ja8b09851_si_002.cif (9.73 MB)

Radical Germylzincation of α‑Heteroatom-Substituted Alkynes

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posted on 29.11.2018, 00:00 by Karen de la Vega-Hernández, Elise Romain, Anais Coffinet, Kajetan Bijouard, Geoffrey Gontard, Fabrice Chemla, Franck Ferreira, Olivier Jackowski, Alejandro Perez-Luna
The regio- and stereoselective addition of germanium and zinc across the C–C triple bond of nitrogen-, sulfur-, oxygen-, and phosphorus-substituted terminal and internal alkynes is achieved by reaction with a combination of R3GeH and Et2Zn. Diagnostic experiments support a radical-chain mechanism and the β-zincated vinylgermanes that show exceptional stability are characterized by NMR spectroscopy and X-ray crystallography. The unique feature of this new radical germylzincation reaction is that the C­(sp2)–Zn bond formed remains available for subsequent in situ Cu­(I)- or Pd(0)-mediated C–C or C–heteroatom bond formation with retention of the double bond geometry. These protocols offer modular access to elaborated tri- and tetrasubstituted vinylgermanes decorated with heteroatom substituents β to germanium that are useful for the preparation of stereodefined alkenes.

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