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 (−)-Spirangien A, an Antimitotic Polyketide Isolated from the MyxobacteriumSorangium Cellulosum
I Paterson, AD Findlay, C Noti
Chemistry - An Asian Journal
(2009)
4
Total synthesis and biological evaluation of novel C2-C6 region analogues of dictyostatin
I Paterson, NM Gardner, E Guzmán, AE Wright
Bioorganic & Medicinal Chemistry
(2009)
17
Toward the total synthesis of the brasilinolides: Construction of a differentially protected C20-C38 segment
I Paterson, PM Burton, CJ Cordier, MP Housden, FA Mühlthau, O Loiseleur
Organic Letters
(2009)
11
Total synthesis of cytotoxic marine macrolides: Callipeltoside A, aurisides A and B, and dolastatin 19
I Paterson, AD Findlay
Pure and Applied Chemistry
(2009)
80
Total synthesis of novel dictyostatin analogs and hybrids as microtubule-stabilizing anticancer agents
I Paterson, NM Gardner, GJ Naylor
Pure and Applied Chemistry
(2009)
81
Synthesis and stereochemical determination of the spirastrellolides.
I Paterson, SM Dalby
Nat Prod Rep
(2009)
26
Progress toward a total synthesis of spirastrellolide A
I Paterson, EA Anderson, SM Dalby, JH Lim, O Loiseleur, P Maltas, C Moessner
Pure and Applied Chemistry
(2009)
79
Total synthesis of (−)-spirangien A and its methyl ester
I Paterson, AD Findlay, C Noti
Chem Commun (Camb)
(2008)
Toward the total synthesis of the brasilinolides: stereocontrolled assembly of a C1-C19 polyol segment.
I Paterson, FA Mühlthau, CJ Cordier, MP Housden, PM Burton, O Loiseleur
Organic letters
(2008)
11
Total synthesis and biological evaluation of potent analogues of dictyostatin: Modification of the C2-C6 dienoate region
I Paterson, NM Gardner, E Guzmán, AE Wright
Bioorganic & medicinal chemistry letters
(2008)
18

Research Interest Group

Telephone number

01223 336407

Email address

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