Use of ionic liquid for greener glycosidation

Kazunobu Toshima; Kaname Sasaki; Chigusa Yamada

Use of ionic liquid for greener glycosidation

Kazunobu Toshima, Kaname Sasaki, Chigusa Yamada

応用化学科

研究成果: Paper › 査読

抄録

We developed several environmentally benign and stereocontrolled glycosidations using reusable and designable ionic liquids as new reaction media. Several O- and C-glycosides were effectively obtained by theses glycosidation reactions. Therefore, the greener chemical glycosidations including the simple and convenient protocol, and the high chemical yield and stereoselectivity will be very useful for the establishment of Green Carbohydrate Chemistry as a majour branch of Green Chemistry.

本文言語	English
ページ	4172-4173
ページ数	2
出版ステータス	Published - 2006 12月 1
イベント	55th Society of Polymer Science Japan Symposium on Macromolecules - Toyama, Japan 継続期間: 2006 9月 20 → 2006 9月 22

Other

Other	55th Society of Polymer Science Japan Symposium on Macromolecules
国/地域	Japan
City	Toyama
Period	06/9/20 → 06/9/22

ASJC Scopus subject areas

工学（全般）

他のファイルとリンク

引用スタイル

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abstract = "We developed several environmentally benign and stereocontrolled glycosidations using reusable and designable ionic liquids as new reaction media. Several O- and C-glycosides were effectively obtained by theses glycosidation reactions. Therefore, the greener chemical glycosidations including the simple and convenient protocol, and the high chemical yield and stereoselectivity will be very useful for the establishment of Green Carbohydrate Chemistry as a majour branch of Green Chemistry.",

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AU - Toshima, Kazunobu

AU - Sasaki, Kaname

AU - Yamada, Chigusa

PY - 2006/12/1

Y1 - 2006/12/1

N2 - We developed several environmentally benign and stereocontrolled glycosidations using reusable and designable ionic liquids as new reaction media. Several O- and C-glycosides were effectively obtained by theses glycosidation reactions. Therefore, the greener chemical glycosidations including the simple and convenient protocol, and the high chemical yield and stereoselectivity will be very useful for the establishment of Green Carbohydrate Chemistry as a majour branch of Green Chemistry.

AB - We developed several environmentally benign and stereocontrolled glycosidations using reusable and designable ionic liquids as new reaction media. Several O- and C-glycosides were effectively obtained by theses glycosidation reactions. Therefore, the greener chemical glycosidations including the simple and convenient protocol, and the high chemical yield and stereoselectivity will be very useful for the establishment of Green Carbohydrate Chemistry as a majour branch of Green Chemistry.

KW - Carbohydrate

KW - Glycosidation

KW - Green carbohydrate chemistry

KW - Green chemistry

KW - Ionic liquid

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T2 - 55th Society of Polymer Science Japan Symposium on Macromolecules

Y2 - 20 September 2006 through 22 September 2006

ER -

Use of ionic liquid for greener glycosidation

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Other

ASJC Scopus subject areas

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