Isomers of 3-(4-nitrophenyl)acrolein oxime

Journal Article · Tue Jun 10 00:00:00 EDT 1986 · J. Org. Chem. USSR (Engl. Transl.); (United States)

OSTI ID:6387776

Leitis, L Ya; Liepin'sh, E E; Yansone, D P; Dreibante, I I; Shimanskaya, M V; Maslii, L K; Nikol'skaya, G S

The Z and E isomers of 3-(4-nitrophenyl)acrolein oxime were obtained and characterized. The assignment was made on the basis of the geminal hetero constants /sup 2/J(/sup 15/N = C-/sup 1/H) and /sup 2/J(/sup 15/N = C-/sup 13/C).

• Research Organization: Institute of Organic Synthesis, Riga, USSR
• OSTI ID: 6387776
• Journal Information: J. Org. Chem. USSR (Engl. Transl.); (United States), Vol. 22:1; Other Information: Translated from Zh. Org. Khim.; 22: No.1, 64-65(Jan 1986)
• Country of Publication: United States
• Language: English

Related Subjects

37 INORGANIC
ORGANIC
PHYSICAL AND ANALYTICAL CHEMISTRY
74 ATOMIC AND MOLECULAR PHYSICS
ACROLEIN
ISOMERIZATION
ISOMERS
HYPERFINE STRUCTURE
NMR SPECTRA
NITRO COMPOUNDS
OXIMES
CARBON 13
CHEMICAL REACTION YIELD
CHEMICAL SHIFT
CONFORMATIONAL CHANGES
COUPLING CONSTANTS
DEUTERIUM COMPOUNDS
DMSO
ELECTRONIC STRUCTURE
HYDROGEN 1
INFRARED SPECTRA
J-J COUPLING
NITROGEN 15
STEREOCHEMISTRY
THIN-LAYER CHROMATOGRAPHY
VIBRATIONAL STATES
ALDEHYDES
AMINES
CARBON ISOTOPES
CHEMICAL REACTIONS
CHROMATOGRAPHY
COUPLING
ENERGY LEVELS
EVEN-ODD NUCLEI
EXCITED STATES
HYDROGEN COMPOUNDS
HYDROGEN ISOTOPES
HYDROXY COMPOUNDS
INTERMEDIATE COUPLING
ISOTOPES
LIGHT NUCLEI
NITROGEN ISOTOPES
NUCLEI
ODD-EVEN NUCLEI
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC SULFUR COMPOUNDS
SEPARATION PROCESSES
SPECTRA
STABLE ISOTOPES
SULFOXIDES
YIELDS
400201* - Chemical & Physicochemical Properties
640302 - Atomic
Molecular & Chemical Physics- Atomic & Molecular Properties & Theory