Copper-catalysed benzofuran synthesis: developing aryl bromide-alkenyl triflates as general heterocycle precursors
A range of conjugated aryl bromide-alkenyl triflates, previously described as indole precursors, are efficiently converted to the corresponding benzofurans when treated with CuI/TMEDA and potassium hydroxide. © 2007 Elsevier Ltd. All rights reserved.
Главные авторы: | Tadd, A, Fielding, MR, Willis, M |
---|---|
Формат: | Journal article |
Язык: | English |
Опубликовано: |
2007
|
Схожие документы
-
Intramolecular palladium-catalyzed direct arylation of alkenyl triflates.
по: Cruz, A, и др.
Опубликовано: (2007) -
Tandem copper-catalysed aryl and alkenyl amination reactions: the synthesis of N-functionalised indoles.
по: Hodgkinson, R, и др.
Опубликовано: (2009) -
Cascade palladium-catalyzed alkenyl aminocarbonylation/ intramolecular aryl amidation: an annulative synthesis of 2-quinolones.
по: Tadd, A, и др.
Опубликовано: (2009) -
Cascade Palladium- and Copper-Catalysed Aromatic Heterocycle Synthesis: The Emergence of General Precursors
по: Ball, C, и др.
Опубликовано: (2013) -
Palladium catalysed aryl enol ether synthesis from vinyl triflates.
по: Willis, M, и др.
Опубликовано: (2003)