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

Remote, 1,5-anti stereoinduction in the boron-mediated aldol reactions of beta-oxygenated methyl ketones.
I Paterson, KR Gibson, RM Oballa
Tetrahedron Letters
(1996)
37
Anti aldol reactions of alpha-alkoxymethyl ketones: Application to the total synthesis of (+)-restricticin.
I Paterson, T Nowak
Tetrahedron Letters
(1996)
37
Two Complimentary Methods for the Synthesis of the Terminal N-Alkenyl-N-methylformamide Group Found in Cytotoxic Marine Macrolides
I Paterson, C Cowden, C Watson
Synlett
(1996)
1996
Total synthesis of (-)-denticulatins A and B using efficient methods of acyclic stereocontrol.
I Paterson, MV Perkins
Tetrahedron
(1996)
52
A computational model for stereoselectivity in the boron-mediated aldol reactions of methyl ketones
I Paterson, A Bernardi, C Gennari, JM Goodman
(1996)
Studies in macrolide synthesis: A sequential aldol/glycosylation approach to the synthesis of concanamycin A
I PATERSON, MD MCLEOD
Tetrahedron Letters
(1995)
36
THE TOTAL SYNTHESIS OF SWINHOLIDE-A .3. A STEREOCONTROLLED SYNTHESIS OF (-)-PRE-SWINHOLIDE-A
I PATERSON, RA WARD, JD SMITH, JG CUMMING, KS YEUNG
Tetrahedron
(1995)
51
THE TOTAL SYNTHESIS OF SWINHOLIDE-A .4. SYNTHESIS OF SWINHOLIDE-A AND ISOSWINHOLIDE-A FROM THE PROTECTED MONOMERIC SECO ACID, PRE-SWINHOLIDE-A
I PATERSON, KS YEUNG, RA WARD, JD SMITH, JG CUMMING, S LAMBOLEY
Tetrahedron
(1995)
51
The total synthesis of swinholide A. Part 2: A stereocontrolled synthesis of a c1–c15 segment
I PATERSON, JD SMITH, RA WARD
Tetrahedron
(1995)
51
The total synthesis of swinholide A. Part 1: A stereocontrolled synthesis of a C19-C32 segment
I PATERSON, JG CUMMING, RA WARD, S LAMBOLEY
Tetrahedron
(1995)
51

Research Interest Group

Telephone number

01223 336407

Email address

College