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

O-Silylated dienolates in organic synthesis: γ-Selective alkylation of unsaturated carbonyl compounds by 1,5-dithienium fluoroborate.
I PATERSON, LG PRICE
Tetrahedron Letters
(1981)
22
ALPHA-ALKYLATION AND ALPHA-ALKYLIDENATION OF CARBONYL COMPOUNDS - LEWIS ACID-PROMOTED PHENYLTHIOALKYLATION OF O-SILYLATED ENOLATES
I PATERSON, I FLEMING
TETRAHEDRON LETTERS
(1979)
ALLYLSILANES IN ORGANIC-SYNTHESIS - METHOD FOR THE INTRODUCTION OF 2 CARBON SUBSTITUENTS IN PLACE OF CARBONYL OXYGEN
I Fleming*, I Paterson
Synthesis
(1979)
1979
GAMMA-ALKYLATION OF UNSATURATED-KETONES AND ESTERS - ZINC BROMIDE-CATALYSED ALKYLATION OF ORTHO-SILYLATED DIENOLATES
I FLEMING, J GOLDHILL, I PATERSON
TETRAHEDRON LETTERS
(1979)
GAMMA-SULFENYLATION OF ALPHA-BETA-UNSATURATED ALDEHYDES, KETONES, AND ESTERS - USE OF O-SILYLATED DIENOLATES
I FLEMING, J GOLDHILL, I PATERSON
TETRAHEDRON LETT
(1979)
ALPHA-ALKYLATION OF KETONES, ESTERS, AND LACTONES - ZINC BROMIDE-CATALYSED ALKYLATION OF O-SILYLATED ENOLATES, A SYNTHESIS OF (+/-)-AR-TURMERONE
I PATERSON
TETRAHEDRON LETTERS
(1979)
A Simple Synthesis of Carvone Using Silyl Enol Ethers
I Fleming*, I Paterson
Synthesis
(1979)
1979
ALPHA-METHYLENATION OF LACTONES AND ESTERS ZINC BROMIDE-CATALYZED PHENYLTHIOMETHYLATION OF OMICRON-SILYLATED ENOLATES
I PATERSON, I FLEMING
TETRAHEDRON LETT
(1979)
Regiospecific α-methylenation and α-methylation of ketones: titanium tetrachloride promoted phenylthiomethylation of silyl enol ethers
I Peterson, I Fleming
Tetrahedron Letters
(1979)
20
Free radical addition to olefins. Part 23. Kinetics of the addition of chloroiodomethane to ethylene and vinyl fluoride
I PATERSON, JM TEDDER, JC WALTON
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2
(1978)

Research Interest Group

Telephone number

01223 336407

Email address

College