Calix[4]arene-based ditopic receptor for dicarboxylates

Takeharu Haino; Masaki Nakamura; Nobuki Kato; Miki Hiraoka; Yoshimasa Fukazawa

doi:10.1016/j.tetlet.2004.01.118

Calix[4]arene-based ditopic receptor for dicarboxylates

Takeharu Haino, Masaki Nakamura, Nobuki Kato, Miki Hiraoka, Yoshimasa Fukazawa

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

35 Citations (Scopus)

Abstract

Shape-selective recognition for the dicarboxylates in DMSO can be attained by a new calix[4]arene-based receptor 1 having two urea groups. Biologically active chorismate selectively bound in 1 over its dehydrated derivative. Molecular mechanics calculations gave a plausible explanation for the selective binding.

Original language	English
Pages (from-to)	2281-2284
Number of pages	4
Journal	Tetrahedron Letters
Volume	45
Issue number	11
DOIs	https://doi.org/10.1016/j.tetlet.2004.01.118
Publication status	Published - 2004 Feb 8
Externally published	Yes

Keywords

Calix[4]arene
Host-guest chemistry
Hydrogen bonding
Molecular mechanics
Supramolecular chemistry

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2004.01.118

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title = "Calix[4]arene-based ditopic receptor for dicarboxylates",

abstract = "Shape-selective recognition for the dicarboxylates in DMSO can be attained by a new calix[4]arene-based receptor 1 having two urea groups. Biologically active chorismate selectively bound in 1 over its dehydrated derivative. Molecular mechanics calculations gave a plausible explanation for the selective binding.",

keywords = "Calix[4]arene, Host-guest chemistry, Hydrogen bonding, Molecular mechanics, Supramolecular chemistry",

author = "Takeharu Haino and Masaki Nakamura and Nobuki Kato and Miki Hiraoka and Yoshimasa Fukazawa",

year = "2004",

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T1 - Calix[4]arene-based ditopic receptor for dicarboxylates

AU - Haino, Takeharu

AU - Nakamura, Masaki

AU - Kato, Nobuki

AU - Hiraoka, Miki

AU - Fukazawa, Yoshimasa

PY - 2004/2/8

Y1 - 2004/2/8

N2 - Shape-selective recognition for the dicarboxylates in DMSO can be attained by a new calix[4]arene-based receptor 1 having two urea groups. Biologically active chorismate selectively bound in 1 over its dehydrated derivative. Molecular mechanics calculations gave a plausible explanation for the selective binding.

AB - Shape-selective recognition for the dicarboxylates in DMSO can be attained by a new calix[4]arene-based receptor 1 having two urea groups. Biologically active chorismate selectively bound in 1 over its dehydrated derivative. Molecular mechanics calculations gave a plausible explanation for the selective binding.

KW - Calix[4]arene

KW - Host-guest chemistry

KW - Hydrogen bonding

KW - Molecular mechanics

KW - Supramolecular chemistry

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U2 - 10.1016/j.tetlet.2004.01.118

DO - 10.1016/j.tetlet.2004.01.118

M3 - Article

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EP - 2284

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 11

ER -

Calix[4]arene-based ditopic receptor for dicarboxylates

Abstract

Keywords

ASJC Scopus subject areas

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