Front Cover: Rearrangement Reactions in Aza‐Vinylogous Povarov Products: Metal‐Free Synthesis of C3‐Functionalized Quinolines and Studies on their Synthetic Application (Eur. J. Org. Chem. 38/2019)

The Front Cover shows a rearrangement reaction, which is represented by the final stage in the resolution of the Rubik‐s cube that finally clicks all elements of the puzzle into place. In this particular case, the rearrangement of a 4,4‐disubstituted tetrahydroquinoline into the corresponding aromat...

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Bibliographic Details
Published in:European journal of organic chemistry 2019-10, Vol.2019 (38), p.6422-6422
Main Authors: Clerigué, José, Bianchini, Giulia, Ribelles, Pascual, Tejero, Tomás, Merino, Pedro, Ramos, M. Teresa, Menéndez, J. Carlos
Format: Article
Language:English
Online Access:Get full text
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Summary:The Front Cover shows a rearrangement reaction, which is represented by the final stage in the resolution of the Rubik‐s cube that finally clicks all elements of the puzzle into place. In this particular case, the rearrangement of a 4,4‐disubstituted tetrahydroquinoline into the corresponding aromatic quinoline was achieved, where a functional group was rearranged to C‐3. This transformation took place under thermal conditions or in the presence of DDQ. More information can be found in the Full Paper by P. Merino, J. C. Menéndez et al.
ISSN:1434-193X
1099-0690
DOI:10.1002/ejoc.201901374