A novel synthesis of s-triazoloazines fused at the N2C3 bond of the triazole ring
✍ Scribed by S. Polanc; B. Verček; B. Stanovnik; M. Tišler
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 156 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The reaction of the dilithio derivative of dimethyl cis-4-cyclohexen-1,2-dicarboxylate with 3substituted propiolic acid phenyl esters proceeds via an unusual mechanistic path to generate fused bicyclic 2cyclopentenones in a single step. The first total synthesis of a member of the gingkolide family
Dioxadithiaporphycenes 5 and 5% were synthesized by using the Suzuki cross-coupling and McMurry coupling reactions as the key steps. This approach provided an access to the first dioxadithiaporphycene derivative 15 with a benzene ring fused onto the double bond.