Javascript must be enabled to continue!
Mono-6-Substituted Cyclodextrins—Synthesis and Applications
View through CrossRef
Cyclodextrins are well known supramolecular hosts used in a wide range of applications. Monosubstitution of native cyclodextrins in the position C-6 of a glucose unit represents the simplest method how to achieve covalent binding of a well-defined host unit into the more complicated systems. These derivatives are relatively easy to prepare; that is why the number of publications describing their preparations exceeds 1400, and the reported synthetic methods are often very similar. Nevertheless, it might be very demanding to decide which of the published methods is the best one for the intended purpose. In the review, we aim to present only the most useful and well-described methods for preparing different types of mono-6-substituted derivatives. We also discuss the common problems encountered during their syntheses and suggest their optimal solutions.
Title: Mono-6-Substituted Cyclodextrins—Synthesis and Applications
Description:
Cyclodextrins are well known supramolecular hosts used in a wide range of applications.
Monosubstitution of native cyclodextrins in the position C-6 of a glucose unit represents the simplest method how to achieve covalent binding of a well-defined host unit into the more complicated systems.
These derivatives are relatively easy to prepare; that is why the number of publications describing their preparations exceeds 1400, and the reported synthetic methods are often very similar.
Nevertheless, it might be very demanding to decide which of the published methods is the best one for the intended purpose.
In the review, we aim to present only the most useful and well-described methods for preparing different types of mono-6-substituted derivatives.
We also discuss the common problems encountered during their syntheses and suggest their optimal solutions.
Related Results
Natural and synthetic cavitands: Challenges in chemistry and pharmaceutical technology
Natural and synthetic cavitands: Challenges in chemistry and pharmaceutical technology
<span>Supramolecular chemistry involves non-covalent interactions and specific molecular recognition of molecules/analytes by host molecules or supramolecules. These events a...
Cyclodextrins as Bricks for Tuning Polymer Properties
Cyclodextrins as Bricks for Tuning Polymer Properties
Cyclodextrins are natural cyclic oligosaccharides with a cone shape delimiting a hydrophobic cavity. The rims of cyclodextrins can be functionalized in order to improve their prope...
Encapsulation of benzene carboxylic acids using cyclodextrins
Encapsulation of benzene carboxylic acids using cyclodextrins
The encapsulation of medicinal substances in various polymers is a common way to increase their thermal, hydrolytic, and chemical stability. However, the bioavailability of the enc...
A review of mono- and bispecific genera of Amphibians worldwide
A review of mono- and bispecific genera of Amphibians worldwide
Monospecific and bispecific genera are of particular interest in studies of taxonomic diversity and speciation evolution. Here, the distribution patterns of mono- and bispecific am...
Cyclodextrins: An Overview of Fundamentals, Types, and Applications
Cyclodextrins: An Overview of Fundamentals, Types, and Applications
Cyclodextrins are one of the most interesting pharmaceutical excipients with substantial theoretical and applied impacts in pharmaceutical industry. Even though the chemical founda...
Cyclodextrins: Only Pharmaceutical Excipients or Full-Fledged Drug Candidates?
Cyclodextrins: Only Pharmaceutical Excipients or Full-Fledged Drug Candidates?
Cyclodextrins, representing a versatile family of cyclic oligosaccharides, have extensive pharmaceutical applications due to their unique truncated cone-shaped structure with a hyd...
A Novel Preparation and Purification of Ethyl-β-Cyclodextrins
A Novel Preparation and Purification of Ethyl-β-Cyclodextrins
Ethyl-β-cyclodextrin can be widely used for controlled release of drugs, but its application is greatly limited due to the use of toxic ethylation reagents such as diethyl sulfate,...
Design, Molecular Modeling and Synthesis of Some New Purine-diones and Pyridopyrimidine-diones with Anticancer Activity
Design, Molecular Modeling and Synthesis of Some New Purine-diones and Pyridopyrimidine-diones with Anticancer Activity
An olomoucine analogues of 2-[(1-substituted)-2,6-dioxo-2,3,6,7–tetrahydro-1H-purin-8-ylsulfanyl]-N-substituted acetamide 6a-g and 7a-g, 1-substituted-8-[2-(4-substituted phenyl)...

