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Pd-catalyzed arylation synthesizes chiral gem-diarylmethyl boronates, suggesting new bioactive compound pathways.
Geminal multiarylmethyl moieties are crucial structural components in a wide variety of bioactive and pharmaceutical compounds. Herein, we present a Pd-catalyzed enantioconvergent arylation of racemic stable solid benzylic α-boryl organozinc reagents, enabling the synthesis of chiral gem-diarylmethyl boronates. In addition, the previously unexplored sterically hindered gem-triarylmethyl boronates were readily accessed via successive dual arylation of benzylboronates. The synthetic practicability of gem-triarylmethyl boronates was demonstrated by their conversion to triaryl methanol, triaryl alkane, and tetraarylmethane derivatives.
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Jin et al. (2026) studied this question.
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