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- W1565008001 abstract "A number of chiral racemic and enanthiopure thiophosphorylated thioureas were synthesized by the reaction of 2-aminobutan-1-ol and 1-(a-aminobenzyl)-2-naphthol with O,O-diethyl thiophosphoryl isothiocyanate. It was found that such thioureas undergo the cyclization reaction under basic conditions with hydrogen sulfide elimination and the formation of thiophosphorylated oxasines. X-Ray single crystal diffraction revealed that the structure of thiourea is close to the prereaction state of the cyclization reaction." @default.
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- W1565008001 date "2014-07-18" @default.
- W1565008001 modified "2023-10-18" @default.
- W1565008001 title "Chiral Thiophosphorylated Thioureas: Synthesis, Structure, and Cyclization Reaction" @default.
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- W1565008001 doi "https://doi.org/10.1002/hc.21202" @default.
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