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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Lithium trihydroxy/triisopropoxy-2-pyridylborate salts (LTBS): synthesis, isolation, and use in modified Suzuki-Miyaura cross-coupling reactions
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Lithium trihydroxy/triisopropoxy-2-pyridylborate salts (LTBS): synthesis, isolation, and use in modified Suzuki-Miyaura cross-coupling reactions

机译:三羟基/三异丙氧基-2-吡啶基硼酸锂盐(LTBS):合成,分离和用于改进的Suzuki-Miyaura交叉偶联反应

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摘要

We describe herein shelf-stable, isolable, and characterizable pyridyl lithium trihydroxy and triisoprop-oxy 2-borate salts (LTBS) for use in modified Suzuki-Miyaura cross-coupling reactions that can be produced in quantities greater than one hundred grams. Pyridyl LTBS provide a viable cross-coupling alternative to unstable 2-pyridylboronic acids, boronates, and trifluoroborate salt derivatives. We also demonstrate the synthesis and cross-coupling of shelf-stable LTBS reagents of other sp~2-hybridized nitrogen-containing heterocycles including thiazole, pyrazine, quinoline, and isoquinoline heterocycles.
机译:我们在本文中描述了可用于大于100克的改性Suzuki-Miyaura交叉偶联反应中使用的货架稳定,可分离和可表征的吡啶基三羟基锂和三异丙氧基2-硼酸盐(LTBS)。吡啶基LTBS为不稳定的2-吡啶基硼酸,硼酸盐和三氟硼酸盐衍生物提供了可行的交叉偶联选择。我们还证明了其他sp〜2杂化的含氮杂环(包括噻唑,吡嗪,喹啉和异喹啉杂环)的货架稳定LTBS试剂的合成和交叉偶联。

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