Ronald C.D. Breslow (1931–2017)
Reviewed herein are key research accomplishments of Professor Ronald Charles D. Breslow (1931–2017) throughout his more than 60 year research career.
Tag: Synthesis
Synthesis and biological evaluation of novel β-cyclodextrin-fluvastatin conjugates
Drugs that may regulate lipid metabolism and lower cholesterol, such as statins (drugs that reduce de novo cholesterol synthesis) or
Meet the Experts: Cyclodextrins as active ingredients in the 21st century – Webinar of CycloLab
After the great success of the webinar held in May, 2021 a next webinar organized by CycloLab will be held
Single Isomer N-Heterocyclic Cyclodextrin Derivatives as Chiral Selectors in Capillary Electrophoresis
In order to better understand the chiral recognition mechanisms of positively charged cyclodextrin (CD) derivatives, the synthesis, the pKa determination by 1H
A review on mono-6 substituted cyclodextrins
The huge literature on synthesis and applications of mono-6-substituted CDs has been reviewed by Kasal and Jindrich selecting the most
Synthesis of cyclodextrin‐based radial polycatenane cyclized by amide bond and subsequent fabrication of water‐soluble derivatives
CD-based radial polycatenanes were prepared in one-pot through polypseudorotaxane formation between β-CD and thiolated pluronic and subsequent cyclization via disulfide
Hepta-differentiated beta-cyclodextrin was obtained through a programmed synthesis
Precise heterofunctionalisation of cyclodextrins is a well-known bottleneck in the chemistry of cyclodextrins. In fact, although many applications of cyclodextrins
Cyclodextrin dimers: a versatile approach to optimizing encapsulation and their application to therapeutic extraction of toxic oxysterols
A novel class of specifically engineered, dimerized cyclodextrin nanostructures was developed for the encapsulation of toxic biomolecules such as 7-ketocholesterol
Gd(3+) Complexes Conjugated to Cyclodextrins
In the search for improvement in the properties of gadolinium-based contrast agents, cyclodextrins (CDs) are interesting hydrophilic scaffolds with high
β-Cyclodextrin encapsulation of synthetic AHLs: drug delivery implications and quorum-quenching exploits
Many bacteria, such as Pseudomonas aeruginosa, regulate phenotypic switching in a population density-dependent manner through a phenomenon known as quorum