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首页> 外文期刊>Angewandte Chemie >Practical One-Pot Preparation of Magnesium Di(hetero)aryl- and Magnesium Dialkenylboronates for Suzuki-Miyaura Cross-Coupling Reactions
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Practical One-Pot Preparation of Magnesium Di(hetero)aryl- and Magnesium Dialkenylboronates for Suzuki-Miyaura Cross-Coupling Reactions

机译:铃木-Miyaura交叉偶联反应的一锅法制备二(杂)芳基镁和二烯基硼酸镁

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摘要

Arylboron derivatives have found broad applications in Suzuki-Miyaura cross-coupling reactions. In particular, various boronic acids, esters, and their derivatives, such as trifluoroborates, MIDA boronates or DAN reagents, have been used very successfully (MIDA = N-methyliminodi-acetic acid, DAN = 2,3-diaminonaphthalene). In general, most arylboronic compounds are prepared via lithium or magnesium organometallic compounds in a two-step process, although direct transition-metal-catalyzed borylations can also be realized. Furthermore, a one-pot preparation of arylboronic esters by using an iodine/magnesium exchange has been reported.
机译:芳基硼衍生物已在Suzuki-Miyaura交叉偶联反应中得到广泛应用。特别地,已经非常成功地使用了各种硼酸,酯及其衍生物,例如三氟硼酸酯,MIDA硼酸酯或DAN试剂(MIDA = N-甲基亚氨基二乙酸,DAN = 2,3-二氨基萘)。通常,大多数芳基硼化合物是通过锂或镁有机金属化合物以两步法制备的,尽管也可以实现直接过渡金属催化的硼化。此外,已经报道了通过使用碘/镁交换一锅制备芳基硼酸酯的方法。

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