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

Studies towards the total synthesis of Leiodermatolide
KK-H Ng, S Williams, I Paterson
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2013)
245
Studies toward the total synthesis of madeirolide A
GW Haslett, CI MacGregor, SP Fearnley, I Paterson
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2013)
245
Total synthesis of alotaketal A
M Xuan, I Paterson, S Dalby
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2013)
245
Synthesis of the C1-C11 western fragment of madeirolide A.
I Paterson, GW Haslett
Organic letters
(2013)
15
Total Synthesis of Alotaketal A
M Xuan, I Paterson, SM Dalby
Org Lett
(2012)
14
The stereocontrolled total synthesis of spirastrellolide A methyl ester. Fragment coupling studies and completion of the synthesis.
I Paterson, EA Anderson, SM Dalby, JH Lim, P Maltas
Organic & biomolecular chemistry
(2012)
10
The stereocontrolled total synthesis of spirastrellolide A methyl ester. Expedient construction of the key fragments.
I Paterson, EA Anderson, SM Dalby, JH Lim, P Maltas, O Loiseleur, J Genovino, C Moessner
Organic & Biomolecular Chemistry
(2012)
10
A Second-Generation Total Synthesis of Spirastrellolide A Methyl Ester
I Paterson, P Maltas, SM Dalby, JH Lim, EA Anderson
Angew Chem Int Ed Engl
(2012)
51
Stereocontrolled total synthesis of (+)-concanamycin F: the strategic use of boron-mediated aldol reactions of chiral ketones
I Paterson, VASN Doughty, MD McLeod, T Trieselmann
Tetrahedron
(2011)
67
Synthesis of the Macrocyclic Core of Leiodermatolide
I Paterson, T Paquet, SM Dalby
Org Lett
(2011)
13

Research Interest Group

Telephone number

01223 336407

Email address

College