Department of Chemistry

portrait of Dr Finian Leeper

Dr Finian Leeper

Emmanuel College

Groups: Leeper group website

Telephone: 01223 336403

E-mail: fjl1@cam.ac.uk

 

 


General


Coenzyme Chemistry. Thiamin diphosphate (TPP) 1 is a coenzyme used by many enzymes which make and break bonds adjacent to keto groups. We have synthesised deaza analogues (e.g. 2) of intermediates in these reactions. These bind extremely tightly to TPP-dependent enzymes. We aim to make further analogues that are inhibitors of specific enzymes and may thus be of medicinal importance. We also hope to get crystal structures of the analogues bound to their target enzymes which should help to understand how the reactions occur.

Novel Catalysts. Thiazolium salts catalyse a variety of reactions involving making and breaking bonds to a carbonyl carbon (e.g. the benzoin condensation). We have made chiral thiazolium salts (e.g. 3) and have observed asymmetric induction in formation of benzoin. We intend to further develop these catalysts to obtain better levels of asymmetric induction, to probe the mechanism and to introduce binding cavities for increased rate and better selectivities.

Enzyme Chemistry. A key step in tetrapyrrole biosynthesis is the linking of four molecules of the monopyrrole PBG (4) to give a linear tetrapyrrole, catalysed by PBG deaminase. A crystal structure is available and we plan to use this to design and then synthesise analogues of PBG which bind tightly to the enzyme. These will aid understanding of the mechanism and may be of value as antibiotics and/or herbicides.

Biosynthesis of Prodigiosin. (with Prof G. Salmond, Biochemistry) Prodigiosin (see below) is an immunosuppressant with a novel mode of action. We have found the cluster of genes that codes for its biosynthesis in Serratia marcescens and are working on the elucidation of the biosynthetic pathway and the mechanisms of the enzymic reactions involved.

Synthetic Methods for PET. (with Dr F. Aigbirhio, Wolfson Brain Imaging Centre) Positron Emission Tomography (PET) is a technique used for scanning human brain to detect the distribution of compounds of diagnostic interest. It relies on compounds labelled with very short- lived radioisotopes (e.g. 11C or 18F). The whole synthesis of such compounds must not take longer than ~30 mins. The aim of this project is to develop new synthetic methods, using polymer-supported reagents, that will allow such rapid synthesis and isolation of labelled compounds of neuropharmacological importance.

Selected Publications

Prodigiosin Biosynthesis: Molec.Microbiol. (2005), 56, 971-89. Chem. Commun. (2008), 1862–1864

Coenzyme Chemistry: FEBS J. (2009), 276, 2905–2916. Org. Biomolec. Chem. (2008), 6, 3561-3572.

Enzyme Chemistry: Org. Biomolec. Chem. (2003), 1, 21-23 and 1443-1446.

Thiazolium Salts: J. Org. Chem. (2001) 66, 5124-5131, J. Chem. Soc., Perkin Trans.1 (1998), 1891.

Research Interests


 

Teaching


Personal


Publications

Publications

Synthesis of and asymmetric induction by chiral polycyclic thiazolium salts
AU Gerhard, FJ Leeper - TETRAHEDRON LETT (1997) 38, 3615
(DOI: 10.1016/S0040-4039(97)00682-5)
Synthesis of and asymmetric induction by chiral bicyclic thiazolium salts
RL Knight, FJ Leeper - TETRAHEDRON LETT (1997) 38, 3611
(DOI: 10.1016/S0040-4039(97)00681-3)
Synthetic studies relevant to biosynthetic research on vitamin B-12 .12. Modification of the periphery of chlorins and isobacteriochlorins
JJ DeVoss, FJ Leeper, AR Battersby - J CHEM SOC PERK T 1 (1997), 1105
(DOI: 10.1039/a607852d)
Synthesis of tetrahydroquinolines, hexahydrobenzoindolizines and an aryl phosphonate linker for the generation of catalytic antibodies
C GonzalezBello, C Abell, FJ Leeper - J CHEM SOC PERK T 1 (1997), 1017
(DOI: 10.1039/a606968a)
Synthesis of analogues of porphobilinogen
FJ Leeper, M Rock, D Appleton - J CHEM SOC PERK T 1 (1996), 2633
(DOI: 10.1039/p19960002633)
Interaction of analogues of porphobilinogen with porphobilinogen deaminase
FJ Leeper, M Rock - J CHEM SOC PERK T 1 (1996), 2643
(DOI: 10.1039/p19960002643)
Biosynthesis of porphyrins and related macrocycles .45. Determination by a novel X-ray method of the absolute configuration of the spiro lactam which inhibits uroporphyrinogen III synthase (cosynthetase)
AC Spivey, A Capretta, CS Frampton, FJ Leeper, AR Battersby - J CHEM SOC PERK T 1 (1996), 2091
(DOI: 10.1039/p19960002091)
Biosynthesis of porphyrins and related macrocycles .44. Synthetic and stereochemical studies on the proposed spiro intermediate for biosynthesis of the natural porphyrins
MA Cassidy, N Crockett, FJ Leeper, AR Battersby - J CHEM SOC PERK T 1 (1996), 2079
(DOI: 10.1039/p19960002079)
Deuterium isotope effects on porphobilinogen synthesis catalysed by 5-aminolaevulinic acid dehydratase
D Appleton, FJ Leeper - Bioorganic and Medicinal Chemistry Letters (1996) 6, 1191
(DOI: 10.1016/0960-894X(96)00199-0)
Mechanism-based inhibition of 5-aminolaevulinic acid dehydratase from Bacillus subtilis by the 3-thia analogue of the substrate
D Appleton, FJ Leeper - Chemical Communications (1996), 303
(DOI: 10.1039/cc9960000303)

 


 

Funding