Proton and carbon-13 NMR studies of the phencyclone adducts of medium alkyl chain-length N-n-alkylmaleimides. Hindered rotations and magnetic anisotropic effects. Ab initio calculations for optimized structures

Spectroscopy Letters

Volumn 37, Issue 5, 2004, Pages 493-516

  Sklyut, Olga ^a   Prip, Ron ^a   Azar, Nikolay ^a   Callahan, Ronald ^b   Rothchild, Robert ^a,c  

^a JOHN JAY COLLEGE OF CRIMINAL JUSTICE   (United States)

^b NEW YORK UNIVERSITY   (United States)

^c CITY UNIVERSITY OF NEW YORK   (United States)

Author keywords

1H and 13C NMR; COSY; Dynamic NMR; Hartree Fock 6 31G*; Homonuclear chemical shift correlation NMR; Maleamic acids; Maleimides; One and two dimensional NMR; Restricted rotation; Stereochemistry

Indexed keywords

ACETONE; ALIPHATIC AMINE; ALKADIENE; ALKYL GROUP; BENZENE DERIVATIVE; DECYLMALEAMIC ACID; DECYLMALEIMIDE; DODECYLMALEAMIC ACID; DODECYLMALEIMIDE; HEPTYLMALEAMIC ACID; HEPTYLMALEIMIDE; MALEIC ANHYDRIDE; MALEIMIDE DERIVATIVE; NONYLMALEAMIC ACID; NONYLMALEIMIDE; OCTYLMALEAMIC ACID; OCTYLMALEIMIDE; PHENCYCLONE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; SOLVENT; UNCLASSIFIED DRUG;

AB INITIO CALCULATION; ANISOTROPY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; DIELS ALDER REACTION; ENVIRONMENTAL TEMPERATURE; GEOMETRY; MOLECULAR MODEL; PROTON NUCLEAR MAGNETIC RESONANCE; ROTATION; STEREOCHEMISTRY;

EID: 5144224414     PISSN: 00387010     EISSN: None     Source Type: Journal    
DOI: 10.1081/SL-120039699     Document Type: Article

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