Department of Chemistry

portrait of Professor Steve Ley FRS

Professor Steve Ley FRS

Trinity College

Groups: Ley group website

Telephone: 01223 336442 (fax)
             01223 336398

E-mail: svl1000@cam.ac.uk


General


In the Ley Group, we specialise in developing new synthesis methods and applying them to the construction of biologically important molecules. Over the last 4 years we have completed the total synthesis of 38 natural products including spongistatin 1 (anti-mitotic agent), rapamycin (immunosuppressant), thapsigargin (SERCA pumps inhibitor), azadirachtin (insect antifeedant) and bengazole A (fungicide), taking our group total to 140 completed total syntheses. In addition to our research on natural product synthesis, we have the Innovative Technology Centre (ITC); a new state-of-the-art flow chemistry facility. Our group is also part of the CRUK PhD Training Programme in Medicinal Chemistry.

For more detailed research information, group members and our publication list please see the group website

Publications

A microcapillary flow disc reactor for organic synthesis
CH Hornung, MR Mackley, IR Baxendale, SV Ley - Organic Process Research and Development (2007) 11, 399
(DOI: 10.1021/op700015f)
Identification of a putative azadirachtin-binding complex from Drosophila Kc167 cells
SL Robertson, WT Ni, TS Dhadialla, AJ Nisbet, C McCusker, SV Ley, W Mordue, AJ Mordue - Archives of Insect Biochemistry and Physiology (2007) 64, 200
(DOI: 10.1002/arch.20171)
Optimisation of conditions for O-benzyl and N-benzyloxycarbonyl protecting group removal using an automated flow hydrogenator
KR Knudsen, J Holden, SV Ley, M Ladlow - Advanced Synthesis and Catalysis (2007) 349, 535
(DOI: 10.1002/adsc.200600558)
Total synthesis of thapsigargin, a potent SERCA pump inhibitor
M Ball, SP Andrews, F Wierschem, E Cleator, MD Smith, SV Ley - Organic Letters (2007) 9, 663
(DOI: 10.1021/ol062947x)
Total synthesis of rapamycin
ML Maddess, MN Tackett, H Watanabe, PE Brennan, CD Spilling, JS Scott, DP Osborn, SV Ley - Angew Chem Int Ed Engl (2007) 46, 591
(DOI: 10.1002/anie.200604053)
Total synthesis of rapamycin
ML Maddess, MN Tackett, H Watanabe, PE Brennan, CD Spilling, JS Scott, DP Osborn, SV Ley - Angewandte Chemie - International Edition (2007) 46, 591
Total synthesis of potent antifungal marine bisoxazole natural products bengazoles A and B
JA Bull, EP Balskus, RAJ Horan, M Langner, SV Ley - Chemistry (2007) 13, 5515
(DOI: 10.1002/chem.200700033)
Total synthesis of five thapsigargins: Guaianolide natural products exhibiting sub-nanomolar SERCA inhibition
SP Andrews, M Ball, F Wierschem, E Cleator, S Oliver, K Hogenauer, O Simic, A Antonello, U Hunger, MD Smith, SV Ley - Chemistry (2007) 13, 5688
(DOI: 10.1002/chem.200700302)
Synthesis of azadirachtin: a long but successful journey.
GE Veitch, E Beckmann, BJ Burke, A Boyer, SL Maslen, SV Ley - Angew Chem Int Ed Engl (2007) 46, 7629
(DOI: 10.1002/anie.200703027)
Solid supported reagents in multi-step flow synthesis.
IR Baxendale, SV Ley - Ernst Schering Foundation symposium proceedings (2007) 3, 151

 

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