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首页> 外文期刊>Tetrahedron >Preparation of perfluorocyclopentenylmetal species and their cross-coupling reaction with electrophiles - Remarkable accesses to versatile perfluorocyclopentene derivatives
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Preparation of perfluorocyclopentenylmetal species and their cross-coupling reaction with electrophiles - Remarkable accesses to versatile perfluorocyclopentene derivatives

机译:全氟环戊烯基金属物质的制备及其与亲电试剂的交叉偶联反应-大量获得通用全氟环戊烯衍生物的途径

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On treating perfluorocyclopentene with bis(tributylstannyl)cyanocuprate in THF at -78 degrees C for 1 h, perfluorocyclopentenylstannane was obtained in good yield. The reaction of the fluorinated vinylstannane with n-BuLi in THF at -78 degrees C for 1 h, followed by addition of carbonyl compounds, gave the corresponding allyl alcohols in good yields. On the other hand, Pd(0)-catalyzed cross-coupling reaction of perfluorocyclopenterylstannane with benzyl chloroformate in THF at reflux temperature for 2 h proceeded smoothly to form the decarbonated coupling product in high yield. (c) 2008 Elsevier Ltd. All rights reserved.
机译:在-78℃下用双(三丁基锡烷基)氰基丙二酸酯在THF中处理全氟环戊烯1小时,以良好的产率获得了全氟环戊烯锡烷。氟化乙烯基锡烷与正丁基锂在-78℃下于THF中反应1小时,然后添加羰基化合物,得到相应的烯丙醇,收率很高。另一方面,Pd(0)催化全氟环戊基锡烷与氯甲酸苄酯在THF中回流温度下2h的交叉偶联反应顺利进行,以高收率形成脱碳偶联产物。 (c)2008 Elsevier Ltd.保留所有权利。

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