32860-56-3Relevant articles and documents
Application of host-guest chemistry in nanotube-based device fabrication: Photochemically controlled immobilization of azobenzene nanotubes on patterned α-CD monolayer/Au substrates via molecular recognition
Banerjee, Ipsita A.,Yu, Lingtao,Matsui, Hiroshi
, p. 9542 - 9543 (2003)
Azobenzene-functionalized nanotubes recognized and attached onto well-defined complementary regions of thiolated α-CD SAM/Au substrates via host-guest molecular recognition. The binding between the azobenzene nanotubes and the α-CD SAM/Au substrates was c
CONVENIENT PREPARATION AND EFFECTIVE SEPARATION OF THE C-2 AND C-3 TOSYLATES OF α-CYCLODEXTRIN
Fujita, Kahee,Nagamura, Satoru,Imoto, Taiji
, p. 5673 - 5676 (1984)
Secondary tosylates of α-cyclodextrin were conveniently prepared by the reaction of the cyclodextrin with tosyl chloride in alkaline water where pH of the mixture should be allowed to decrease as the proceeding of reaction, and were effectivelly separated by reversed-phase column chromatography.
Unraveling unidirectional threading of α-cyclodextrin in a [2]rotaxane through spin labeling approach
Casati, Costanza,Franchi, Paola,Pievo, Roberta,Mezzina, Elisabetta,Lucarini, Marco
, p. 19108 - 19117 (2012)
We present here the results of a CW-ESR investigation of a double spin labeled α-cyclodextrin-based [2]rotaxane that is characterized by the presence of nitroxide labels both at the wheel and at the dumbbell. This was accomplished by synthesizing a spin l
Synthesis and biological evaluation of multivalent carbohydrate ligands obtained by click assembly of pseudo-rotaxanes
Chwalek, Martin,Auzely, Rachel,Fort, Sebastien
, p. 1680 - 1688 (2009)
Multivalent carbohydrate ligands have been prepared by assembling α-cyclodextrin-based pseudo-rotaxanes through "click chemistry". The inclusion complex formed by a lactosyl-α-CD conjugate and a decane axle carrying a lactosyl stopper at one extremity and
CYCLODEXTRIN PROTEIN DRUG CONJUGATES
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Paragraph 0364, (2018/12/04)
Provided herein are compounds, compositions, conjugates and methods for the treatment of diseases, and/or conditions such as, but not limited to, proliferative diseases. In certain embodiments, compounds, compositions, and conjugates are provided, which include cyclodextrin-based linker-payloads and protein conjugates thereof, and/or in combination with other agents. By administering these compounds, compositions, and conjugates as described herein to specific target cells, side-effects due to non-specific binding phenomena, for example, to non-target cells are reduced.
Enhanced single-isomer separation and pseudoenantiomer resolution of new primary rim heterobifunctionalized α-cyclodextrin derivatives
Tichá, Iveta,Benkovics, Gábor,Malanga, Milo,Jind?ich, Jind?ich
supporting information, p. 2829 - 2837 (2018/11/27)
The synthesis of batch-to-batch reproducible cyclodextrin (CD) derivatives often requires functionalization at specific positions of the CD skeleton. However, the regioselective preparation of this type of CD derivatives remains a challenge in synthetic c
