Abstract
The formation of two hydrogen bonds between an amidopyridine and a carboxylic acid controls the stereochemical outcome and significantly accelerates the rate of the Diels-Alder cycloaddition between a benzoylpyrrole and a maleimide. (C) 2001 Published by Elsevier Science Ltd.
| Original language | English |
|---|---|
| Pages (from-to) | 2377-2380 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 42 |
| Publication status | Published - 18 Mar 2001 |
Keywords
- CYCLOADDITION