0000000000237375

AUTHOR

Dagmar Kraft

showing 7 related works from this author

Double and triple calix[4]arenis connected via the oxygen functions

1990

New macrocyclic molecules are described containing two or three p-tert-butylcalix[4]arene subunits connected via their oxygen atoms. These macrocycles are available by two general methods which are capable of producing assemblies with bridges of varying rigidity and length.

chemistry.chemical_classificationChemistryOrganic Chemistrychemistry.chemical_elementIR-70679PhotochemistryBiochemistryOxygenchemistry.chemical_compoundRigidity (electromagnetism)Polycyclic compoundDrug DiscoveryPolymer chemistryCalixareneMoleculePhenolsLactoneCyclophaneTetrahedron letters
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Regioselective synthesis of calixcrowns derived from p-tert-butylcalix[5]arene

1993

Abstract Alkylation of p-tert-butylcalix[5]arene with oligoethylene glycol-ditosylates in the presence of CsF affords the 1,3-bridged calix[5]crowns 1a–c in 51 to 72% yield. In the case of hexaethylene glycol the isomeric 1,2-bridged calix[5]crown-7 2c was obtained additionally. The calixcrowns were further modified by alkylation of the remaining hydroxyl groups.

chemistry.chemical_classificationStereochemistryOrganic ChemistryRegioselectivityAlkylationBiochemistryMedicinal chemistrychemistry.chemical_compoundPolycyclic compoundchemistryYield (chemistry)Drug DiscoveryCalixareneHexaethylene glycolCyclophaneTetrahedron
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ChemInform Abstract: Inherently Chiral Calixarenes

2010

ChemistryCalixareneGeneral MedicineCombinatorial chemistryChemInform
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Inherently Chiral Calixarenes

1994

Due to the nonplanarity of the basic 1 n -metacyclophane system, calixarenes and resorcarenes can be transformed into molecules with inherent chirality. Various attempts to achieve this goal are reviewed. Special emphasis is given to derivatives with C n -symmetry, including derivatives of spherand calixarenes and other calixarene-like macrocycles.

Computational chemistryChemistryCalixareneOrganic chemistryMoleculeInherent chiralitySymmetry (physics)
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Calix[4]arenes bridged at the lower rim

1990

Calix[41 arenes, in which two opposite p-positions are linked by an aliphatic chain, and their derivatives show transport or complexation properties strongly dependent on the length of this chain. Bicyclo-calix[4]arenes, a special case of 1,3-bridged calix[41 arenes, and annelated calix[41 arenes, a special case of 1 ,&bridged calix [4] arenes, are also described. Although the preferred conformation of calix[4]arenes is the coneconformation due to its stabilization by a cyclic array of hydrogen bonds between the phenolic hydroxyl goups, these molecules are flexible, with a cone to cone inversion rate of about 150 8-1 for a calix[glarene at 47OC (ref. 1). The cone (or any other) conformation…

chemistry.chemical_compoundchemistryRing flipHydrogen bondStereochemistryOrganic ChemistryCalixareneSulfonyl halideMoleculeIR-93402PhenolsMedicinal chemistryCyclophaneThe Journal of Organic Chemistry
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ChemInform Abstract: New Crown Ether-Like Macrocycles Containing a Nitrophenol Unit. Synthesis and Metal Ion Effects on the Reactivity of Their Aceta…

2010

chemistry.chemical_classificationMetalNitrophenolchemistry.chemical_compoundTransacylationchemistryvisual_artPolymer chemistryvisual_art.visual_art_mediumReactivity (chemistry)General MedicineCrown etherChemInform
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ChemInform Abstract: Regioselective Synthesis of Calixcrowns Derived from p-tert-Butylcalix( 5)arene.

2010

ChemistryRegioselectivityGeneral MedicineMedicinal chemistryChemInform
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