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

Synergistic interactions between peloruside A and other microtubule-stabilizing and destabilizing agents in cultured human ovarian carcinoma cells and murine T cells
A Wilmes, D O'Sullivan, A Chan, C Chandrahasen, I Paterson, PT Northcote, ACL Flamme, JH Miller
Cancer Chemotherapy and Pharmacology
(2011)
68
Insights into the interaction of Discodermolide and Docetaxel with Tubulin. Mapping the Binding Sites of Microtubule-Stabilizing Agents by Using an Integrated NMR and Computational Approach
A Canales, J Rodríguez-Salarichs, C Trigili, L Nieto, C Coderch, JM Andreu, I Paterson, J Jiménez-Barbero, JF Díaz
ACS Chemical Biology
(2011)
6
Structure-activity studies of the pelorusides: new congeners and semi-synthetic analogues.
AJ Singh, M Razzak, P Teesdale-Spittle, TN Gaitanos, A Wilmes, I Paterson, JM Goodman, JH Miller, PT Northcote
Organic & biomolecular chemistry
(2011)
9
Strategy evolution in the total synthesis of SpirastrellolideA methyl ester
I Paterson, SM Dalby, P Maltas
Israel Journal of Chemistry
(2011)
51
Leiodermatolide, a potent antimitotic macrolide from the marine sponge Leiodermatium sp.
I Paterson, SM Dalby, JC Roberts, GJ Naylor, EA Guzmán, R Isbrucker, TP Pitts, P Linley, D Divlianska, JK Reed, AE Wright
Angew Chem Int Ed Engl
(2011)
50
Total synthesis and biological evaluation of a series of macrocyclic hybrids and analogues of the antimitotic natural products dictyostatin, discodermolide, and taxol.
I Paterson, GJ Naylor, NM Gardner, E Guzmán, AE Wright
Chem Asian J
(2011)
6
Synthesis of polyketide natural products and analogs as promising anticancer agents.
SM Dalby, I Paterson
Curr Opin Drug Discov Devel
(2010)
13
Synthesis of the C15-C35 Northern Hemisphere Subunit of the Chivosazoles
I Paterson, LJ Gibson, SBJ Kan
Org Lett
(2010)
12
Synthetic studies towards the aplyronines: Potent anticancer marine macrolides isolated from Aplysia kurodai
SJ Fink, LYW Lee, I Paterson
ABSTR PAP AM CHEM S
(2010)
240
Total synthesis of novel analogs of dictyostatin
EG Williams, I Paterson
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2010)
240

Research Interest Group

Telephone number

01223 336407

Email address

College