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

The total synthesis of scytophycin C. Part 2: synthesis of scytophycin C from the protected seco acid
I Paterson, C Watson, KS Yeung, RA Ward, PA Wallace
Tetrahedron
(1998)
54
The Total Synthesis of Scytophycin C. Part 1: Stereocontrolled Synthesis of the C1-C32 Protected Seco Acid
I Paterson, KS Yeung, C Watson, RA Ward, PA Wallace
Tetrahedron
(1998)
54
Studies in marine macrolide synthesis: Construction of a 24-membered macrocyclic intermediate for aplyronine A
I Paterson, MD Woodrow, CJ Cowden
Tetrahedron Letters
(1998)
39
Studies in marine macrolide synthesis: Stereocontrolled synthesis of the C1C11 and C15C27 subunits of aplyronine A
I Paterson, CJ Cowden, MD Woodrow
Tetrahedron Letters
(1998)
39
A facile oxidation/deprotection of electron rich silyl ethers using DDQ
I Paterson, CJ Cowden, VS Rahn, MD Woodrow
SYNLETT
(1998)
Polyketide synthesis using the boron-mediated, anti-aldol reactions of lactate-derived ketones: Total synthesis of (-)-ACRL, toxin IIIB
I Paterson, DJ Wallace, CJ Cowden
Synthesis
(1998)
1998
Epoxides in asymmetric synthesis. Enantioselective opening by nucleophiles promoted by chiral transition metal complexes.
I Paterson, DJ Berrisford
(1998)
Studies in marine macrolide synthesis: Synthesis of a C16-C28 subunit of spongistatin 1 (altohyrtin A) incorporating the CD-spiroacetal moiety.
I Paterson, DJ Wallace, KR Gibson
Tetrahedron Letters
(1997)
38
Studies in marine macrolide synthesis: Synthesis of the C-1-C-15 subunit of spongistatin 1 (altohyrtin A) and 15,16-anti aldol coupling reactions
I Paterson, RM Oballa
Tetrahedron Letters
(1997)
38
Polyketide library synthesis: Iterative assembly of extended polypropionates using (R)- and (S)-1-(benzyloxy)-2-methylpentan-3-one
I Paterson, JP Scott
Tetrahedron Letters
(1997)
38

Research Interest Group

Telephone number

01223 336407

Email address

College