“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. Ed201453, 1168–1171. (doi: 10.1002/anie.201409283)

99 ga


“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, Synthesis201446, 2701–2710. (doi: 10.1055/s-0034-1379042)

98 ga


“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. Ed201453, 10204–10208. (doi: 10.1002/anie.201404527)

97 ga


“DABCO-bis(sulfur dioxide), DABSO, as an easy-to-handle source of SO2: Sulfonamide preparation”, Edward J. Emmett and Michael C. Willis, Org. Synth201491, 125-136. (doi: 10.15227/orgsyn.091.0125)

96 ga


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)

95 ga


“DABSO-based, three-component, one-pot sulfone synthesis”, Alex S. Deeming, Claire J. Russell, Alan J. Hennessy and Michael C. Willis, Org. Lett201416, 150-153. (doi: 10.1021/ol403122a)

94 ga