| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5281096 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
Ethyl 6-methyl-pyrimidine-2-one-5-carboxylates react with C-nucleophiles in a diversity oriented synthetic sequence to afford C4 substituted congeners of medicinally potent Biginelli dihydropyrimidinones, in a highly regioselective manner.
Graphical abstractEthyl 6-methyl-pyrimidine-2-one-5-carboxylates react with C-nucleophiles in a diversity oriented synthetic sequence to afford C4 substituted congeners of medicinally potent Biginelli dihydropyrimidinones, in a highly regioselective manner.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kamaljit Singh, Divya Arora, Sukhdeep Singh,