Enantioselective cyclopropanation of enals by oxidative N-heterocyclic carbene catalysis

Anup Biswas, Suman De Sarkar, L. Tebben, Armido Studer

Chemical Communications · 2012 · 104 citations · 30 references

Concepts

Abstract

Carbene catalysed redox activation of α,β-unsaturated aldehydes is applied for generation of α,β-unsaturated acyl azoliums which undergo cyclopropanation upon reaction with a sulfur ylide and an alcohol to give the corresponding cyclopropanecarboxylic acid esters. With chiral carbenes good to excellent diastereo and enantioselectivities are obtained.

References

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