2022
“A modular two-step route to sulfondiimidamides”, Ze-Xin Zhang, Charles Bell, Mingyan Ding, Michael C. Willis, J. Am. Chem. Soc. 2022, 144, 11851−11858. (doi: 10.1021/jacs.2c04404).
"Photocatalytic late‑stage functionalization of sulfonamides via Sulfonyl Radical Intermediates", Michael J. Tilby, Damien F. Dewez, Loїc R. E. Pantaine, Adrian Hall, Carolina Martínez-Lamenca, Michael C. Willis, ACS Catalysis, 2022, 12, 6060−6067. (doi: 10.1021/acscatal.2c01442).
“Sulfondiimidamides as new functional groups for synthetic and medicinal chemistry”, Ze-Xin Zhang and Michael C. Willis, Chem 2022, 8, 1137–1146. (doi: 10.1016/j.chempr.2022.02.013).
"Reductant-Free Cross-Electrophile Synthesis of Di(hetero)arylmethanes by Palladium-Catalyzed Desulfinative C–C Coupling", Janette McKnight, Andre Shavnya, Neal W. Sach] David C. Blakemore, Ian B. Moses, and Michael C. Willis, Angewandte. Chem. Int. Ed. 2022, 61, e202116775. (doi: 10.1002/anie.202116775)
“A silyl sulfinylamine reagent enables the modular synthesis of sulfonimidamides via primary sulfinamides”, Mingyan Ding, Ze-Xin Zhang, Thomas Q. Davies, and Michael C. Willis, Org. Lett. 2022, 24, 1711-1715. (doi: 10.1021/acs.orglett.2c00347)
"DABSO – A reagent to revolutionize organosulfur chemistry", Jonathan A. Andrews and Michael C. Willis, Synthesis 2022, 54. (doi: 10.1055/s-0040-1719864)
"Sulfonyl fluorides as targets and substrates in the development of new synthetic methods", Terry Shing-Bong Lou and Michael C. Willis, Nat. Rev. Chem. 2022, 6. (doi: 10.1038/s41570-021-00352-8)
"Diverse saturated heterocycles from a hydroacylation/conjugate addition cascade", Ndidi U. N. Iwumene, Daniel. F. Moseley, Robert D. C. Pullin and Michael C. Willis, Chem. Sci. 2022, 13, 1504–1511. (doi: 10.1039/d1sc06900d)
