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Rh(III)-催化的(杂)芳基与烯丙醇的脱氢烷基化反应,可实现与茚的羟醛缩合。

Rh(III)-catalyzed dehydrogenative alkylation of (hetero)arenes with allylic alcohols, allowing aldol condensation to indenes.

机构信息

Universität Münster Organisch-Chemisches Institut, Corrensstrasse 40, 48149 Münster, Germany.

出版信息

Chem Commun (Camb). 2013 Jul 25;49(58):6489-91. doi: 10.1039/c3cc43903h. Epub 2013 Jun 14.

DOI:10.1039/c3cc43903h
PMID:23765402
Abstract

Efficient Rh(III)-catalyzed C-H activation of different classes of (hetero)arenes such as 2-phenylpyridine, indoles, aryl ketones and acetanilide and their dehydrogenative cross-coupling with allylic alcohols are described. Several important skeletons such as β-aryl aldehydes and ketones, 2-acetylindenes, 3,4-dihydro-1H-quinolin-2-one and quinoline could be produced using this protocol.

摘要

描述了高效的 Rh(III)-催化不同类型(杂)芳基 C-H 活化,如 2-苯基吡啶、吲哚、芳基酮和乙酰苯胺,以及它们与烯丙醇的脱氢交叉偶联。该方法可用于生成多种重要骨架,如β-芳基醛和酮、2-乙酰基茚、3,4-二氢-1H-喹啉-2-酮和喹啉。

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