Davenport Laboratories, Department of Chemistry, University of Toronto, 80 St George Street, Toronto, Ontario M5S 3H6, Canada.
Nat Chem. 2015 Nov;7(11):863-70. doi: 10.1038/nchem.2372.
The Catellani reaction--a palladium-catalysed C-H functionalization reaction mediated by norbornene--was first reported in 1997. The capacity to functionalize both the ortho and ipso positions of aryl halides in a single transformation held great appeal. We reported an annulative Catellani reaction in 2000. Since then, our two groups have explored the synthetic utility of this reaction and dramatic progress has been made by a number of groups in the past five years. Whereas the original Catellani reaction uses Pd(0) catalysts, recent studies have shown that Pd(II) catalysts can be used in combination with norbornene to effect (1) direct 2-alkylation of indoles and pyrroles and (2) selective meta-C-H functionalization of arenes bearing commonly used ortho-directing groups, thereby opening new avenues for future research. We describe the most recent developments concerning the Pd-catalysed norbornene-mediated C-H functionalization of arenes, including applications in natural products synthesis. We outline challenges and future opportunities.
卡泰兰尼反应——一种由降冰片烯介导的钯催化 C-H 功能化反应——于 1997 年首次报道。该反应能够在单个转化中官能化芳基卤化物的邻位和对位,这具有很大的吸引力。我们在 2000 年报道了一个环加成卡泰兰尼反应。自那时以来,我们两个小组已经探索了该反应的合成实用性,并且在过去五年中,许多小组在这方面取得了显著进展。虽然最初的卡泰兰尼反应使用 Pd(0)催化剂,但最近的研究表明,Pd(II)催化剂可以与降冰片烯结合使用,从而实现(1)吲哚和吡咯的直接 2-烷基化,以及(2)具有常用邻位导向基团的芳烃的选择性间位 C-H 功能化,从而为未来的研究开辟了新途径。我们描述了有关钯催化的降冰片烯介导的芳烃 C-H 功能化的最新进展,包括在天然产物合成中的应用。我们概述了挑战和未来的机会。