A novel palladium-catalyzed synthesis of β-carbolines: application in total synthesis of naturally occurring alkaloids
✍ Scribed by Shubhada W Dantale; Björn C.G Söderberg
- Book ID
- 104205475
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 216 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
Two naturally occurring b-carbolines, 6-methoxy-2-methyl-1,2,3,4-tetrahydro-b-carboline and bauerine A, have been prepared using a Stille-type coupling, followed by a palladium-phosphine catalyzed N-heteroannulation as the key steps.
📜 SIMILAR VOLUMES
The first total synthesis of the new type of cytocydal Pcarholine alkaloid oxopropaline G was achieved in 12 steps.
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract The first total synthesis of the β‐carboline alkaloids arenarine A **(1)** and arenarine B **(2)** is described. Methanolysis of the α‐bromoketone **9** gives **1** in good yield. Alternatively **1** can be obtained from the diazoketone **11** with boron trifluoride/methanol in poor yie