Issue 24, 1995
From the journal:

Journal of the Chemical Society, Chemical Communications

A novel and efficient route to (E)-alk-1-enyl boronic acid derivatives from (E)-1-(trimethylsilyl)alk-1-enes and a formal Suzuki–Miyaura cross-coupling reaction starting with vinylsilanes

Gianluca M. Farinola,   Vito Fiandanese,   Luigia Mazzone  and  Francesco Naso  

Abstract

A novel and highly efficient conversion of vinylsilanes into vinyl boronates is described together with their Suzuki–Miyaura cross-coupling reaction, performed without isolating the intermediate resulting from borodesllyiation.

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Article information

DOI
https://doi.org/10.1039/C39950002523
Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 2523-2524

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A novel and efficient route to (E)-alk-1-enyl boronic acid derivatives from (E)-1-(trimethylsilyl)alk-1-enes and a formal Suzuki–Miyaura cross-coupling reaction starting with vinylsilanes

G. M. Farinola, V. Fiandanese, L. Mazzone and F. Naso, J. Chem. Soc., Chem. Commun., 1995, 2523 DOI: 10.1039/C39950002523

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