Synthesis and biological evaluation of novel benzoxazinic analogues of ellipticine
✍ Scribed by Deborah Mousset; Rémi Rabot; Pascal Bouyssou; Gérard Coudert; Isabelle Gillaizeau
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 680 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Original 1,4-benzoxazine analogues of ellipticine were prepared using a general synthetic route that relied on an anionic ring annulation as the key transformation. The interest of this approach lies on the possibility of an easy entrance to a wide range of derivatives from the phenol intermediate. In addition, this synthetic strategy offers a smart access to diverse structurally related heteroaryl annulated carbazole analogues of ellipticine just by replacing the starting heterocyclic core. Antiproliferative activities of newly synthesized derivatives were evaluated toward tumor cell lines.
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.