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

Computer-assisted design of chiral boron enolates: The role of ate complexes in determining aldol stereoselectivity.
A Bernardi, A Comotti, C Gennari, CT Hewkin, JM Goodman, A Schlapbach, I Paterson
Tetrahedron
(1994)
50
Studies in marine macrolide synthesis: Boron and silicon-mediated coupling strategies for Swinholide A
I PATERSON, JG CUMMING, JD SMITH, RA WARD
Tetrahedron Letters
(1994)
35
Recent developments in asymmetric aldol methodology
I Paterson, AS Franklin
Contemporary Organic Synthesis
(1994)
1
Studies in biomimetic polyether synthesis: Construction of an ABCD-ring subunit of etheromycin using polyepoxide cascade cyclisations.
I PATERSON, RD TILLYER, JB SMAILL
Tetrahedron Letters
(1993)
34
Studies in marine macrolide synthesis: Asymmetric synthesis of C1-C15/C16 subunits of swinholide A and scytophycin C.
I PATERSON, JD SMITH
Tetrahedron Letters
(1993)
34
Studies in marine macrolide synthesis: A stereocontrolled synthesis of a C17-C32 subunit of scytophycin C.
I PATERSON, KS YEUNG
Tetrahedron Letters
(1993)
34
1,3-ASYMMETRIC INDUCTION IN THE ALDOL REACTIONS OF ALPHA-METHYLENE-BETA-ALKOXY ALDEHYDES
I PATERSON, S BOWER, RD TILLYER
Tetrahedron Letters
(1993)
34
Studies in biomimetic polyether synthesis: Synthesis of an A-ring subunit of etheromycin
I PATERSON, RD TILLYER, GR RYAN
Tetrahedron Letters
(1993)
34
Origins of stereoselectivity in the addition of chiral allyl- and crotylboranes to aldehydes: the development and application of a force field model of the transition state
A Vulpetti, M Gardner, C Gennari, A Bernardi, JM Goodman, I Paterson
The Journal of Organic Chemistry
(1993)
58
Origins of π-face selectivity in the aldol reactions of chiral E-enol borinates: a computational study using transition state modelling.
A Vulpetti, A Bernardi, C Gennari, JM Goodman, I Paterson
Tetrahedron
(1993)
49

Research Interest Group

Telephone number

01223 336407

Email address

College