Supramolecular macrocycles self-assembled by phenanthroline-Cu(I) and sugar-boronic acid interactions

Masashi Yamamoto; Masayuki Takeuchi; Seiji Shinkai

doi:10.1016/S0040-4039(00)00370-1

Supramolecular macrocycles self-assembled by phenanthroline-Cu(I) and sugar-boronic acid interactions

Masashi Yamamoto, Masayuki Takeuchi, Seiji Shinkai

Institute for Advanced Study

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

7 Citations (Scopus)

Abstract

Two kinds of ligand which have two phenanthroline groups linked by a C₂-symmetrical chiral tetrol were synthesized by a boronic acid-diol interaction. It was shown that these ligands form unique dinuclear chiral macrocycles by a Cu(I)-phenanthroline interaction. The results indicate that a novel supramolecular system can be exploited by combination of the Cu(I)- phenanthroline interaction with the boronic acid-diol interaction.

Original language	English
Pages (from-to)	3137-3140
Number of pages	4
Journal	Tetrahedron Letters
Volume	41
Issue number	17
DOIs	https://doi.org/10.1016/S0040-4039(00)00370-1
Publication status	Published - Apr 22 2000

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(00)00370-1

Fingerprint Dive into the research topics of 'Supramolecular macrocycles self-assembled by phenanthroline-Cu(I) and sugar-boronic acid interactions'. Together they form a unique fingerprint.

Cite this

@article{b51af9c524f6492eb223cc5f64f2d77a,

title = "Supramolecular macrocycles self-assembled by phenanthroline-Cu(I) and sugar-boronic acid interactions",

abstract = "Two kinds of ligand which have two phenanthroline groups linked by a C2-symmetrical chiral tetrol were synthesized by a boronic acid-diol interaction. It was shown that these ligands form unique dinuclear chiral macrocycles by a Cu(I)-phenanthroline interaction. The results indicate that a novel supramolecular system can be exploited by combination of the Cu(I)- phenanthroline interaction with the boronic acid-diol interaction.",

author = "Masashi Yamamoto and Masayuki Takeuchi and Seiji Shinkai",

year = "2000",

month = apr,

day = "22",

doi = "10.1016/S0040-4039(00)00370-1",

language = "English",

volume = "41",

pages = "3137--3140",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "17",

}

TY - JOUR

T1 - Supramolecular macrocycles self-assembled by phenanthroline-Cu(I) and sugar-boronic acid interactions

AU - Yamamoto, Masashi

AU - Takeuchi, Masayuki

AU - Shinkai, Seiji

PY - 2000/4/22

Y1 - 2000/4/22

N2 - Two kinds of ligand which have two phenanthroline groups linked by a C2-symmetrical chiral tetrol were synthesized by a boronic acid-diol interaction. It was shown that these ligands form unique dinuclear chiral macrocycles by a Cu(I)-phenanthroline interaction. The results indicate that a novel supramolecular system can be exploited by combination of the Cu(I)- phenanthroline interaction with the boronic acid-diol interaction.

AB - Two kinds of ligand which have two phenanthroline groups linked by a C2-symmetrical chiral tetrol were synthesized by a boronic acid-diol interaction. It was shown that these ligands form unique dinuclear chiral macrocycles by a Cu(I)-phenanthroline interaction. The results indicate that a novel supramolecular system can be exploited by combination of the Cu(I)- phenanthroline interaction with the boronic acid-diol interaction.

UR - http://www.scopus.com/inward/record.url?scp=0034701541&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0034701541&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)00370-1

DO - 10.1016/S0040-4039(00)00370-1

M3 - Article

AN - SCOPUS:0034701541

VL - 41

SP - 3137

EP - 3140

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 17

ER -