1,3-Diiodocalix[4]arene: Synthesis by ullmann-type iodination of 1,3-bistriflate ester of calix[4]arene, conformational analysis, and transformation into 1,3-dicarboxy-, diformyl-, and dialkylcalix[4]arenes

Journal of Organic Chemistry

Volumn 80, Issue 2, 2015, Pages 1070-1081

  Tanaka, Shinya ^a   Umetsu, Takafumi ^a   Nebuya, Satoru ^a   Morohashi, Naoya ^a   Hattori, Tetsutaro ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATION ENERGY; CARBON DIOXIDE; ESTERIFICATION; ESTERS; FREE ENERGY; HALOGENATION; X RAY CRYSTALLOGRAPHY;

ACTIVATION FREE ENERGY; ANTI CONFORMERS; CONE CONFORMATIONS; CONFORMATIONAL ANALYSIS; COPPER CATALYZED; DICARBOXYLIC ACID; FACILE SYNTHESIS; P-TERT-BUTYLCALIX[4]ARENE;

CONFORMATIONS;

ALKYL GROUP; CALIXARENE; DICARBOXYLIC ACID; HYDROXYL GROUP; MACROCYCLIC COMPOUND; POLYCYCLIC AROMATIC HYDROCARBON; CALIX(4)ARENE; PHENOL DERIVATIVE;

ALKYLATION; ARTICLE; CONFORMATION; FORMYLATION; IODINATION; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOSPECIFICITY; SYNTHESIS; X RAY CRYSTALLOGRAPHY; CHEMISTRY; HALOGENATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

CALIXARENES; CRYSTALLOGRAPHY, X-RAY; HALOGENATION; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; PHENOLS;

EID: 84921341293     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo502563z     Document Type: Article

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