New methods of modification of α-cyclodextrin

Research output: Contribution to journal › Review › Research › peer-review

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New methods of modification of α-cyclodextrin. / Özcan, Bilge Deniz; Zimmermann, Morten Lang; Ren, Mingzhe; Bols, Mikael.

In: Organic and Biomolecular Chemistry, Vol. 22, No. 35, 2024, p. 7092–7102.

Research output: Contribution to journal › Review › Research › peer-review

Harvard

Özcan, BD, Zimmermann, ML, Ren, M & Bols, M 2024, 'New methods of modification of α-cyclodextrin', Organic and Biomolecular Chemistry, vol. 22, no. 35, pp. 7092–7102. https://doi.org/10.1039/d4ob01109k

APA

Özcan, B. D., Zimmermann, M. L., Ren, M., & Bols, M. (2024). New methods of modification of α-cyclodextrin. Organic and Biomolecular Chemistry, 22(35), 7092–7102. https://doi.org/10.1039/d4ob01109k

Vancouver

Özcan BD, Zimmermann ML, Ren M, Bols M. New methods of modification of α-cyclodextrin. Organic and Biomolecular Chemistry. 2024;22(35):7092–7102. https://doi.org/10.1039/d4ob01109k

Author

Özcan, Bilge Deniz ; Zimmermann, Morten Lang ; Ren, Mingzhe ; Bols, Mikael. / New methods of modification of α-cyclodextrin. In: Organic and Biomolecular Chemistry. 2024 ; Vol. 22, No. 35. pp. 7092–7102.

Bibtex

@article{4c44bc14609b46dbad25e07c2747b6b6,

title = "New methods of modification of α-cyclodextrin",

abstract = "While being some of the oldest supramolecular hosts, cyclodextrins remain very popular as molecular binders in materials, devices, artificial enzymes and more. The popularity is undoubtedly connected to the ready availability, carbohydrate biomass origin, biodegradability and water solubility of the cyclodextrins. Many of these applications require synthetic modification of the cyclodextrin - at the simplest the attachment of a linker - but also often attachment of several functional groups, lids, bridges etc. Here we review state of the art methods of modifying α-cyclodextrin, which include direct modications of unprotected α-cyclodextrin and protection/deprotection method to partially modified cyclodextrins.",

author = "{\"O}zcan, {Bilge Deniz} and Zimmermann, {Morten Lang} and Mingzhe Ren and Mikael Bols",

note = "Publisher Copyright: {\textcopyright} 2024 The Royal Society of Chemistry.",

year = "2024",

doi = "10.1039/d4ob01109k",

language = "English",

volume = "22",

pages = "7092–7102",

journal = "Organic & Biomolecular Chemistry",

issn = "1470-4358",

publisher = "Royal Society of Chemistry",

number = "35",

}

RIS

TY - JOUR

T1 - New methods of modification of α-cyclodextrin

AU - Özcan, Bilge Deniz

AU - Zimmermann, Morten Lang

AU - Ren, Mingzhe

AU - Bols, Mikael

PY - 2024

Y1 - 2024

N2 - While being some of the oldest supramolecular hosts, cyclodextrins remain very popular as molecular binders in materials, devices, artificial enzymes and more. The popularity is undoubtedly connected to the ready availability, carbohydrate biomass origin, biodegradability and water solubility of the cyclodextrins. Many of these applications require synthetic modification of the cyclodextrin - at the simplest the attachment of a linker - but also often attachment of several functional groups, lids, bridges etc. Here we review state of the art methods of modifying α-cyclodextrin, which include direct modications of unprotected α-cyclodextrin and protection/deprotection method to partially modified cyclodextrins.

AB - While being some of the oldest supramolecular hosts, cyclodextrins remain very popular as molecular binders in materials, devices, artificial enzymes and more. The popularity is undoubtedly connected to the ready availability, carbohydrate biomass origin, biodegradability and water solubility of the cyclodextrins. Many of these applications require synthetic modification of the cyclodextrin - at the simplest the attachment of a linker - but also often attachment of several functional groups, lids, bridges etc. Here we review state of the art methods of modifying α-cyclodextrin, which include direct modications of unprotected α-cyclodextrin and protection/deprotection method to partially modified cyclodextrins.

U2 - 10.1039/d4ob01109k

DO - 10.1039/d4ob01109k

M3 - Review

C2 - 39171533

AN - SCOPUS:85201879761

VL - 22

SP - 7092

EP - 7102

JO - Organic & Biomolecular Chemistry

JF - Organic & Biomolecular Chemistry

SN - 1470-4358

IS - 35

ER -

ID: 403321599

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