Issue 74, 2012

Highly enantioselective Friedel–Crafts alkylation of indoles and pyrrole with β,γ-unsaturated α-ketoesters catalyzed by heteroarylidene-tethered bis(oxazoline) copper complexes

Abstract

The simple and cheap chiral catalyst, heteroarylidene-tethered Ph-bis(oxazoline)–Cu(OTf)2, can efficiently catalyze the asymmetric F–C alkylation of indoles and pyrrole with β,γ-unsaturated α-ketoesters. The 3-indolyl adducts were obtained in up to >99% ee. Moreover, the 2-pyrrolyl adducts were achieved in up to 92% ee for the first time.

Graphical abstract: Highly enantioselective Friedel–Crafts alkylation of indoles and pyrrole with β,γ-unsaturated α-ketoesters catalyzed by heteroarylidene-tethered bis(oxazoline) copper complexes

Supplementary files

Article information

Article type
Communication
Submitted
05 Jul 2012
Accepted
26 Jul 2012
First published
26 Jul 2012

Chem. Commun., 2012,48, 9281-9283

Highly enantioselective Friedel–Crafts alkylation of indoles and pyrrole with β,γ-unsaturated α-ketoesters catalyzed by heteroarylidene-tethered bis(oxazoline) copper complexes

L. Liu, H. Ma, Y. Xiao, F. Du, Z. Qin, N. Li and B. Fu, Chem. Commun., 2012, 48, 9281 DOI: 10.1039/C2CC34803A

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