Templated synthesis of glycoluril hexamer and monofunctionalized cucurbit[6]uril derivatives

Journal of the American Chemical Society

Volumn 133, Issue 44, 2011, Pages 17966-17976

  Lucas, Derick ^a   Minami, Tsuyoshi ^b   Iannuzzi, Greg ^a   Cao, Liping ^a   Wittenberg, James B ^a   Anzenbacher, Pavel ^b   Isaacs, Lyle ^a  

^a Bldg 142   (United States)

^b BOWLING GREEN STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIUM IONS; CUCURBIT[6]URIL; CUCURBIT[N]URIL; FUNCTIONALIZATION REACTIONS; GRAM SCALE; HEXAMERS; MACROCYCLIZATION REACTIONS; MACROCYLIZATION; MECHANISTIC PATHWAYS; ONE STEP; PARAFORMALDEHYDES; PHTHALALDEHYDE; ROOM TEMPERATURE; SYNTHETIC PROCEDURES; TEMPLATED SYNTHESIS;

ACETAL RESINS; AMMONIUM COMPOUNDS; BINDING SITES; ENZYME INHIBITION; EUROPIUM; FLUOROPHORES; NAPHTHALENE; REACTION KINETICS; SYNTHESIS (CHEMICAL);

IONS;

4 XYLYLENEDIAMMONIUM ION; AMMONIUM DERIVATIVE; CHEMICAL COMPOUND; CUCURBIT[6]URIL DERIVATIVE; FORMALDEHYDE; GLYCOLURIL HEXAMER; HEXANEDIAMMONIUM ION; PARAFORMALDEHYDE; PHTHALALDEHYDE; POLYMER; UNCLASSIFIED DRUG;

ARTICLE; BINDING KINETICS; CHEMICAL REACTION KINETICS; CYCLIZATION; FLUORESCENCE ANALYSIS; MACROCYCLIZATION; ROOM TEMPERATURE; SYNTHESIS; TEMPLATED SYNTHESIS; THERMODYNAMICS;

ALKYNES; BRIDGED COMPOUNDS; IMIDAZOLES; MODELS, MOLECULAR; MOLECULAR STRUCTURE;

EID: 80455167986     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja208229d     Document Type: Article

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