(4+3) cycloaddition reactions of nitrogen-stabilized oxyallyl cations.

(4+3) cycloaddition reactions of nitrogen-stabilized oxyallyl cations.
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DOI:
10.1002/chem.201100260
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发表时间:
2011-03-28
影响因子:
4.3
通讯作者:
Hsung, Richard P.
Hsung, Richard P.
中科院分区:
化学2区
文献类型:
--
作者:
Lohse, Andrew G.;Hsung, Richard P.

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杂原子取代氧烯丙基阳离子在(4 + 3)环加成中的应用对环加成化学的发展产生了巨大的影响。氧、硫和卤素取代基对氧烯丙基阳离子反应性的影响已经得到了广泛的研究。最近,氮稳定氧烯丙基阳离子的使用在(4 + 3)环加成领域得到了突出的应用。下面的文章将提供利用氮稳定氧烯丙基阳离子这一概念的概述。
The use of heteroatom-substituted oxyallyl cations in (4 + 3) cycloadditions has had a tremendous impact on the development of cycloaddition chemistry. Extensive efforts have been exerted toward investigating the effect of oxygen-, sulfur-, and halogen-substituents on the reactivity of oxyallyl cations. Most recently, the use of nitrogen-stabilized oxyallyl cations has gained prominence in the area of (4 + 3) cycloadditions. The following article will provide an overview of this concept utilizing nitrogen-stabilized oxyallyl cations.
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