The synthesis of azophenolic crown ethers of Cs symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces

Koichiro Naemura; Sachiko Takeuchi; Masaki Asada; Keiji Hirose; Yoshito Tobe; Takahiro Kaneda; Yoshiteru Sakata

doi:10.1039/C39940000711

The synthesis of azophenolic crown ethers of C_s symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces

Koichiro Naemura^*, Sachiko Takeuchi, Masaki Asada, Keiji Hirose, Yoshito Tobe, Takahiro Kaneda, Yoshiteru Sakata

^*Corresponding author for this work

Department of Applied Chemistry

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

11 Scopus citations

Abstract

Azophenolic crown ethers 9 and 10 of C_s symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues as a steric barrier have been prepared; they bind ethanolamine stereoselectively to one of their diastereotopic faces.

Original language	English
Pages (from-to)	711-712
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	6
DOIs	https://doi.org/10.1039/C39940000711
State	Published - 1 Dec 1994

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Naemura, K., Takeuchi, S., Asada, M., Hirose, K., Tobe, Y., Kaneda, T., & Sakata, Y. (1994). The synthesis of azophenolic crown ethers of C_s symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces. Journal of the Chemical Society, Chemical Communications, (6), 711-712. https://doi.org/10.1039/C39940000711

Naemura, Koichiro ; Takeuchi, Sachiko ; Asada, Masaki ; Hirose, Keiji ; Tobe, Yoshito ; Kaneda, Takahiro ; Sakata, Yoshiteru. / The synthesis of azophenolic crown ethers of C_s symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces. In: Journal of the Chemical Society, Chemical Communications. 1994 ; No. 6. pp. 711-712.

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title = "The synthesis of azophenolic crown ethers of Cs symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces",

abstract = "Azophenolic crown ethers 9 and 10 of Cs symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues as a steric barrier have been prepared; they bind ethanolamine stereoselectively to one of their diastereotopic faces.",

author = "Koichiro Naemura and Sachiko Takeuchi and Masaki Asada and Keiji Hirose and Yoshito Tobe and Takahiro Kaneda and Yoshiteru Sakata",

year = "1994",

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day = "1",

doi = "10.1039/C39940000711",

language = "English",

pages = "711--712",

journal = "Chemical Communications",

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Naemura, K, Takeuchi, S, Asada, M, Hirose, K, Tobe, Y, Kaneda, T & Sakata, Y 1994, 'The synthesis of azophenolic crown ethers of C_s symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces', Journal of the Chemical Society, Chemical Communications, no. 6, pp. 711-712. https://doi.org/10.1039/C39940000711

The synthesis of azophenolic crown ethers of C_s symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces. / Naemura, Koichiro; Takeuchi, Sachiko; Asada, Masaki; Hirose, Keiji; Tobe, Yoshito; Kaneda, Takahiro; Sakata, Yoshiteru.

In: Journal of the Chemical Society, Chemical Communications, No. 6, 01.12.1994, p. 711-712.

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

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T1 - The synthesis of azophenolic crown ethers of Cs symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces

AU - Naemura, Koichiro

AU - Takeuchi, Sachiko

AU - Asada, Masaki

AU - Hirose, Keiji

AU - Tobe, Yoshito

AU - Kaneda, Takahiro

AU - Sakata, Yoshiteru

PY - 1994/12/1

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N2 - Azophenolic crown ethers 9 and 10 of Cs symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues as a steric barrier have been prepared; they bind ethanolamine stereoselectively to one of their diastereotopic faces.

AB - Azophenolic crown ethers 9 and 10 of Cs symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues as a steric barrier have been prepared; they bind ethanolamine stereoselectively to one of their diastereotopic faces.

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JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

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Naemura K, Takeuchi S, Asada M, Hirose K, Tobe Y, Kaneda T et al. The synthesis of azophenolic crown ethers of C_s symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces. Journal of the Chemical Society, Chemical Communications. 1994 Dec 1;(6):711-712. https://doi.org/10.1039/C39940000711

The synthesis of azophenolic crown ethers of Cs symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces

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The synthesis of azophenolic crown ethers of C_s symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces