Synthesis of a dicyclobutylideneethane derivative via sequential palladium-catalyzed Miyaura borylation and Suzuki coupling

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Abstract

An efficient synthesis of a dicyclobutylideneethane derivative was achieved using a palladium-catalyzed reaction of a substituted (bromomethylene)cyclobutane with bis(pinacolato)diboron. The reaction mechanism was investigated in detail. The Suzuki cross-coupling reaction of a (bromomethylene)cyclobutane with arylboronic acid was also achieved. © 2003 Elsevier Ltd. All rights reserved.

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Kabalka, G. W., & Yao, M. L. (2003). Synthesis of a dicyclobutylideneethane derivative via sequential palladium-catalyzed Miyaura borylation and Suzuki coupling. Tetrahedron Letters, 44(43), 7885–7887. https://doi.org/10.1016/j.tetlet.2003.09.018

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