2014

“Combining organometallic reagents, the sulfur dioxide surrogate DABSO and amines: A one-pot preparation of sulfonamides, amenable to array synthesis”, Alex S. Deeming, Claire J.  Russell and Michael C. Willis, Angew. Chemie. Int. Ed. 2014, 53, 1168–1171. (doi: 10.1002/anie.201409283)

“Rediscovering the chemistry of sulfur dioxide: New developments in synthesis and catalysis”, Alex S. Deeming, Edward J. Emmett, Charlotte S. Richards-Taylor and Michael C. Willis, Synthesis, 2014, 46, 2701–2710. (doi: 10.1055/s-0034-1379042)

“Palladium-catalyzed synthesis of ammonium sulfinates from aryl halides and the sulfur dioxide-Surrogate DABSO: A gas and reductant free process”, Edward J. Emmett, Barry R. Hayter and Michael C. Willis, Angew. Chemie. Int. Ed. 2014, 53, 10204–10208. (doi: 10.1002/anie.201404527)

“DABCO-bis(sulfur dioxide), DABSO, as an easy-to-handle source of SO₂: Sulfonamide preparation”, Edward J. Emmett and Michael C. Willis, Org. Synth. 2014, 91, 125-136. (doi: 10.15227/orgsyn.091.0125)

Michael C. Willis, Hydroacylation of alkenes, alkynes and allenes. In: Gary A. Molander and Paul Knochel (eds.), Comprehensive Organic Synthesis, 2nd Edition, Vol 4, Oxford: Elsevier; 2014, pp. 961- 994. (doi: 10.1016/B978-0-08-097742-3.00423-7)

“DABSO-based, three-component, one-pot sulfone synthesis”, Alex S. Deeming, Claire J. Russell, Alan J. Hennessy and Michael C. Willis, Org. Lett. 2014, 16, 150-153. (doi: 10.1021/ol403122a)