The use of 1-hydrazinodienes in the Diels-Alder reaction is adding a new twist to the well-studied reaction: The cycloaddition product may be driven to rearrange, according to research by Princeton ...
The Diels-Alder reaction is a classic transformation that typically marries a diene (with four π electrons) and an alkene (with two π electrons) to form a six-membered ring—it’s known as a [4+2] ...
The Diels-Alder reaction is the most iconic organic chemistry reaction. Scientists now report on exactly how this chemical reaction, discovered in 1928, occurs. In 1928, chemists Otto Diels and Kurt ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback