The synthesis of a chiral receptor molecule containing three carbohydrate residues within a 20-crown-6 constitution

David G. Andrews; Peter R. Ashton; Dale A. Laidler; J. Fraser Stoddart; John B. Wolstenholme

doi:10.1016/S0040-4039(01)86369-3

The synthesis of a chiral receptor molecule containing three carbohydrate residues within a 20-crown-6 constitution

David G. Andrews, Peter R. Ashton, Dale A. Laidler, J. Fraser Stoddart^*, John B. Wolstenholme

^*Corresponding author for this work

Chemistry

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

11 Scopus citations

Abstract

The rationale behind designing and the approach to synthesising chiral crown ethers incorporating three trigonally-disposed carbohydrate residues is presented as a prelude to attaining chiral discrimination in the complexation of (R)- and (S)-α-phenylethylammonium perchlorate.

Original language	English (US)
Pages (from-to)	2629-2632
Number of pages	4
Journal	Tetrahedron Letters
Volume	20
Issue number	28
DOIs	https://doi.org/10.1016/S0040-4039(01)86369-3
State	Published - 1979

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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title = "The synthesis of a chiral receptor molecule containing three carbohydrate residues within a 20-crown-6 constitution",

abstract = "The rationale behind designing and the approach to synthesising chiral crown ethers incorporating three trigonally-disposed carbohydrate residues is presented as a prelude to attaining chiral discrimination in the complexation of (R)- and (S)-α-phenylethylammonium perchlorate.",

author = "Andrews, {David G.} and Ashton, {Peter R.} and Laidler, {Dale A.} and Stoddart, {J. Fraser} and Wolstenholme, {John B.}",

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T1 - The synthesis of a chiral receptor molecule containing three carbohydrate residues within a 20-crown-6 constitution

AU - Andrews, David G.

AU - Ashton, Peter R.

AU - Laidler, Dale A.

AU - Stoddart, J. Fraser

AU - Wolstenholme, John B.

PY - 1979

Y1 - 1979

N2 - The rationale behind designing and the approach to synthesising chiral crown ethers incorporating three trigonally-disposed carbohydrate residues is presented as a prelude to attaining chiral discrimination in the complexation of (R)- and (S)-α-phenylethylammonium perchlorate.

AB - The rationale behind designing and the approach to synthesising chiral crown ethers incorporating three trigonally-disposed carbohydrate residues is presented as a prelude to attaining chiral discrimination in the complexation of (R)- and (S)-α-phenylethylammonium perchlorate.

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U2 - 10.1016/S0040-4039(01)86369-3

DO - 10.1016/S0040-4039(01)86369-3

M3 - Article

AN - SCOPUS:0000840456

SN - 0040-4039

VL - 20

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EP - 2632

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 28

ER -

The synthesis of a chiral receptor molecule containing three carbohydrate residues within a 20-crown-6 constitution

Abstract

ASJC Scopus subject areas

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