Abstract
New sterically hindered functionalized o-quinones were synthesized by the 1,4-nucleophilic addition of secondary cyclic amines to 3,6-di(tert-butyl)-o-benzoquinone. The ability of these o-quinones to form o-semiquinone complexes with transition and main-group metals was studied by ESR spectroscopy in solution.
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1786–1793, September, 2007.
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Abakumov, G.A., Cherkasov, V.K., Kocherova, T.N. et al. Functionalization of sterically hindered o-benzoquinones: amino-substituted 3,6-di(tert-butyl)-o-benzoquinones. Russ Chem Bull 56, 1849–1856 (2007). https://doi.org/10.1007/s11172-007-0287-6
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DOI: https://doi.org/10.1007/s11172-007-0287-6