4-Bromoindole structure
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Common Name | 4-Bromoindole | ||
|---|---|---|---|---|
| CAS Number | 52488-36-5 | Molecular Weight | 196.044 | |
| Density | 1.7±0.1 g/cm3 | Boiling Point | 316.9±15.0 °C at 760 mmHg | |
| Molecular Formula | C8H6BrN | Melting Point | 17 °C | |
| MSDS | Chinese USA | Flash Point | 145.5±20.4 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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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 ... |
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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... |
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Optically active total synthesis of clavicipitic acid. Yokoyama Y, et al.
J. Org. Chem. 60(6) , 1486-1487, (1995)
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Metal-halogen exchange of bromoindoles. A route to substituted indoles. Moyer MP, et al.
J. Org. Chem. 51(26) , 5106-5110, (1986)
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