Substituted heterocyclic naphthalene diimides with unexpected acidity. Synthesis, properties, and reactivity

Journal of Organic Chemistry

Volumn 74, Issue 22, 2009, Pages 8616-8625

  Doria, Filippo ^a   Di Antonio, Marco ^b   Benotti, Michele ^a   Verga, Daniela ^a   Freccero, Mauro ^a  

^a UNIVERSITY OF PAVIA   (Italy)

^b UNIVERSITY OF PADOVA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ACID CONDITIONS; AQUEOUS DMSO; AQUEOUS SOLVENTS; BROMINE ATOMS; CHEMICAL EQUATIONS; CYCLOHEXYL; GREEN EMISSIONS; HETEROCYCLES; IMIDIZATION; IN-SITU; NUCLEOPHILIC DISPLACEMENT; PCM MODEL; REDUCTIVE DEHALOGENATION; SPECIFIC SOLVATION; UV-VIS SPECTROSCOPY; WATER MOLECULE; WATER RATIO; WATER SOLUTIONS;

AMINES; BROMINE; DEHALOGENATION; DIMETHYL SULFOXIDE; ETHANE; ORGANIC SOLVENTS; SYNTHESIS (CHEMICAL); ULTRAVIOLET SPECTROSCOPY;

NAPHTHALENE;

BROMINE DERIVATIVE; CYCLOHEXANE DERIVATIVE; DIMETHYL SULFOXIDE; DYE; ETHYLENEDIAMINE; HETEROCYCLIC COMPOUND; IMIDE; NAPHTHALENE DERIVATIVE; ORGANIC SOLVENT; PYRAZINE DERIVATIVE;

ACID BASE BALANCE; ACIDITY; AQUEOUS SOLUTION; ARTICLE; CONJUGATE; DEHALOGENATION; DENSITY FUNCTIONAL THEORY; IMIDIZATION; OXIDATION; QUANTITATIVE ANALYSIS; REACTION ANALYSIS; REDUCTION; SOLVATION; SYNTHESIS; ULTRAVIOLET SPECTROSCOPY;

CRYSTALLOGRAPHY, X-RAY; HETEROCYCLIC COMPOUNDS; IMIDES; MODELS, MOLECULAR; MOLECULAR STRUCTURE; NAPHTHALENES;

EID: 70449674657     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9017342     Document Type: Article

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