Click chemistry on curdlan: A regioselective and quantitative approach to develop artificial β-1,3-glucans with various functional appendages

Teruaki Hasegawa; Mariko Umeda; Munenori Numata; Tomohisa Fujisawa; Shuichi Haraguchi; Kazuo Sakurai; Seiji Shinkai

doi:10.1246/cl.2006.82

Click chemistry on curdlan: A regioselective and quantitative approach to develop artificial β-1,3-glucans with various functional appendages

Teruaki Hasegawa, Mariko Umeda, Munenori Numata, Tomohisa Fujisawa, Shuichi Haraguchi, Kazuo Sakurai, Seiji Shinkai

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

45 Citations (Scopus)

Abstract

β-1,3-Glucans having various functional appendages (lactoside, ferrocene, pyrene, etc.) can be prepared in an convenient, quantitative, and regioselective manner through chemo-selective [3 + 2]-cycloadditions between 6-azido-6-deoxy-curdlan and various functional modules with a terminal alkyne.

Original language	English
Pages (from-to)	82-83
Number of pages	2
Journal	Chemistry Letters
Volume	35
Issue number	1
DOIs	https://doi.org/10.1246/cl.2006.82
Publication status	Published - Jan 5 2006
Externally published	Yes

All Science Journal Classification (ASJC) codes

Chemistry(all)

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10.1246/cl.2006.82

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AU - Umeda, Mariko

AU - Numata, Munenori

AU - Fujisawa, Tomohisa

AU - Haraguchi, Shuichi

AU - Sakurai, Kazuo

AU - Shinkai, Seiji

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AB - β-1,3-Glucans having various functional appendages (lactoside, ferrocene, pyrene, etc.) can be prepared in an convenient, quantitative, and regioselective manner through chemo-selective [3 + 2]-cycloadditions between 6-azido-6-deoxy-curdlan and various functional modules with a terminal alkyne.

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Click chemistry on curdlan: A regioselective and quantitative approach to develop artificial β-1,3-glucans with various functional appendages

Abstract

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