Modular Access to Triarylethylene Units from Arylvinyl MIDA Boronates Using a Regioselective Heck Coupling

A palladium-catalyzed, silver-mediated Heck coupling between arylvinyl MIDA boronate esters and aryl iodides is disclosed. The reaction provides an efficient and modular access to a range of 1,1-diaryl alkenyl MIDA boronates that can be easily transformed into triarylethylene compounds through a Suz...

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Veröffentlicht in:Organic letters 2017-10, Vol.19 (19), p.5046-5049
Hauptverfasser: Khanizeman, R. N, Barde, E, Bates, R. W, Guérinot, A, Cossy, J
Format: Artikel
Sprache:eng
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Zusammenfassung:A palladium-catalyzed, silver-mediated Heck coupling between arylvinyl MIDA boronate esters and aryl iodides is disclosed. The reaction provides an efficient and modular access to a range of 1,1-diaryl alkenyl MIDA boronates that can be easily transformed into triarylethylene compounds through a Suzuki coupling.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.7b02218