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 Swinholide A and Hemiswinholide A
I PATERSON, KS YEUNG, RA WARD, JG CUMMING, JD SMITH
Journal of the American Chemical Society
(2002)
116
STUDIES IN MACROLIDE SYNTHESIS - A STEREOCONTROLLED SYNTHESIS OF OLEANDOLIDE EMPLOYING REAGENT-CONTROLLED AND SUBSTRATE-CONTROLLED ALDOL REACTIONS OF (S)-1-(BENZYLOXY)-2-METHYLPENTAN-3-ONE
I PATERSON, RD NORCROSS, RA WARD, P ROMEA, MA LISTER
Journal of the American Chemical Society
(2002)
116
Stereoselective synthesis of the chiral sequence of erythronolide A
G STORK, I PATERSON, FKC LEE
Journal of the American Chemical Society
(2002)
104
STEREOCONTROLLED SYNTHESIS OF A C1-C15 SEGMENT FOR THE MARINE MACROLIDES SWINHOLIDE-A AND SCYTOPHYCIN-C - USE OF A VINYLOGOUS MUKAIYAMA ALDOL REACTION
I PATERSON, JD SMITH
The Journal of Organic Chemistry
(2002)
57
HIGH PI-FACE SELECTIVITY IN ANTI-ALDOL REACTIONS OF E-ENOL BORINATES FROM CHIRAL ALKOXYMETHYL KETONES - STEREOCONTROLLED SYNTHESIS OF A C24-C32 POLYOL SUBUNIT OF RAPAMYCIN
I PATERSON, RD TILLYER
The Journal of Organic Chemistry
(2002)
58
Total Synthesis of (-)-Ebelactone A and B
I PATERSON, AN HULME
The Journal of Organic Chemistry
(2002)
60
Theoretical Studies of Aldol Stereoselectivity: The Development of a Force Field Model for Enol Borinates and the Investigation of Chiral Enolate π-Face Selectivity
JM Goodman, SD Kahn, I Paterson
The Journal of Organic Chemistry
(2002)
55
Total synthesis of altohyrtin A (spongistatin 1): an alternative synthesis of the CD-spiroacetal subunit
I Paterson, MJ Coster
Tetrahedron Letters
(2002)
43
Total Synthesis of Siphonarin B and Dihydrosiphonarin B
I Paterson, DY-K Chen, AS Franklin
Org Lett
(2002)
4
Boron-mediated aldol reactions of ethyl alpha-(N,N)-dibenzylamino ketones: control of enolisation geometry and aldehyde pi-facial selectivity
I Paterson, AC Mackay
Tetrahedron Letters
(2001)
42

Research Interest Group

Telephone number

01223 336407

Email address

College