1. Front Cover: Asmic Isocyanide‐Nitrile Isomerization‐Alkylations (Eur. J. Org. Chem. 29/2019).
- Author
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Alwedi, Embarek, Lujan‐Montelongo, J. Armando, Cortés‐Mejía, Rodrigo, del Campo, Jorge M., Altundas, Bilal, and Fleming, Fraser F.
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LOW temperatures - Abstract
Highlights from the article: Front Cover: Asmic Isocyanide-Nitrile Isomerization-Alkylations (Eur. J. Org. After Asmic is decorated through alkylations (the gymnast on the left), an isocyanide to nitrile isomerization is triggered by the use of I n i BuLi, expelling a transient carbene which receive a reoriented cyanide to afford a lithiated nitrile, whose alkylation leads to a quaternary nitrile (the gymnast with a winning stance on the right). After Asmic is decorated through alkylations (the gymnast on the left), an isocyanide to nitrile isomerization is triggered by the use of I n i BuLi, expelling a transient carbene which receive a reoriented cyanide to afford a lithiated nitrile, whose alkylation leads to a quaternary nitrile (the gymnast with a winning stance on the right).
- Published
- 2019
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