Michael C Willis

Summary

Affiliation: University of Oxford
Country: UK

Publications

  1. doi request reprint Tandem inverse-electron-demand hetero-/retro-Diels-Alder reactions for aromatic nitrogen heterocycle synthesis
    Radleigh A A Foster
    Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, OX1 3TA, UK
    Chem Soc Rev 42:63-76. 2013
  2. doi request reprint Palladium-catalysed aminosulfonylation of aryl-, alkenyl- and heteroaryl halides: scope of the three-component synthesis of N-aminosulfonamides
    Edward J Emmett
    Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, OX1 3TA, UK
    Org Biomol Chem 10:4007-14. 2012
  3. ncbi request reprint Palladium-catalyzed aminosulfonylation of aryl halides
    Bao Nguyen
    Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford OX1 3TA, UK
    J Am Chem Soc 132:16372-3. 2010

Collaborators

  • Edward J Emmett
  • Bao Nguyen
  • Radleigh A A Foster
  • Barry R Hayter
  • Charlotte S Richards-Taylor
  • Alfonso García-Rubia

Detail Information

Publications3

  1. doi request reprint Tandem inverse-electron-demand hetero-/retro-Diels-Alder reactions for aromatic nitrogen heterocycle synthesis
    Radleigh A A Foster
    Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, OX1 3TA, UK
    Chem Soc Rev 42:63-76. 2013
    ..In this tutorial review we discuss the range of commonly used dienophiles and aza-dienes for this process whilst highlighting the reactivity trends, and illustrating their applications...
  2. doi request reprint Palladium-catalysed aminosulfonylation of aryl-, alkenyl- and heteroaryl halides: scope of the three-component synthesis of N-aminosulfonamides
    Edward J Emmett
    Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, OX1 3TA, UK
    Org Biomol Chem 10:4007-14. 2012
    ..The ability to employ hydrazine·SO(2) complexes as both the N-nucleophile and SO(2) source is also illustrated...
  3. ncbi request reprint Palladium-catalyzed aminosulfonylation of aryl halides
    Bao Nguyen
    Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford OX1 3TA, UK
    J Am Chem Soc 132:16372-3. 2010
    ..The colorless crystalline solid DABCO·(SO(2))(2) was used as a convenient source of sulfur dioxide. The reaction tolerates significant variation of both the aryl iodide and hydrazine coupling partners...