| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5266306 | Tetrahedron Letters | 2012 | 5 Pages | 
Abstract
												We present an efficient method for the selective bromination of N-alkylcarbazoles using N-bromosuccinimide (NBS) in THF. Four brominated N-alkylcarbazoles including 3-bromo-, 3,6-dibromo-, 1,3,6-tribromo- and 1,3,6,8-tetrabromo-carbazoles were prepared and identified by 1H NMR spectroscopy. Subsequent cross-coupling of these carbazoles with benzo[b]thien-2-ylboronic acid gave the corresponding benzo[b]thien-2-yl functionalized carbazoles in good yields.
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											Authors
												Sukrawee Pansay, Narid Prachumrak, Siriporn Jungsuttiwong, Tinnagon Keawin, Taweesak Sudyoadsuk, Vinich Promarak, 
											![First Page Preview: Multibromo-N-alkylcarbazoles: synthesis, characterization, and their benzo[b]thiophene derivatives Multibromo-N-alkylcarbazoles: synthesis, characterization, and their benzo[b]thiophene derivatives](/preview/png/5266306.png)