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Synthesis of 1,3,4-thiadiazaphospholes from 1-phenoxy-2-thiocyanatoethene

Journal Article · · J. Gen. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:5615528
1-Phenoxy-2-thiocyanatoethene undergoes reaction with phosphorus pentachloride with the participation of two reaction centers, vinyl and thiocyanate groups, to form a phosphorus-containing heterocycle, a derivative of 1,3,4-thiazaphosph-2-ole. Transformations of the phosphorylation product were studied. The /sup 1/H, /sup 31/P, and /sup 13/C NMR spectra were recorded on a WP-200SY Bruker spectrometer at room temperature. The stabilization was carried out with respect to a deuterium signal in CDCl/sub 3/. The /sup 31/P NMR signals were recorded relative to 85% H/sub 3/PO/sub 4/ as external standard (the positive values designate shift to the weak field) with a heteronuclear broadband uncoupling from protons.
OSTI ID:
5615528
Journal Information:
J. Gen. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Gen. Chem. USSR (Engl. Transl.); (United States) Vol. 57:3; ISSN JGCHA
Country of Publication:
United States
Language:
English

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