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 elaiolide.
I Paterson, HG Lombart, C Allerton
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(1999)
218
Stereocontrolled synthesis of concanamycin F using chiral boron enolates.
I Paterson, VA Doughty, M McLeod
ABSTR PAP AM CHEM S
(1999)
218
Studies towards the synthesis of lophotoxin and pukalide: Synthesis of the 14-membered macrocyclic core and some acyclic structural analogues
I Paterson, RE Brown, CJ Urch
Tetrahedron Letters
(1999)
40
Total Synthesis of Elaiolide Using a Copper(I)-Promoted Stille Cyclodimerization Reaction
I Paterson, HG Lombart, C Allerton
Organic Letters
(1999)
1
Laboratory emulation of polyketide biosynthesis: an iterative, aldol-based, synthetic entry to polyketide libraries using (R)- and (S )-1-(benzyloxy)-2-methylpentan-3-one, and conformational aspects of extended polypropionates
I Paterson, JP Scott
Journal of the Chemical Society Perkin Transactions 1
(1999)
anti-Aldol reactions of lactate-derived ketones. Application to the synthesis of (−)-tetrahydrolipstatin
I Paterson, VA Doughty
Tetrahedron Letters
(1999)
40
Synthesis of cytotoxic marine macrolides: an aldol-based approach to spongistatin 1 (altohyrtin A)
I Paterson, KR Gibson, LE Keown, RD Norcross, RM Oballa
(1999)
Stereocontrolled synthesis of polyketide libraries: Boron-mediated aldol reactions with aldehydes on solid support
C Gennari, S Ceccarelli, U Piarulli, K Aboutayab, M Donghi, I Paterson
Tetrahedron
(1998)
54
Studies in marine macrolide synthesis: Synthesis of a fully functionalised C1C28 subunit of spongistatin 1 (altohyrtin A)
I Paterson, DJ Wallace, RM Oballa
Tetrahedron Letters
(1998)
39
Towards the total synthesis of phorboxazoles A and B: Stereocontrolled synthesis of a C20C32 subunit
I Paterson, EA Arnott
Tetrahedron Letters
(1998)
39

Research Interest Group

Telephone number

01223 336407

Email address

College