2,2′-Biindolyl revisited. Synthesis and reactions
✍ Scribed by Jan Bergman; Eva Koch; Benjamin Pelcman
- Book ID
- 103396942
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 620 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
2,Y-biindolyl (9) has been transformed into indolo[3,2-a]carbazoles 16a-b by means of formal [4 + 2] eycloadditions with co-formation of the Michael adducts 17a-b. The parent indolo[3,2-a]carbazole ( 6) has been prepared in one step from 9 in excellent yield. Several 3-substituted 2,3'-biindolyls ha
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