An efficient chiral stationary phase for high performance liquid chromatographic separation of enantiomeric aliphatic alcohols

Shuichi Ôi; Masayuki Shijo; Junzo Yamashita; Sotaro Miyano

doi:10.1246/cl.1988.1545

An efficient chiral stationary phase for high performance liquid chromatographic separation of enantiomeric aliphatic alcohols

Shuichi Ôi, Masayuki Shijo, Junzo Yamashita, Sotaro Miyano

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

11 Citations (Scopus)

Abstract

(S)-1,1′-Binaphthyl-2,2′-dicarboxylic acid was chemically bonded to an aminopropylsilanized silica through amido linkage to give a chiral stationary phase for HPLC, which efficiently differentiated enantiomeric aliphatic alcohols as 3,5-dinitrophenylcarbamates.

Original language	English
Pages (from-to)	1545-1546
Number of pages	2
Journal	Chemistry Letters
Volume	17
Issue number	9
DOIs	https://doi.org/10.1246/cl.1988.1545
Publication status	Published - 1988 Jan 1
Externally published	Yes

ASJC Scopus subject areas

Chemistry(all)

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title = "An efficient chiral stationary phase for high performance liquid chromatographic separation of enantiomeric aliphatic alcohols",

abstract = "(S)-1,1′-Binaphthyl-2,2′-dicarboxylic acid was chemically bonded to an aminopropylsilanized silica through amido linkage to give a chiral stationary phase for HPLC, which efficiently differentiated enantiomeric aliphatic alcohols as 3,5-dinitrophenylcarbamates.",

author = "Shuichi {\^O}i and Masayuki Shijo and Junzo Yamashita and Sotaro Miyano",

year = "1988",

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doi = "10.1246/cl.1988.1545",

language = "English",

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T1 - An efficient chiral stationary phase for high performance liquid chromatographic separation of enantiomeric aliphatic alcohols

AU - Ôi, Shuichi

AU - Shijo, Masayuki

AU - Yamashita, Junzo

AU - Miyano, Sotaro

PY - 1988/1/1

Y1 - 1988/1/1

N2 - (S)-1,1′-Binaphthyl-2,2′-dicarboxylic acid was chemically bonded to an aminopropylsilanized silica through amido linkage to give a chiral stationary phase for HPLC, which efficiently differentiated enantiomeric aliphatic alcohols as 3,5-dinitrophenylcarbamates.

AB - (S)-1,1′-Binaphthyl-2,2′-dicarboxylic acid was chemically bonded to an aminopropylsilanized silica through amido linkage to give a chiral stationary phase for HPLC, which efficiently differentiated enantiomeric aliphatic alcohols as 3,5-dinitrophenylcarbamates.

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DO - 10.1246/cl.1988.1545

M3 - Article

AN - SCOPUS:84912951833

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JO - Chemistry Letters

JF - Chemistry Letters

SN - 0366-7022

IS - 9

ER -

An efficient chiral stationary phase for high performance liquid chromatographic separation of enantiomeric aliphatic alcohols

Abstract

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