Selective Suzuki–Miyaura monocoupling reactions of di- and polyhalogenated ethenes and di- and polyhalogenated arene derivatives bearing different or identical halogen atoms are reviewed, and the reasons for the observed stereo-, site- and/or chemo-selectivities are discussed. The use of these reactions as key steps in the synthesis of naturally-occurring compounds, bioactive substances including drugs and liquid crystals is also reported.

Highly selective palladium-catalyzed Suzuki–Miyaura monocoupling reactions of ethene and arene derivatives bearing two or more electrophilic sites

BELLINA, FABIO;LESSI, MARCO
2011-01-01

Abstract

Selective Suzuki–Miyaura monocoupling reactions of di- and polyhalogenated ethenes and di- and polyhalogenated arene derivatives bearing different or identical halogen atoms are reviewed, and the reasons for the observed stereo-, site- and/or chemo-selectivities are discussed. The use of these reactions as key steps in the synthesis of naturally-occurring compounds, bioactive substances including drugs and liquid crystals is also reported.
2011
Rossi, R; Bellina, Fabio; Lessi, Marco
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/144090
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