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Synthesis and /sup 1/H and /sup 31/P NMR spectral characteristics of 2-substituted and 2,2-disubstituted 5-phenyl-5-thio-1,3,5-dioxaphosphorinanes

Journal Article · · Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States)
DOI:https://doi.org/10.1007/BF00959386· OSTI ID:5737043
The authors have studied the reactions of phenylbis(hydroxymethyl)phosphine sulfide (PHPS) with acetals and ketals. /sup 31/P NMR Spectra were recorded at 10.2 HMz on a KGU-4 spectrometer with proton noise decoupling at 25.2 MHz. Chemical shifts are given relative to 85% H/sub 3/PO/sub 4/ (negative values to higher field). PMR Spectra were measured on a Varian T60 machine at 34.5/sup 0/C. Treatment of phenylbis(hydroxymethyl)phosphine sulfide with acetals and ketals gives the corresponding 2-substituted and 2,2-disubstituted 5-phenyl-5-thio-1,3,5-dioxaphosphorinanes in which the P-Phenyl substituent occupies an axial position.
Research Organization:
A.E. Arbuzov Institute of Organic and Physical Chemistry, Kazan, USSR
OSTI ID:
5737043
Journal Information:
Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States), Journal Name: Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States) Vol. 36:2; ISSN BACCA
Country of Publication:
United States
Language:
English