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 |
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Pages (from-to) | 2377-2380 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 42 |
Publication status | Published - 18 Mar 2001 |
Keywords
- CYCLOADDITION