| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278710 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
The mode of reaction of the 1,2,3,4,5,6,7-heptamethoxycarbonylcycloheptatriene with primary amines depends on the reaction conditions and leads to selective formation of N-substituted (heptamethoxycarbonyl)nortrop-2-enes and/or 3-vinylpyridin-2-ones bearing six ester groups. The influence of the solvent on the selectivity of the formation of nortropenes and pyridinones was studied.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yury V. Tomilov, Dmitry N. Platonov, Galina P. Okonnishnikova,