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本文引用的文献

1
How can theory predict the selectivity of palladium-catalyzed cross-coupling of pristine aromatic molecules?理论如何预测钯催化的未功能化芳香分子交叉偶联的选择性?
Chemistry. 2011 Jun 27;17(27):7623-31. doi: 10.1002/chem.201002724. Epub 2011 May 18.
2
Palladium-catalyzed aryl-aryl bond formation through double C-H activation.通过双C-H活化实现钯催化的芳基-芳基键形成。
Top Curr Chem. 2010;292:165-94.
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Aerobic Oxidative Coupling of o-Xylene: Discovery of 2-Fluoropyridine as a Ligand to Support Selective Pd-Catalyzed C-H Functionalization.邻二甲苯的有氧氧化偶联反应:发现2-氟吡啶作为配体用于支持选择性钯催化的C-H官能团化反应
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Carboxylate-assisted transition-metal-catalyzed C-H bond functionalizations: mechanism and scope.羧酸盐辅助的过渡金属催化的C-H键官能团化:机理与范围
Chem Rev. 2011 Mar 9;111(3):1315-45. doi: 10.1021/cr100412j.
5
Catalytic dehydrogenative cross-coupling: forming carbon-carbon bonds by oxidizing two carbon-hydrogen bonds.催化脱氢交叉偶联:通过氧化两个碳氢键形成碳-碳键。
Chem Rev. 2011 Mar 9;111(3):1215-92. doi: 10.1021/cr100280d.
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Palladium-catalyzed oxidative cross-coupling between pyridine N-oxides and indoles.钯催化吡啶 N-氧化物与吲哚的氧化交叉偶联。
Org Lett. 2011 Apr 1;13(7):1766-9. doi: 10.1021/ol200306y. Epub 2011 Mar 9.
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Controlling site selectivity in Pd-catalyzed oxidative cross-coupling reactions.控制 Pd 催化的氧化交叉偶联反应中的位点选择性。
J Am Chem Soc. 2011 Mar 30;133(12):4455-64. doi: 10.1021/ja1097918. Epub 2011 Mar 7.
8
Bond formations between two nucleophiles: transition metal catalyzed oxidative cross-coupling reactions.两个亲核试剂之间的键形成:过渡金属催化的氧化交叉偶联反应
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9
Allylic C-H acetoxylation with a 4,5-diazafluorenone-ligated palladium catalyst: a ligand-based strategy to achieve aerobic catalytic turnover.钯催化烯丙位 C-H 乙酰化反应:一种基于配体的策略实现有氧催化循环。
J Am Chem Soc. 2010 Nov 3;132(43):15116-9. doi: 10.1021/ja105829t.
10
Arylation of unactivated arenes.芳基化反应。
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使用带有 4,5-二氮菲配体的钯催化剂进行吲哚和苯的区域控制有氧氧化偶联。

Regiocontrolled aerobic oxidative coupling of indoles and benzene using Pd catalysts with 4,5-diazafluorene ligands.

机构信息

Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53706, USA.

出版信息

Chem Commun (Camb). 2011 Oct 7;47(37):10257-9. doi: 10.1039/c1cc13632a. Epub 2011 Aug 22.

DOI:10.1039/c1cc13632a
PMID:21860880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3228523/
Abstract

Palladium-catalyzed aerobic oxidative cross-couplings of indoles and benzene have been achieved by using 4,5-diazafluorene derivatives as ancillary ligands. Proper choice of the neutral and anionic ligands enables control over the reaction regioselectivity.

摘要

钯催化吲哚和苯的有氧氧化交叉偶联反应已通过使用 4,5-二氮杂芴衍生物作为辅助配体来实现。通过选择合适的中性和阴离子配体,可以控制反应的区域选择性。