4.4 Article

Synthesis of 1-arylidene-2,3-dihydro-1H-inden-2-ols through a tandem carbopalladation/Suzuki-Miyaura sequence

Journal

TETRAHEDRON LETTERS
Volume 49, Issue 23, Pages 3713-3715

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2008.04.042

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A regio- and stereoselective synthesis of arylidene indenols has been developed. The key step involves a palladium-catalyzed tandem carbocyclization/Suzuki-Miyaura sequence. (C) 2008 Elsevier Ltd. All rights reserved.

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