SynOpen, Table of Contents CC BY-NC-ND 4.0 · SynOpen 2022; 06(01): 16-18DOI: 10.1055/a-1737-8610 letter A Homocoupling Approach to the Key Dione of CyMe4-BTPhen – Vital Ligands for Nuclear Clean-Up by the SANEX Process Thomas M. Trunks , Jasraj Singh Babra , James Westwood , Christopher D. Smith ∗ Recommend Article Abstract All articles of this category Abstract CyMe4-BTPhen and CyMe4-BTBP are the principal ligand systems used in Europe for the separation of actinides from lanthanides as a part of the SANEX process for nuclear recycling and reprocessing. We present a new approach to the synthesis of the CyMe4 fragment beginning from readily available hydroxypivalic acid. It features a cobalt-catalysed homocoupling of a neopentyl bromide to provide the key bisester precursor, thereby avoiding the requirement for technically challenging low-temperature LDA-mediated aldol chemistries. Key words Key wordshomocoupling - catalysis - nuclear clean-up - elemental separations - SANEX process - accident tolerant fuel Full Text References References 1 Fuel Cycle Stewardship in a Nuclear Renaissance (October 2011), The Royal Society Science Policy Centre report 10/11, see (accessed Dec 21, 2021): https://royalsociety.org/~/media/royal_society_content/policy/projects/nuclear-non-proliferation/fuelcyclestewardshipnuclearrenaissance.pdf 2 Corkhill C, Hyatt N. Nuclear Waste Management . IOP Publishing; Bristol: 2018 3 Ekberg C, Fermvik A, Retegan T, Skarnemark G, Foreman MR. S, Hudson MJ, Englund S, Nilsson M. Radiochim. Acta 2008; 96 4 Dam HH, Reinhoudt DN, Verboom W. Chem. Soc. Rev. 2007; 36: 367 5 Kolarik Z. Chem. Rev. 2008; 108: 4208 6 Leoncini A, Huskens J, Verboom W. Chem. Soc. Rev. 2017; 46: 7229 7 Veliscek-Carolan J. J. Hazard. Mater. 2016; 318: 266 8 Bhattacharyya A, Mohapatra PK. Radiochim. Acta 2019; 107: 931 9 Lewis FW, Harwood LM, Hudson MJ, Drew MG. B, Desreux JF, Vidick G, Bouslimani N, Modolo G, Wilden A, Sypula M, Vu T.-H, Simonin J.-P. J. Am. Chem. Soc. 2011; 133: 13093 10 Lewis FW, Harwood LM, Hudson MJ, Drew MG. B, Modolo G, Sypula M, Desreux JF, Bouslimani N, Vidick G. Dalt. Trans. 2010; 39: 5172 11 Afsar A, Westwood J, Distler P, Harwood LM, Mohan S, John J, Davis FJ. Tetrahedron 2018; 74: 5258 12 Harwood LM, Afsar A, Distler P, John JS, Babra JY, Selfe Z, Cowell J, Westwood J. Heterocycles 2019; 99: 825 13 Magnusson D, Christiansen B, Foreman MR. S, Geist A, Glatz JP, Malmbeck R, Modolo G, Serrano Purroy D, Sorel C. Solvent Extr. Ion Exch. 2009; 27: 97 14 Wilden A, Modolo G, Schreinemachers C, Sadowski F, Lange S, Sypula M, Magnusson D, Geist A, Lewis FW, Harwood LM, Hudson MJ. Solvent Extr. Ion Exch. 2013; 31: 519 15 Magnusson D, Geist A, Wilden A, Modolo G. Solvent Extr. Ion Exch. 2013; 31: 1 16 Gulledge ZZ, Tedder ML, Lyons KR, Carrick JD. ACS Omega 2019; 4: 18855 17 Ebenezer C, Vijay Solomon R. Inorg. Chem. Front. 2021; 8: 3012 18 Waters GD, Carrick JD. RSC Adv. 2020; 10: 10807 19 Trumm S, Geist A, Panak PJ, Fanghänel T. Solvent Extr. Ion Exch. 2011; 29: 213 20 Greene JL, Hagemeyer HJ. J. Am. Chem. Soc. 1955; 77: 3016 21 Ahmed M, Giblin G, Martin P, Myatt J, Norton D, Rivers DA. WO2008128951A1, 2008 22 Grunwald E, Winstein S. J. Am. Chem. Soc. 1948; 70: 846 23 Wiedemann EN, Mandl FA, Blank ID, Ochsenfeld C, Ofial AR, Sieber SA. ChemPlusChem 2015; 80: 1673 24 Robinson SL, Christenson JK, Wackett LP. Nat. Prod. Rep. 2019; 36: 458 25 Jung ME, Piizzi G. Chem. Rev. 2005; 105: 1735 26 Kingsbury CA. J. Org. Chem. 1968; 33: 3247 27 Cai Y, Qian X, Gosmini C. Adv. Synth. Catal. 2016; 358: 2427 28 Goldup SM, Leigh DA, McBurney RT, McGonigal PR, Plant A. Chem. Sci. 2010; 1: 383 29 Collins PF, Diehl H, Smith GF. Anal. Chem. 1959; 31: 1862 30 Tungen JE, Aursnes M, Dalli J, Arnardottir H, Serhan CN, Hansen TV. Chem. Eur. J. 2014; 20: 14575 Supplementary Material Supplementary Material Supporting Information