Tandem copper-catalysed aryl and alkenyl amination reactions: the synthesis of N-functionalised indoles.
A Cu-diamine complex effectively catalyses tandem C-N bond formation on 2-(2-haloalkenyl)-aryl halide substrates, to deliver a series of N-functionalised indoles. Anilines, amides and carbamates are all effective coupling partners under the developed conditions.
المؤلفون الرئيسيون: | Hodgkinson, R, Schulz, J, Willis, M |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2009
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مواد مشابهة
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Palladium-catalysed tandem alkenyl- and aryl-C-N bond formation: a cascade N-annulation route to 1-functionalised 7-azaindoles
حسب: Hodgkinson, R, وآخرون
منشور في: (2009) -
Copper-catalysed benzofuran synthesis: developing aryl bromide-alkenyl triflates as general heterocycle precursors
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Palladium-catalysed aminosulfonylation of aryl-, alkenyl- and heteroaryl halides: scope of the three-component synthesis of N-aminosulfonamides.
حسب: Emmett, E, وآخرون
منشور في: (2012) -
Palladium-catalyzed tandem alkenyl and aryl C--N bond formation: a cascade N-annulation route to 1-functionalized indoles.
حسب: Willis, M, وآخرون
منشور في: (2005) -
2-(2-haloalkenyl)-aryl halides as substrates for palladium-catalysed tandem C-N bond formation: Efficient synthesis of 1-substituted indoles
حسب: Willis, M, وآخرون
منشور في: (2006)