Modular Synthesis of Geminal Triarylmethyl and Chiral Diarylmethyl Boronates via Arylation of Solid α-Boryl Organozinc Reagents
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 <i>gem</i>-diarylmethyl boronates. In addition, the previously unexplored sterically hindered <i>gem</i>-triarylmethyl boronates were readily accessed via successive dual arylation of benzylboronates. The synthetic practicability of <i>gem</i>-triarylmethyl boronates was demonstrated by their conversion to triaryl methanol, triaryl alkane, and tetraarylmethane derivatives.
Authors
- Miao Zhan (ORCID: https://orcid.org/0000-0002-6492-5104)
- Liang Xu (ORCID: https://orcid.org/0000-0002-7939-8108)
- Xin An (ORCID: https://orcid.org/0009-0002-7544-1452)
- Shuda Luo
- Hao Jin
Institutions
- Shihezi University (CN)
- Northwestern Polytechnical University (CN)
- Shenzhen Polytechnic University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-01-21
- DOI
- https://doi.org/10.1021/acs.orglett.5c04535
- Primary Topic
- Organoboron and organosilicon chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00