A convenient synthesis of new sugar amino acid: 3-aminomethyl-3-deoxy-1,2-O-isopropylide-alpha-D-ribo-hexofuranuronic acid

被引：0

作者：

Turks, M ^{[1
]}

Katkevica, D ^{[1
]}

Smits, H ^{[1
]}

Bizdena, E ^{[1
]}

机构：

[1] Riga Tech Univ, Fac Chem Technol, LV-1048 Riga, Latvia

来源：

CHEMISTRY OF NUCLEIC ACID COMPONENTS | 1999年 / 2卷

关键词：

D O I：

暂无

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Efficient synthesis of protected 3-aminomethyl-3-deoxy-1,2-O-isopropylidene-alpha-D-ribo-hexofuranuronic acid 1 has been developed. The key reaction in this route is the creation of new C-C bonds in positions C(3) and C(5), which was achieved by nitromethane addition to carbonyl derivatives of sugar (Henry reaction).

引用

页码：268 / 272

页数：5

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