Photocatalytic Decyanative Radical Addition Based on Cyano Group Transfer Mediated by Amine-Ligated Boryl Radicals
Herein, we describe a photocatalytic strategy for decyanative hydrofunctionalization of styrenes with α-heteroatom-substituted acetonitriles. This strategy facilitates the generation of α-heteroatom methyl radicals from acetonitriles through cyano group transfer (CGT) enabled by amine-ligated boryl radicals. The broad applicability of this method is demonstrated by its successful application in late-stage functionalization of bioactive compounds. Combined experimental and computational studies suggest that the strong nucleophilic character of amine-ligated boryl radical is beneficial in facilitating the CGT process.
Authors
- Kazutake Takada (ORCID: https://orcid.org/0000-0001-9876-2510)
- Shuichi Nakamura (ORCID: https://orcid.org/0000-0001-5633-8367)
- Naoki Yasukawa (ORCID: https://orcid.org/0000-0002-7994-0470)
- Yuto Yoshida (ORCID: https://orcid.org/0009-0005-3576-1859)
- Waka Okada
Institutions
- Nagoya Institute of Technology (JP)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-06-24
- DOI
- https://doi.org/10.1021/acs.orglett.5c02217
- Citations
- 5
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 4.68
Funders
- Takahashi Industrial and Economic Research Foundation
- Japan Society for the Promotion of Science