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

Total synthesis of the esterase inhibitor (±)-ebelactone a using an aldol-claisen strategy
I PATERSON, AN HULME
Tetrahedron Letters
(1990)
31
Stereoselective aldol reactions of β-chlorovinyl ketones using dienol borinates: A new synthesis of dihydropyrones.
I PATERSON, S OSBORNE
Tetrahedron Letters
(1990)
31
Aldol reactions in polypropionate synthesis: High π-face selectivity of enol borinates from α-chiral methyl and ethyl ketones under substrate control
I Paterson, JM Goodman, M Isaka
Tetrahedron Letters
(1989)
30
Studies in marine cembranolide synthesis: A synthesis of 2,3,5-trisubstituted furan intermediates for lophotoxin and pukalide
I PATERSON, M GARDNER, BJ BANKS
Tetrahedron
(1989)
45
Studies in polyether synthesis: Controlled bisepoxide cyclisation using a β-diketone group
I PATERSON, PA CRAW
Tetrahedron Letters
(1989)
30
A short asymmetric synthesis of a C19–C27 segment of rifamycin S. Kinetic resolution in the aldol reactions of ethylketones using chiral boron reagents
I PATERSON, CK MCCLURE, RC SCHUMANN
Tetrahedron Letters
(1989)
30
Studies in macrolide synthesis: A highly stereoselective synthesis of (+)-(9S)-dihydroerythronolide a using macrocyclic stereocontrol
I PATERSON, DJ RAWSON
Tetrahedron Letters
(1989)
30
Aldol reactions of methylketones using chiral boron reagents: A reversal in aldehyde enantioface selectivity
I Paterson, JM Goodman
Tetrahedron Letters
(1989)
30
THEORETICAL-STUDIES OF ALDOL STEREOSELECTIVITY - THE DEVELOPMENT OF A FORCE-FIELD MODEL FOR ENOL BORINATES AND THE INVESTIGATION OF CHIRAL ENOLATE PI-FACE SELECTIVITY
J GOODMAN, I PATERSON, S KAHN
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(1988)
196
NEW ASYMMETRIC ALDOL METHODOLOGY USING BORON ENOLATES
I PATERSON
CHEMISTRY & INDUSTRY
(1988)

Research Interest Group

Telephone number

01223 336407

Email address

College