Matteson Homologation

  • D. S. Matteson, "Boronic Esters in Stereodirected Synthesis", Tetrahedron 1989, 45, 1859–1885.
  • D. S. Matteson, "Boronic Esters in Asymmetric Synthesis", J. Org. Chem. 2013, 78, 10009–10023.
  • J. Gorges, U. Kazmaier, "Matteson Homologation-based Total Synthesis of Lagunamide A", Org. Lett. 2018, 20, 2033−2036.
  • O. Andler, U. Kazmaier, "A straightforward synthesis of polyketides via ester dienolate Matteson homologation", Chem. Eur. J. 2021, 27, 949–953. DOI: 10.1002/chem.202004650.
  • O. Andler, U. Kazmaier, "Total Synthesis of Apratoxin A and B using Matteson´s Homologation Approach", Org. Biomol. Chem. 2021, 19, 4866–4870. DOI: 10.1039/d1ob00713k.
  • O. Andler, U. Kazmaier, "Application of Allylzinc Reagents as Nucleophiles in Matteson Homologations", Org. Lett. 2021, 23, 8439–8444. DOI: 10.1021/acs.orglett.1c03164.
  • M. Tost, O. Andler, U. Kazmaier, "A Matteson homologation-based synthesis of doliculide and derivatives", Eur. J. Org. Chem. 2021, 6459–6471. DOI: 10.1002/ejoc.202101345.
  • O. Andler, U. Kazmaier, "Stereoselective Synthesis of a Protected Side Chain of Meliponamycin A", Org. Lett. 2022, 24, 2541−2545. DOI: 10.1021/acs.orglett.2c00701.
  • T. Kinsinger, U. Kazmaier, "Application of Vinyl Nucleophiles in Matteson Homologations", Org. Lett. 2022, 24, 3599−3603. DOI: 10.1021/acs.orglett.2c01119.
  • T. Kinsinger, U. Kazmaier, “Matteson Homologation of Arylboronic Esters”, Eur. J. Org. Chem.  2022, e202200625. DOI: 10.1002/ejoc.202200625.
  • T. Kinsinger, U. Kazmaier, “Combining Matteson Homologations and Claisen Rearrange­ments - An Efficient Tool for Amino Acid Synthesis”,  Eur. J. Org. Chem. 2022, e202201345. DOI: 10.1002/ejoc.202201345.