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学科主题: 生命有机化学
题名: An Efficient Route toward 2-Amino-beta-D-galacto- and -glucopyranosides via Stereoselective Michael-Type Addition of 2-Nitroglycals
其他题名: 通过对2-硝基糖烯的立体选择性麦克尔加成高效合成2-氨基-beta-D-半乳糖和葡萄糖苷的方法
作者: Xue WH(薛伟华) ; Sun JS(孙建松) ; Yu B(俞飚)
通讯作者: 俞飚
刊名: J. Org. Chem.
发表日期: 2009
卷: 74, 期:14, 页:5079-5082
收录类别: SCI
部门归属: 上海有机所
英文摘要: Under the catalysis of DMAP or PPY in CH2Cl2, the Michael-type addition of nucleophiles to 2-nitrogalactal or 2-nitroglucal leads in excellent yields and stereoselectivity to the corresponding beta-galacto- or -glucopyranosides, which are ready precursors to the biologically significant beta-D-galactosamine and -glucosamine units.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000268139700023
Citation statistics:
内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/19097
Appears in Collections:生命有机化学国家重点实验室_期刊论文

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Recommended Citation:
Xue WH,Sun JS,Yu B. An Efficient Route toward 2-Amino-beta-D-galacto- and -glucopyranosides via Stereoselective Michael-Type Addition of 2-Nitroglycals[J]. J. Org. Chem.,2009,74(14):5079-5082.
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