Details of Grant 

EPSRC Reference:	EP/E041302/1
Title:	New Tandem Approaches to Functionalised Cyclopropanes: Development and Applications
Principal Investigator:	Taylor, Professor R
Other Investigators:
Researcher Co-Investigators:
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Department:	Chemistry
Organisation:	University of York
Scheme:	Standard Research
Starts:	01 October 2007	Ends:	30 September 2010	Value (£):	107,950
EPSRC Research Topic Classifications:	Chemical Synthetic Methodology
EPSRC Industrial Sector Classifications:	Chemicals Pharmaceuticals and Biotechnology
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Panel History:
Summary on Grant Application Form
We have recently developed a range of manganese dioxide-mediated tandem oxidation processes (TOPs) in which primary alcohols are oxidised and the intermediate aldehydes are trapped in situ to give alkenes, alkynes, imines, oximes, amines, nitriles, esters, amides and heterocyclic systems via one-pot procedures. These TOP sequences offer a number of advantages to the synthetic organic chemist, both in academic/medical research and in scale-up applications: they are operationally straightforward, the MnO2 and its by-products being removed by a simple filtration; they result in a reduced number of operations, giving significant time-cost benefits; they allow the use of difficult carbonyl intermediates (i.e. those that are volatile, toxic or noxious) as they are prepared and elaborated in situ. These initial studies concentrated on 1,2-additions to the intermediate carbonyl compounds, such as oxidation-Wittig and oxidation-imination sequences.The main aim of this proposal is to extend the above methodology to allylic alcohols so that the intermediate aldehydes are trapped by sulfuranes in a 1,4-manner to produce cyclopropane aldehydes (potentially in an asymmetric process), which can themselves be further elaborated in situ. This would lead to novel one-pot, multi-step processes to prepare highly functionalised cyclopropanes suitable for elaboration into carbocyclic and heterocyclic building blocks, natural products and biologically active analogues. The adventurous element concerns the telescoping of a number of seemingly incompatible processes (e.g. oxidation, cyclopropanation, Wittig olefination, ring exansion) into a single operation, with consequent practical, economic and environmental benefits. The application of this methodology in target synthesis will also be explored. Possible targets include the insecticidal pyrethroid analogues allethrin and allethrin II, secolepidozane (cytotoxic) and dysibetaine CPb (glutamate agonist).
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Organisation Website:	http://www.york.ac.uk