Abstract
Two methods for the synthesis of previously unavailable 1-substituted semithioglycolurils were developed. These methods consist of the cyclocondensation of 1-substituted ureas with 4,5-dihydroxy- or 4,5-dimethoxyimidazolidine-2-thione or glyoxal, followed by the reaction of the resulting 1-substituted 4,5-dihydroxyimidazolidine-2-ones with HSCN in a two-step one-pot procedure. Two of the desired semithioglycolurils were obtained as conglomerates.
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CITATION STYLE
Baranov, V. V., Galochkin, A. A., Nelyubina, Y. V., Kravchenko, A. N., & Makhova, N. N. (2020). Synthesis and Structure of 1-Substituted Semithioglycolurils. Synthesis (Germany), 52(17), 2563–2571. https://doi.org/10.1055/s-0040-1707391
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