Synthesis of ammonium substituted β-cyclodextrins for enantioseparation of anionic analytes

I. Wayan Muderawan; Teng Teng Ong; Wei Hua Tang; David J. Young; Chi Bun Ching; Siu Choon Ng

doi:10.1016/j.tetlet.2005.01.059

Synthesis of ammonium substituted β-cyclodextrins for enantioseparation of anionic analytes

I. Wayan Muderawan, Teng Teng Ong, Wei Hua Tang, David J. Young, Chi Bun Ching, Siu Choon Ng

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

Abstract

New ammonium functionalized cyclodextrins can be prepared in excellent yields by displacement of 6-tosyl-β-cyclodextrin with alkylimidazoles, pyridine or alkylamines and achieve excellent enantioseparation of dansyl amino acids presumably due to electrostatic interactions between the cationic host and anionic guest.

Original language	English
Pages (from-to)	1747-1749
Number of pages	3
Journal	Tetrahedron Letters
Volume	46
Issue number	10
DOIs	https://doi.org/10.1016/j.tetlet.2005.01.059
Publication status	Published - 7 Mar 2005
Externally published	Yes

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10.1016/j.tetlet.2005.01.059

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title = "Synthesis of ammonium substituted β-cyclodextrins for enantioseparation of anionic analytes",

abstract = "New ammonium functionalized cyclodextrins can be prepared in excellent yields by displacement of 6-tosyl-β-cyclodextrin with alkylimidazoles, pyridine or alkylamines and achieve excellent enantioseparation of dansyl amino acids presumably due to electrostatic interactions between the cationic host and anionic guest.",

keywords = "Cationic cyclodextrins, Enantiomeric resolution",

author = "Muderawan, {I. Wayan} and Ong, {Teng Teng} and Tang, {Wei Hua} and Young, {David J.} and Ching, {Chi Bun} and Ng, {Siu Choon}",

year = "2005",

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T1 - Synthesis of ammonium substituted β-cyclodextrins for enantioseparation of anionic analytes

AU - Muderawan, I. Wayan

AU - Ong, Teng Teng

AU - Tang, Wei Hua

AU - Young, David J.

AU - Ching, Chi Bun

AU - Ng, Siu Choon

PY - 2005/3/7

Y1 - 2005/3/7

N2 - New ammonium functionalized cyclodextrins can be prepared in excellent yields by displacement of 6-tosyl-β-cyclodextrin with alkylimidazoles, pyridine or alkylamines and achieve excellent enantioseparation of dansyl amino acids presumably due to electrostatic interactions between the cationic host and anionic guest.

AB - New ammonium functionalized cyclodextrins can be prepared in excellent yields by displacement of 6-tosyl-β-cyclodextrin with alkylimidazoles, pyridine or alkylamines and achieve excellent enantioseparation of dansyl amino acids presumably due to electrostatic interactions between the cationic host and anionic guest.

KW - Cationic cyclodextrins

KW - Enantiomeric resolution

UR - http://www.scopus.com/inward/record.url?scp=13744261937&partnerID=8YFLogxK

U2 - 10.1016/j.tetlet.2005.01.059

DO - 10.1016/j.tetlet.2005.01.059

M3 - Article

AN - SCOPUS:13744261937

VL - 46

SP - 1747

EP - 1749

JO - Tetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry

JF - Tetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry

SN - 0040-4039

IS - 10

ER -

Synthesis of ammonium substituted β-cyclodextrins for enantioseparation of anionic analytes

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