Conjugated macrocycles related to the porphyrins. 25. Proton NMR spectroscopic evidence for a preferred [18]annulene substructure in carbaporphyrins from the magnitude of selected 4JH,H CH=C-CH3 coupling constants

Journal of Organic Chemistry

Volumn 68, Issue 5, 2003, Pages 1755-1761

  Liu, Dachun ^a   Lash, Timothy D ^a  

^a ILLINOIS STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARBAPORPHYRIIN;

CHEMICAL BONDS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROTONS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

PORPHYRINS;

ANNULENE DERIVATIVE; CARBAPORPHYRIN; MACROCYCLIC COMPOUND; PORPHYRIN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; BINDING KINETICS; CHEMICAL ANALYSIS; CHEMICAL BOND; CHEMICAL STRUCTURE; LOW TEMPERATURE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 0037424321     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo020703u     Document Type: Article

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