Synthesis and Characterization of Per‐3,6‐anhydro Cyclodextrins

Peter R. Ashton; Paul Ellwood; Ian Staton; J. Fraser Stoddart

doi:10.1002/anie.199100801

Synthesis and Characterization of Per‐3,6‐anhydro Cyclodextrins

Peter R. Ashton, Paul Ellwood, Ian Staton, J. Fraser Stoddart^*

^*Corresponding author for this work

Chemistry

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

56 Scopus citations

Abstract

Cyclodextrin derivatives such as 1, which contain glucopyranose units in ¹C₄ conformation, were synthesized from per(6‐O‐tosyl)‐β‐cyclodextrin. The pure α‐cyclodextrin derivative (with six sugar units) was obtained from per(2,3‐O‐benzoyl‐6‐O‐tosyl)‐α‐cyclodextrin. Both anhydrodextrins are potential molecular receptors in which the cavity is lined with hydroxyl groups. (Figure Presented.)

Original language	English (US)
Pages (from-to)	80-81
Number of pages	2
Journal	Angewandte Chemie International Edition in English
Volume	30
Issue number	1
DOIs	https://doi.org/10.1002/anie.199100801
State	Published - Jan 1991

ASJC Scopus subject areas

Catalysis
General Chemistry

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title = "Synthesis and Characterization of Per‐3,6‐anhydro Cyclodextrins",

abstract = "Cyclodextrin derivatives such as 1, which contain glucopyranose units in 1C4 conformation, were synthesized from per(6‐O‐tosyl)‐β‐cyclodextrin. The pure α‐cyclodextrin derivative (with six sugar units) was obtained from per(2,3‐O‐benzoyl‐6‐O‐tosyl)‐α‐cyclodextrin. Both anhydrodextrins are potential molecular receptors in which the cavity is lined with hydroxyl groups. (Figure Presented.)",

author = "Ashton, {Peter R.} and Paul Ellwood and Ian Staton and Stoddart, {J. Fraser}",

year = "1991",

month = jan,

doi = "10.1002/anie.199100801",

language = "English (US)",

volume = "30",

pages = "80--81",

journal = "Angewandte Chemie International Edition in English",

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T1 - Synthesis and Characterization of Per‐3,6‐anhydro Cyclodextrins

AU - Ashton, Peter R.

AU - Ellwood, Paul

AU - Staton, Ian

AU - Stoddart, J. Fraser

PY - 1991/1

Y1 - 1991/1

N2 - Cyclodextrin derivatives such as 1, which contain glucopyranose units in 1C4 conformation, were synthesized from per(6‐O‐tosyl)‐β‐cyclodextrin. The pure α‐cyclodextrin derivative (with six sugar units) was obtained from per(2,3‐O‐benzoyl‐6‐O‐tosyl)‐α‐cyclodextrin. Both anhydrodextrins are potential molecular receptors in which the cavity is lined with hydroxyl groups. (Figure Presented.)

AB - Cyclodextrin derivatives such as 1, which contain glucopyranose units in 1C4 conformation, were synthesized from per(6‐O‐tosyl)‐β‐cyclodextrin. The pure α‐cyclodextrin derivative (with six sugar units) was obtained from per(2,3‐O‐benzoyl‐6‐O‐tosyl)‐α‐cyclodextrin. Both anhydrodextrins are potential molecular receptors in which the cavity is lined with hydroxyl groups. (Figure Presented.)

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Synthesis and Characterization of Per‐3,6‐anhydro Cyclodextrins

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