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Titlebook: Helicene Chemistry; From Synthesis to Ap Chuan-Feng Chen,Yun Shen Book 2017 Springer-Verlag Berlin Heidelberg 2017 Diels-Alder addition.Fri

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hreibung erfolgt auf der Grundlage des Grundvorstellungskonzepts (vom Hofe, 1995), das zunächst eingehend erörtert und vor dem Hintergrund der zuvor dargestellten theoretischen Transferperspektiven diskutiert wird. Im Anschluss werden Grundvorstellungen und Zahlaspekte von Bruchzahlen auf normativer
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Introduction to Helicene Chemistrycussed in detail, and some landmarks such as the first reported helicene, the demonstration of helical structure by X-ray analysis, the first large-scale synthesis by Diels-Alder addition, and the contributions of leading research groups at different times are highlighted. This book is aimed to beco
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Structures and Properties of Helicenes helicenes are a kind of polycyclic aromatic hydrocarbons with helical chirality, they exhibit specific physical properties and optical properties, especially the excellent luminescent properties. For example, some helicenes display high fluorescence quantum yields in both solution and solid states.
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Oxidative Photocyclizationicient way to the synthesis of heterohelicenes including azahelicenes and thiahelicenes. In this chapter, we first introduce the synthesis of various carbohelicenes by different oxidative photocyclization strategy starting from the stilbene precursors. With two aryl groups in the stilbene precursors
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Metal-Mediated Reactionsparation of helicenes due to their high efficiency (usually constructing more than one ring in one step), moderate to high yields, good functional group tolerance, and the ability to prepare longer helicenes. In this chapter, the [2+2+2] cycloisomerization is first introduced, in which the construct
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Other Synthetic Methodstions or cascade radical cyclizations, but the regioselectivity may be a problem for some cases. By oxidative coupling method, BINOL analogues are widely utilized for the preparation of oxahelicenes, while iterative modular synthesis is employed to prepare extended helicene structures and longer hel
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