Research in the group ranges across the total synthesis of biologically active natural products and structural analogues to the discovery and development of new synthetic methods. Professor Paterson retired in October 2021 and is no longer accepting graduate students and postdocs.

Stereocontrolled Synthesis of Bioactive Natural Products and Structural Analogues

Representative targets include rare anticancer polyketides of both marine and terrestrial origin such as 1-4 below. For example, dictyostatin (1) shares the same microtubule-stabilising mechanism as the clinically important anticancer drug Taxol, while spirastrellolide A (2) is a potent inhibitor of protein phosphatase 2A. Likewise, chivosazole A (3) and reidispongiolide A (4) are novel actin-interacting macrolides isolated from myxobacteria and marine sponges respectively, which also represent challenging synthetic targets. In all these cases, the initial uncertainty over the stereochemistry, combined with their natural scarcity, has adversely affected their development. Efficient and flexible synthetic routes for the modular construction of these and other complex polyketide natural products are being pursued to establish their full configurations and provide a sustainable supply for detailed biological evaluation. A parallel objective is to design simplified analogues and hybrids that retain the exceptional cancer cell growth inhibitory properties whilst increasing their synthetic accessibility.

New Synthetic Methods

There is a need for new and more efficient methods of synthesis, particularly ones that achieve high levels of stereochemical control, where the development of asymmetric aldol methodology is of particular interest. These new methods are being applied to the synthesis of a wide variety of biologically important natural products.

Selected Publications

  • Dictyostatin and hybrids with discodermolide and taxol. Chem. Asian J. (2011), 6, 459; Tetrahedron (2010), 66, 6534
  • Spirastrellolide A. Angew. Chem. Int. Ed. (2012), 51, 2749; Org. Biomol. Chem.  (2012), 10, 5861 and 5873
  • Polyketide natural products as anticancer drug candidates. Org. Lett.  (2013), 15, 3118; Angew. Chem. Int. Ed. (2013), 52, 6517; Angew. Chem. Int. Ed. (2011), 50, 3219Curr. Opin. Drug Discov. Devel. (2010), 13, 777
  • Natural product synthesis using asymmetric aldol reactions. Angew. Chem. Int. Ed. (2013), 52, 9097

Publications

Synthesis of antimicrofilament marine macrolides: Synthesis and configurational assignment of a C5–C16 degradation fragment of reidispongiolide A
I Paterson, R Britton, K Ashton, H Knust, J Stafford
Proceedings of the National Academy of Sciences
(2004)
101
A quantitative evaluation of the effects of inhibitors of tubulin assembly on polymerization induced by discodermolide, epothilone B, and paclitaxel.
DA Dabydeen, GJ Florence, I Paterson, E Hamel
Cancer chemotherapy and pharmacology
(2004)
53
Stereochemical determination of dictyostatin, a novel microtubule-stabilising macrolide from the marine sponge Corallistidae sp.Electronic supplementary information (ESI) available: copies of 1D and 2D NMR spectra, tables of spectral data and calculated torsion angles. See http://www.rsc.org/suppdata/cc/b3/b316390c/
I Paterson, R Britton, O Delgado, AE Wright
Chemical communications (Cambridge, England)
(2004)
Synthesis of Novel 11-Desmethyl Analogues of Laulimalide by Nozaki−Kishi Coupling
I Paterson, H Bergmann, D Menche, A Berkessel
Organic letters
(2004)
6
Phorboxazole B synthetic studies: construction of C(1-32) and C(33-46) subtargets
I Paterson, A Steven, CA Luckhurst
Org Biomol Chem
(2004)
2
Total synthesis of spongistatin 1 (altohyrtin A): a tale of ten aldols
I Paterson, MJ Coster
(2004)
Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 5:  Linkage of Fragments C1-6 and C7-24 and Finale
SJ Mickel, D Niederer, R Daeffler, A Osmani, E Kuesters, E Schmid, K Schaer, R Gamboni, WC Chen, E Loeser, FR Kinder, K Konigsberger, K Prasad, TM Ramsey, J Repic, RM Wang, G Florence, I Lyothier, I Paterson
Organic Process Research & Development
(2003)
8
Large-scale synthesis of the anti-cancer marine natural product (+)-discodermolide. Part 4: Preparation of fragment C7-24
SJ Mickel, GH Sedelmeier, D Niederer, F Schuerch, M Seger, K Schreiner, R Daeffler, A Osmani, D Bixel, O Loiseleur, J Cercus, H Stettler, K Schaer, R Gamboni, A Bach, GP Chen, WC Chen, P Geng, GT Lee, E Loeser, J McKenna, FR Kinder, K Konigsberger, K Prasad, TM Ramsey, N Reel, O Repic, L Rogers, WC Shieh, RM Wang, L Waykole, S Xue, G Florence, I Paterson
Organic Process Research & Development
(2003)
8
Synthesis of novel discodermolide analogues with modified hydrogen-bonding donor/acceptor sites
I Paterson, O Delgado
Tetrahedron Letters
(2003)
44
Stereocontrolled Total Synthesis of (−)-Callipeltoside A
I Paterson, RDM Davies, AC Heimann, R Marquez, A Meyer
Organic letters
(2003)
5

Research Interest Group

Telephone number

01223 336407

Email address

College