Nucleophilic Borylation of Benzyl Halides with Bis(pinacolato)diboron Catalyzed by Palladium(0) Complexes

Nucleophilic borylation of benzyl halides with bis(pinacolato)diboron in the presence of KOAc in toluene was effectively catalyzed by a palladium complex generated in situ from Pd(dba)2 and (4-MeOC6H4)3P, giving the corresponding pinacol benzylboronates in high yields.

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Veröffentlicht in:Chemistry letters 2002-08, Vol.31 (8), p.780-781
Hauptverfasser: Ishiyama, Tatsuo, Oohashi, Zengo, Ahiko, Taka-aki, Miyaura, Norio
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container_title Chemistry letters
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creator Ishiyama, Tatsuo
Oohashi, Zengo
Ahiko, Taka-aki
Miyaura, Norio
description Nucleophilic borylation of benzyl halides with bis(pinacolato)diboron in the presence of KOAc in toluene was effectively catalyzed by a palladium complex generated in situ from Pd(dba)2 and (4-MeOC6H4)3P, giving the corresponding pinacol benzylboronates in high yields.
doi_str_mv 10.1246/cl.2002.780
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source Oxford University Press Journals All Titles (1996-Current)
title Nucleophilic Borylation of Benzyl Halides with Bis(pinacolato)diboron Catalyzed by Palladium(0) Complexes
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