环辛四烯
抗芳香性
化学
芳香性
立体化学
组合化学
有机化学
分子
作者
Michael Pittelkow,Thomas Hensel,Nicolaj N. Andersen,Malene Plesner
出处
期刊:Synlett
[Thieme Medical Publishers (Germany)]
日期:2015-12-22
卷期号:27 (04): 498-525
被引量:54
标识
DOI:10.1055/s-0035-1560524
摘要
In this account we give an overview of the synthesis and properties of heterocyclic [8]circulenes. Much of the interest in studying heterocyclic [8]circulenes stems from the planar cyclooctatetraene core often contained in these compounds, which in principle is antiaromatic. We start with a short introduction to the hydrocarbon [n]circulenes and proceed to describe the synthetic chemistry involved in creating tetraoxa[8]circulenes, with particular focus on the acid-mediated oligomerization of benzo- or naphthoquinones, resulting in some simple rules for predicting the outcome of the oligomerization reactions. These rules have guided the synthetic strategies for the preparation of azatrioxa[8]circulenes and diazadioxa[8]circulenes, which will be described in separate sections of this account. More traditional synthetic strategies have been applied in the preparation of octathia[8]circulene, tetrathiatetraselena[8]circulene, and a number of other heterocyclic [8]circulenes, and these synthetic efforts will be highlighted. Finally, a section describing structures that are closely related to the heterocyclic [8]circulenes will be presented, and at the end we will comment on the extensive theoretical work regarding the question of aromaticity/antiaromaticity of the central cyclooctatetraene of heterocyclic[8]circulenes. 1 Introduction 2 Synthesis of [n]circulenes 2.1 [4]Circulene 2.2 [5]Circulene 2.3 [6]Circulene 2.4 [7]Circulene 2.5 [8]Circulene 3 Synthesis of Tetraoxa[8]circulenes: A Historical Perspective 4 Synthesis of Azatrioxa[8]circulenes 5 Synthesis of Diazadioxa[8]circulenes 6 Synthesis of Other Heterocyclic [8]Circulenes 7 Synthesis of Structurally Related Compounds 8 Hetero[8]circulenes and Related Compounds as Tools to Study Aromaticity and Antiaromaticity 9 Conclusion and Outlook
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