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使用烯烃作为导向基团和反应部分,对联苯的空间位阻较大的 C-C 键进行区域选择性活化。

Regioselective Activation of a Sterically More Hindered C-C Bond of Biphenylenes Using an Alkene as Both a Directing Group and a Reaction Moiety.

机构信息

Department of Chemistry and Biochemistry, School of Advanced Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku, Tokyo, 169-8555, Japan.

Global Center for Science and Engineering, School of Advanced Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku, Tokyo, 169-8555, Japan.

出版信息

Chemistry. 2018 Oct 12;24(57):15173-15177. doi: 10.1002/chem.201804044. Epub 2018 Oct 4.

DOI:10.1002/chem.201804044
PMID:30285307
Abstract

The Rh-catalyzed intramolecular reaction of 1-(2-vinylaryl)-substituted biphenylenes was used to construct a dihydrobenzo[b]fluoranthene skeleton. This transformation was achieved by regioselective C-C bond cleavage of a sterically more hindered biphenylene site by using alkene as both a directing group and a reaction moiety. Furthermore, we measured and analyzed the photophysical properties of the new multicyclic fused compounds.

摘要

铑催化的 1-(2-乙烯基芳基)取代联苯的分子内反应被用于构建二氢苯并[b]荧蒽骨架。这种转化是通过烯烃作为导向基团和反应部分,在空间位阻较大的联苯位置进行区域选择性 C-C 键断裂来实现的。此外,我们还测量和分析了新的多环稠合化合物的光物理性质。

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