Carbamylphosphonates and Related Compounds—Nuclear-Magnetic-Resonance and Infrared Spectra

1967 ◽  
Vol 21 (1) ◽  
pp. 9-15 ◽  
Author(s):  
T. H. Siddall ◽  
C. A. Prohaska
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Infrared Spectra ◽  
Proton Magnetic Resonance ◽  
Structural Features ◽  
Slow Rotation ◽  
The Common ◽  
Related Compounds ◽  
Great Evidence ◽  
Nitrogen Bond

Proton magnetic resonance and infrared spectra were obtained for 44 carbamylphosphonates and related compounds, the common structural features being the grouping As with ordinary amides, slow rotation is observed around the carbonyl-to-nitrogen bond, but the chemical shift between nitrogen substituents is three to five times as great. Evidence is presented for long range coupling of phosphorus to protons in N-substituents. Correlations are observed between the carbonyl and phosphoryl stretching frequencies and substituents both on nitrogen and on phosphorus.

Spectra-Structure Correlations of Some Heterocyclic Pharmaceuticals

1965 ◽  
Vol 48 (3) ◽  
pp. 596-600
Author(s):  
Alma L Hayden ◽  
Millard Maienthal
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Infrared Spectra ◽  
Near Infrared ◽  
Magnetic Resonance Data ◽  
Structure Correlations ◽  
Group Frequency ◽  
Resonance Data ◽  
The Relationship ◽  
Related Compounds

Abstract The results of a study of the relationship between spectra and structure of zoxazolamine, methimazole, and some related compounds are presented. Group frequency assignments of the infrared spectra were clarified or confirmed by comparisons with ultraviolet, near infrared, and nuclear magnetic resonance data.

Investigation and Identification of the Bromination Products of Dimethoxyamphetamines

1976 ◽  
Vol 59 (5) ◽  
pp. 1162-1169
Author(s):  
Keith Bailey ◽  
Denise R Gagné ◽  
Richard K Pike
Keyword(s):  
Magnetic Resonance ◽  
Qualitative Analysis ◽  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Infrared Spectra ◽  
Proton Magnetic Resonance ◽  
Positive Identification ◽  
Aromatic Bromination ◽  
Layer Chromatography ◽  
Magnetic Resonance Spectra

Abstract The qualitative analysis of the aromatic bromination products of the 6 isomeric dimethoxyamphetamines and their hydrochloride or hydrobromide salts is described. Their ultraviolet, mass, and proton magnetic resonance spectra are not sufficiently different for distinction but infrared spectra allow a positive identification to be made and reference spectra are provided for the bromination products of 2,4-, 2,5-, 2,6-, 4,5-, and 3,5-dimethoxyamphetamines. The application of gas-liquid and thin layer chromatography for the analysis of these products is discussed. The bromination of 2,3-dimethoxyamphetamine consistently gave mixtures which could not be separated satisfactorily; spectra are included for completeness of the comparison of products.

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