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学科主题: 氟化学
题名: Diastereoselectivity-switchable and regiospecific hetero Diels-Alder reaction of N-sulfinylper(poly)fluoroalkanesulfinamides with dienes reaction; diene
其他题名: 立体选择性可变和区域选择性的N-亚硫酰基全(多)氟烷基亚磺酰胺与共轭二烯的杂Diels-Alder反应
作者: Wang XJ(王小进) ; Liu JT(刘金涛)
通讯作者: 刘金涛
刊名: Tetrahedron
发表日期: 2005-01-01
卷: 61, 期:29, 页:6982-6987
收录类别: SCI
部门归属: 上海有机化学研究所元素有机化学研究室
英文摘要: N-Sulfinylper(poly)fluoroalkanesulfinamides reacted readily with dienes in methylene chloride at -78 degrees C to give the corresponding cycloadducts with complete regioselectivities and good diastereoselectivities. The diastereoselectivity of the reaction was switchable to the opposite under the catalysis of Lewis acids such as TiCl4 and SnCl4. (c) 2005 Elsevier Ltd. All rights reserved.
语种: 英语
相关网址: 查看原文
内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/23326
Appears in Collections:中科院有机氟化学重点实验室_期刊论文

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Recommended Citation:
Wang XJ,Liu JT. Diastereoselectivity-switchable and regiospecific hetero Diels-Alder reaction of N-sulfinylper(poly)fluoroalkanesulfinamides with dienes reaction; diene[J]. Tetrahedron,2005,61(29):6982-6987.
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