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
Format: Artikel
Sprache:eng
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Zusammenfassung: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.
ISSN:0366-7022
1348-0715
DOI:10.1246/cl.2002.780