Bis-calix[4]arenes with imine linkages: Synthesis and binding study of thiopheno bis-calix[4]arene with viologens

Gil Tae Hwang; Byeang Hyean Kim

doi:10.1016/S0040-4039(00)00972-2

Bis-calix[4]arenes with imine linkages: Synthesis and binding study of thiopheno bis-calix[4]arene with viologens

Gil Tae Hwang
, Byeang Hyean Kim

Ctr. Biofunctional Molecules

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

27 Scopus citations

Abstract

We have developed an efficient synthetic pathway for various bis- calix[4]arenes with imine linkages by using a simple condensation procedure and carried out the binding study of thiopheno bis-calix[4]arene with biologically interesting viologen guests. (C) 2000 Elsevier Science Ltd.

Original language	English
Pages (from-to)	5917-5921
Number of pages	5
Journal	Tetrahedron Letters
Volume	41
Issue number	31
DOIs	https://doi.org/10.1016/S0040-4039(00)00972-2
State	Published - 29 Jul 2000

Keywords

Calixarenes
Imines
Macrocycles
Molecular recognition

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10.1016/S0040-4039(00)00972-2

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title = "Bis-calix[4]arenes with imine linkages: Synthesis and binding study of thiopheno bis-calix[4]arene with viologens",

abstract = "We have developed an efficient synthetic pathway for various bis- calix[4]arenes with imine linkages by using a simple condensation procedure and carried out the binding study of thiopheno bis-calix[4]arene with biologically interesting viologen guests. (C) 2000 Elsevier Science Ltd.",

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T2 - Synthesis and binding study of thiopheno bis-calix[4]arene with viologens

AU - Hwang, Gil Tae

AU - Kim, Byeang Hyean

PY - 2000/7/29

Y1 - 2000/7/29

N2 - We have developed an efficient synthetic pathway for various bis- calix[4]arenes with imine linkages by using a simple condensation procedure and carried out the binding study of thiopheno bis-calix[4]arene with biologically interesting viologen guests. (C) 2000 Elsevier Science Ltd.

AB - We have developed an efficient synthetic pathway for various bis- calix[4]arenes with imine linkages by using a simple condensation procedure and carried out the binding study of thiopheno bis-calix[4]arene with biologically interesting viologen guests. (C) 2000 Elsevier Science Ltd.

KW - Calixarenes

KW - Imines

KW - Macrocycles

KW - Molecular recognition

UR - https://www.scopus.com/pages/publications/0001737225

U2 - 10.1016/S0040-4039(00)00972-2

DO - 10.1016/S0040-4039(00)00972-2

M3 - Article

AN - SCOPUS:0001737225

SN - 0040-4039

VL - 41

SP - 5917

EP - 5921

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 31

ER -

Bis-calix[4]arenes with imine linkages: Synthesis and binding study of thiopheno bis-calix[4]arene with viologens

Abstract

Keywords

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