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首页> 外文期刊>有機合成化学協会誌 >Cyclization Reactions using Vinyl Sulfides and Vinyl Selenides: Recent Developments towards Organic Synthesis
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Cyclization Reactions using Vinyl Sulfides and Vinyl Selenides: Recent Developments towards Organic Synthesis

机译:使用乙烯基硫化物和乙烯基硒化物的环化反应:有机合成的最新进展

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Cyclization reactions using vinyl sulfides and vinyl selenides have recently attracted much attention. One of the major characteristics of sulfur-and selenium-substituted donor olefins is a large HOMO coefficient on the hetero-atom. Due to such specific character, sulfur and selenium-substituents can be used as selectivity-controlling elements in cyclizations. Novel reactions resulting from a combination with other elements, such as [2+1] cycloadditions of 1-seleno-2-silylethenes, are also described. After the cyclization steps, sulfur and selenium are useful for various functional group transformations. In this review, [2+1], [2+2], [3+2], and [4+2] cycloaddition reactions employing vinyl sulfides and selenides in organic synthesis are outlined.
机译:使用乙烯基硫化物和乙烯基硒化物的环化反应最近引起了很多关注。硫和硒取代的供体烯烃的主要特征之一是杂原子上的HOMO系数大。由于这种特殊的特性,硫和硒取代基可用作环化反应中的选择性控制元素。还描述了由与其他元素(例如1-硒代-2-甲硅烷基的[2 + 1]环加成)结合产生的新反应。在环化步骤之后,硫和硒可用于各种官能团转化。在这篇综述中,概述了在有机合成中使用乙烯基硫化物和硒化物的[2 + 1],[2 + 2],[3 + 2]和[4 + 2]环加成反应。

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