Front Cover Picture: Redox-Neutral Arylations of Vinyl Cation Intermediates (Adv. Synth. Catal. 1/2017)
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- 作者：Daniel Kaiser ; Luis F. Veiros and Nuno Maulide
- 刊名：Advanced Synthesis & Catalysis
- 出版年：2017
- 出版时间：January 4, 2017
- 年：2017
- 卷：359
- 期：1
- 页码：1
- 全文大小：422K
- ISSN：1615-4169
文摘
The front cover image, provided by Giovanni Di Mauro, Daniel Kaiser and Nuno Maulide, illustrates the conversion of vinyl cations, as high-energy intermediates, into systems prone to charge-accelerated Claisen-type [3,3]-sigmatropic rearrangements. Starting from simple precursors, vinyl cation formation enables a rapid increase of molecular complexity, affording α-arylated carbonyl compounds that can be easily elaborated into drug-like scaffolds. The setting to this cascade of reactions is provided by the famous (and beautiful) Karlskirche in Vienna (Foto: G. Kücükkaplan). Further details can be found in the full paper on page 64–77 (D. Kaiser, L. F. Veiros, N. Maulide, Adv. Synth. Catal. 2017, 359, 64–77; DOI: org/10.1002/adsc.201600860" rel="references:https://doi.org/10.1002/adsc.201600860">10.1002/adsc.201600860)