53784-82-0Relevant articles and documents
Takeo et al.
, p. 111,114,116 (1974)
Synthesis of new series of α-cyclodextrin esters as dopamine carrier molecule
Seyedi, Seyed Mohammad,Sadeghian, Hamid,Jabbari, Atena,Assadieskandar, Amir,Momeni, Hamideh
, p. 4307 - 4311 (2011)
A new series of amphiphilic α-cyclodextrins were synthesized by grafting N-acylated amino acids [valine, leucine, phenylalanine, methionine, and tryptophan (3a-e)] to the primary hydroxyl groups via ester bond formation. The synthetic pathway involves sel
Precise Rate Control of Pseudorotaxane Dethreading by pH-Responsive Selectively Functionalized Cyclodextrins
Cherraben, Sawsen,Scelle, Jérémy,Hasenknopf, Bernold,Vives, Guillaume,Sollogoub, Matthieu
supporting information, p. 7938 - 7942 (2021/10/20)
A family of cyclodextrins functionalized with zero, one, two, or six amines was shown to control the rate of their threading and dethreading on a molecular axle depending on the pH and their substitution pattern. The originality of this system lies in the rate control of the switch by operating the stimulus directly on the macrocycle.
