Abstract
Triazinane diones, readily generated by a recently reported multicomponent reaction, can be easily
alkylated with various alkyl halides, allowing a wide variety of complexity-generating secondary
reactions. Because of the high variability of the initial multicomponent reactions and the multiple
possibilities for participation of substituents in the secondary reactions, a highly diverse set of complex
products was obtained in short and efficient reaction sequences.
| Original language | Undefined/Unknown |
|---|---|
| Pages (from-to) | 3158-3165 |
| Number of pages | 8 |
| Journal | Organic & Biomolecular Chemistry |
| Volume | 6 |
| Publication status | Published - 2008 |