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

被引：39

作者：

Hasegawa, T

Umeda, M

Numata, M

Fujisawa, T

Haraguchi, S

Sakurai, K

Shinkai, S

机构：

[1] Kyushu Univ, Grad Sch Engn, Dept Chem, Fukuoka 8128581, Japan

[2] Univ Kitakyushu, Fac Environm Engn, Dept Chem Proc & Environm, Wakamatsu Ku, Kitakyushu, Fukuoka 8080135, Japan

来源：

CHEMISTRY LETTERS | 2006年 / 35卷 / 01期

关键词：

D O I：

10.1246/cl.2006.82

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

beta-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.

引用

页码：82 / 83

页数：2

共 2 条

[1] 'Click chemistry' on polysaccharides:: a convenient, general, and monitorable approach to develop (1→3)-β-D-glucans with various functional appendages
Hasegawa, T
Umeda, M
Numata, M
Li, C
Bae, AH
Fujisawa, T
Haraguchi, S
Sakurai, K
Shinkai, S
CARBOHYDRATE RESEARCH, 2006, 341 (01) : 35 - 40
[2] Click chemistry approach for the regioselective synthesis of iso-indoline-1,3-dione-linked 1,4 and 1,5 coumarinyl 1,2,3-triazoles and their photophysical properties
Anand, Ashish
Kulkarni, Manohar V.
SYNTHETIC COMMUNICATIONS, 2017, 47 (07) : 722 - 733

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