From the results reported above, longer reaction times seem to be generally required when electron donating groups are present, although a clear trend of reactivity based on the substituents on the boronic acid does not emerge, and generally satisfying yields are obtained regardless of the organoboranes utilized.
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Efficient and Rapid Arylation of NH₂-Unprotected Bromobisindole Ethanamines via Suzuki-Miyaura Coupling: Generating New Leads Against Leishmania.
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