Palladium-Catalyzed Reactions of Allylic Boronic Esters with Nucleophiles: Novel Umpolung Reactivity

Palladium-Catalyzed Reactions of Allylic Boronic Esters with Nucleophiles: Novel Umpolung Reactivity
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钯催化烯丙基硼酯与亲核试剂的反应:新型 Umpolung 反应性

DOI:
10.1055/s-0034-1380869
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发表时间:
2015
期刊:
影响因子:
2
通讯作者:
Aggarwal V
Aggarwal V
中科院分区:
化学4区
文献类型:
--
作者:
Aggarwal V

文献摘要

相似文献

氧化钯催化的反应条件已被开发,以允许区域选择性和立体选择性的偶联烯丙基硼酸酯与一系列的碳,氧,和氮基亲核试剂。对反应机理的研究表明,关键的金属转移步骤发生在保留立体化学的情况下,因为观察到了整体反转。
Oxidative palladium-catalyzed reaction conditions have been developed to allow for regioselective and stereoselective coupling of allylic boronic esters with a range of carbon-, oxygen-, and nitrogen-based nucleophiles. Studies into the mechanism of the reaction have shown that the key transmetalation step occurs with retention of stereochemistry, since overall inversion is observed.