The enantioselective Diels–Alder reaction stands as a cornerstone of modern synthetic chemistry, enabling the rapid construction of six-membered rings with controlled stereochemistry. By uniting a ...

The Diels–Alder cycloaddition remains one of the most versatile tools for the construction of six-membered rings, enabling rapid build-up of molecular complexity through the union of a conjugated ...

(Phys.org)—The Diels-Alder reaction is a mainstay in organic chemistry. The reaction traditionally involves a diene and a dienophile. The diene has four carbons that are sp 2 hybridized to form pi ...

First reported in 1928 by Otto Diels and Kurt Alder, the Diels-Alder reaction is one of the most relevant transformations in organic chemistry. Its capacity to generate six-membered rings enables the ...