“Arylsulfonyl fluoride boronic acids: Preparation and coupling reactivity”, Terry Shing-Bong Lou, and Michael C. Willis, Tetrahedron 201975. (doi: 10.1016/j.tet.2019.130782)

143 ga 30


“Cyclic alkenylsulfonyl fluorides: Palladium-catalyzed synthesis and functionalization of compact multi-functional reagents”, Terry Shing-Bong Lou, Scott W. Bagley, and Michael C. Willis, Angew. Chem. Int. Ed201958, 18859-18863. (doi: 10.1002/anie.201910871)

141 ga 30


“Nickel(II)-catalyzed synthesis of sulfinates from aryl and heteroaryl boronic acids and the sulfur dioxide surrogate DABSO”, Pui Kin Tony Lo, Yiding Chen, Michael C. Willis, ACS Catalysis20199, 10668−10673. (doi: 10.1021/acscatal.9b04363)

142 ga 30


“Modular sulfondiimine synthesis using a stable sulfinylamine reagent”, Ze-Xin Zhang, Thomas Q. Davies, and Michael C. Willis, J. Am. Chem. Soc2019141, 13022−13027. (doi: 10.1021/jacs.9b06831)

140 ga 30


“New catalytic reactions using sulfur dioxide”, Michael C. Willis, Phosphorus, Sulfur, Silicon and the Related Elements 2019194,  654-657. (doi: 10.1080/10426507.2019.1602623)

139 ga 30


“A rhodium-catalysed Sonogashira-type coupling exploiting C-S functionalisation: Orthogonality with palladium-catalysed variants”, Milan Arambasic, Manjeet K. Majhail, Robert N. Straker, James D. Neuhaus and Michael C. Willis, Chem. Commun201955, 2757–2760. (doi: 10.1039/c9cc00092e)

138 ga 25


“Rhodium(I)-catalyzed hydroacylation”, Maitane Fernández and Michael C. Willis, in Rhodium catalysis in organic synthesis: Methods and reactions, edited by Ken Tanaka, Wiley-VCH, 2019, pp 63-84. (doi: 10.1002/9783527811908.ch4)

137 ga 15