Convenient Regioselective mono-2-O-Sulfonation of Cyclomaltooctaose
スポンサーリンク
概要
- 論文の詳細を見る
Regioselective mono-2-O-sulfonation of cyclomaltooctaose was conveniently achieved by using the combination of sulfonyl imidazole and molecular sieves in DMF. In this reaction, no 3-O- or 6-O-sulfonation products were produced. The reactions do not require strict anhydrous or basic conditions, or specific sulfonyl groups.
- 社団法人日本農芸化学会の論文
- 1998-06-23
著者
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Hisamatsu Makoto
Faculty of Bioresources, Mie University
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Teranishi K
Department Of Agricultural Chemistry Faculty Of Bioresources Mie University
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Teranishi Katsunori
Faculty Of Bioresources Mie University
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Hisamatsu M
Department Of Agricultural Chemistry Faculty Of Bioresources Mie University
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Hisamatsu Makoto
Faculty Of Bioresources Mie University
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Yamada Tetsuya
Faculty of Bioresources, Mie University
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TANABE Saori
Faculty of Bioresources, Mie University
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Tanabe Saori
Faculty Of Bioresources Mie University
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Yamada Tetsuya
Faculty Of Bioresources Mie University
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Yamada T
National Institute Of Agrobiological Sciences Ministry Of Agriculture Forestry And Fisheries
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Tanabe Saori
Department Of Pediatrics Yamagata Prefectural And Sakata Municipal Hospital Organization
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YAMADA Tetsuya
Faculties of Bioresource, Mie University
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