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通过铱催化的区域选择性笼状硼氢键和碳(sp)-氢键活化实现邻碳硼烷与噻吩的脱氢交叉偶联。

Dehydrogenative cross-coupling of o-carborane with thiophenes via Ir-catalyzed regioselective cage B-H and C(sp)-H activation.

作者信息

Quan Yangjian, Lyu Hairong, Xie Zuowei

机构信息

Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China.

出版信息

Chem Commun (Camb). 2017 Apr 27;53(35):4818-4821. doi: 10.1039/c7cc01485f.

DOI:10.1039/c7cc01485f
PMID:28417119
Abstract

Ir-Catalyzed -COOH directed site-selective B-H/C-H dehydrogenative cross-coupling of o-carborane with thiophenes has been achieved for the first time. Without any pre-functionalization, carboranyl carboxylic acids and thiophenes can serve as suitable coupling partners, resulting in the preparation of 4-thienyl-o-carboranes in a simple one-pot process for potential applications in materials.

摘要

首次实现了铱催化的邻碳硼烷的-COOH导向的位点选择性B-H/C-H脱氢交叉偶联与噻吩的反应。无需任何预官能团化,碳硼烷基羧酸和噻吩可作为合适的偶联伙伴,通过简单的一锅法制备4-噻吩基邻碳硼烷,用于材料的潜在应用。

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