, Davies, J, Ishizaki, Y, Willis, C & Yoshida, 2018, Metal‐ and Oxidant‐Free Alkenyl C−H/Aromatic C−H Cross‐Coupling Using Electrochemically Generated Iodosulfonium Ions. Angewandte Chemie - International Edition, vol 57., pp. 12891-12895
- Maschio, L, Parnell, A, Lees, NR, Willis, C, Berger-Schaffitzel, C, Stach, JEM & Race, P, 2018, Cloning, Expression and Purification of Intact Polyketide Synthase Modules. in: [forthcoming Methods in Enzymology volume]. Elsevier Inc., pp. 63-82
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