Primary alkyl bis-catecholato silicates in dual photoredox/nickel catalysis: aryl- and heteroaryl-alkyl cross coupling reactions

Abstract : Primary alkyl bis-catecholato silicates have been successfully engaged with aryl and heteroaryl bromide substrates in photoredox/nickel dual catalysis to provide aryl- and heteroaryl-alkyl cross coupling products. The scope of the transformation is wide and the process appears to be tolerant of various functional groups present. Of note, most examples rely on the challenging use of highly reactive primary radicals which constitutes a significant advance in these cross coupling reactions.
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Christophe Lévêque, Ludwig Chenneberg, Vincent Corcé, Jean-Philippe Goddard, Cyril Ollivier, et al.. Primary alkyl bis-catecholato silicates in dual photoredox/nickel catalysis: aryl- and heteroaryl-alkyl cross coupling reactions . Organic Chemistry Frontiers, Royal Society of Chemistry, 2016, 3 (4), pp.462-465. ⟨10.1039/C6QO00014B ⟩. ⟨hal-01278421⟩

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