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Synthesis 2012; 44(24): 3811-3814
DOI: 10.1055/s-0032-1316813
DOI: 10.1055/s-0032-1316813
paper
Synthesis of Indoles by Copper-Catalyzed Heteroannulation of o-Aminophenylboronic Acid Pinacol Esters with β-Keto Esters
Weitere Informationen
Publikationsverlauf
Received: 03. Oktober 2012
Accepted after revision: 30. Oktober 2012
Publikationsdatum:
15. November 2012 (online)

Abstract
Copper-catalyzed coupling of o-aminophenylboronic acid pinacol esters with β-keto esters afforded, under mild base-free oxidative conditions, 2,3-disubstituted indoles featuring a key Chan–Lam-type carbon–carbon bond-forming reaction.
Key words
indole - copper catalysis - Chan–Lam reaction - o-aminophenylboronic ester - β-keto esterSupporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
-
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For recent reviews on indole-containing natural products, see:
For reviews about indole synthesis, see:
For reviews of the Chan–Lam reaction, see:
For formation of aryl–CF3 and alkyne–CF3 bonds, see:
For formation of aryl–CN bonds, see:
For oxidative coupling of arylboronic acids with heteroarenes, see:
β-Keto esters as copper ligands, see:
β-Diketones as copper ligands, see:
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