N-Arylation

Andrew Martins, Sébastien Lemouzy and Mark Lautens* ... The following key references were inadvertently omitted from the text: (a) Bertolini, F.; Mac...
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ORGANIC LETTERS 2009 Vol. 11, No. 5 1191

Additions and Corrections Volume 8, 2006

Volume 11, 2009

Shuzhi Dong, Gregory D. Parker, Takahiro Tei, and Leo A. Paquette*

Andrew Martins, Se´bastien Lemouzy, and Mark Lautens*

In Pursuit of Pestalotiopsin A via Zirconocene-Mediated Ring Contraction.

Bifunctional Reactivity of CuI: Sequential Ring Opening/ N-Arylation.

Page 2430. The configurations at C-3 in 4 and its counterpart 5 were inadvertently reversed. As delineated previously (ref 10), the major aldol product 4 (9:1) has the anti configuration, while the minor component 5 is the syn diastereomer. The correct graphic is shown below. All subsequent transformation products should reflect this minor adjustment.

Page 181. The following key references were inadvertently omitted from the text: (a) Bertolini, F.; Macchia, F.; Pineschi, M. Tetrahedron Lett. 2006, 47, 9173. (b) Crotti, S.; Bertolini, F.; Macchia, F.; Pineschi, M. Chem. Commun. 2008, 3127. (c) Pineschi, M.; Del Moro, F.; Crotti, P.; Macchia, F. Org. Lett. 2005, 7, 3605. The authors apologize for this oversight. OL900022K 10.1021/ol900022k Published on Web 01/16/2009

OL900132M 10.1021/ol900132m Published on Web 01/27/2009