4-溴吲哚
4-溴吲哚结构式
|
常用名 | 4-溴吲哚 | 英文名 | 4-Bromoindole |
|---|---|---|---|---|
| CAS号 | 52488-36-5 | 分子量 | 196.044 | |
| 密度 | 1.7±0.1 g/cm3 | 沸点 | 316.9±15.0 °C at 760 mmHg | |
| 分子式 | C8H6BrN | 熔点 | 17 °C | |
| MSDS | 中文版 美版 | 闪点 | 145.5±20.4 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
|
A concise and scalable strategy for the total synthesis of dictyodendrin B based on sequential C-H functionalization.
Angew. Chem. Int. Ed. Engl. 54(18) , 5451-5, (2015) A sequential CH functionalization strategy for the synthesis of the marine alkaloid dictyodendrin B is reported. Our synthesis begins from commercially available 4-bromoindole and involves six direct functionalizations around the heteroarene core as part of ... |
|
|
Applications of vinylogous Mannich reactions. Total syntheses of the Ergot alkaloids rugulovasines A and B and setoclavine.
J. Am. Chem. Soc. 123(25) , 5918-24, (2001) Concise syntheses of the Ergot alkaloids rugulovasine A (3a), rugulovasine B (3b), and setoclavine (2) have been completed by strategies that feature inter- and intramolecular vinylogous Mannich reactions as the key steps. Thus, the first synthesis of 3a,b co... |
|
|
Optically active total synthesis of clavicipitic acid. Yokoyama Y, et al.
J. Org. Chem. 60(6) , 1486-1487, (1995)
|
|
|
Metal-halogen exchange of bromoindoles. A route to substituted indoles. Moyer MP, et al.
J. Org. Chem. 51(26) , 5106-5110, (1986)
|