Synthesis 2012; 44(24): 3811-3814
DOI: 10.1055/s-0032-1316813
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Indoles by Copper-Catalyzed Heteroannulation of o-Aminophenylboronic Acid Pinacol Esters with β-Keto Esters

Ala Bunescu
Ecole Polytechnique Fédérale de Lausanne, EPFL-SB-ISIC-LSPN, BCH 5304, 1015 Lausanne, Switzerland   Fax: +41(21)6939740   eMail: jieping.zhu@epfl.ch
,
Qian Wang
Ecole Polytechnique Fédérale de Lausanne, EPFL-SB-ISIC-LSPN, BCH 5304, 1015 Lausanne, Switzerland   Fax: +41(21)6939740   eMail: jieping.zhu@epfl.ch
,
Jieping Zhu*
Ecole Polytechnique Fédérale de Lausanne, EPFL-SB-ISIC-LSPN, BCH 5304, 1015 Lausanne, Switzerland   Fax: +41(21)6939740   eMail: jieping.zhu@epfl.ch
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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.

Supporting Information