One-step synthesis of [15]paracyclophane and [16]paracyclophane via Pd-catalyzed C(sp2)–C(sp3) coupling and the cyclohexane-encapsulating crystal structure of [16]paracyclophane
Abstract Macrocycles consisting of methylene-bridged aromatic rings had been synthesized by aromatic electrophilic substitution reactions, thus limiting the substrates to electron-rich aromatic compounds. In this work, we developed a novel method for 1-step synthesis of [15]paracyclophane (PCP) and [16]PCP by the self-condensation of 4-bromobenzyl bromide via a Pd-catalyzed desulfinative coupling reaction between C(sp2) and C(sp3) carbon atoms. In the crystal structure, [16]PCP encapsulated cyclohexane and formed a 1D columnar structure
Authors
- Kenta Rakumitsu (ORCID: https://orcid.org/0000-0002-7905-0961)
- Daichi Takahashi (ORCID: https://orcid.org/0000-0002-2957-8733)
- Sotaro Kusumoto (ORCID: https://orcid.org/0000-0002-7501-383X)
- Akihiro Yokoyama (ORCID: https://orcid.org/0000-0003-3831-8260)
Institutions
- Kanagawa University (JP)
- Seikei University (JP)
Publication Details
- Journal
- Chemistry Letters
- Published
- 2024-10-01
- DOI
- https://doi.org/10.1093/chemle/upae184
- Citations
- 1
- Primary Topic
- Supramolecular Chemistry and Complexes
- Type
- article
- Field-Weighted Citation Impact
- 0.25
Funders
- Seikei University
- Japan Society for the Promotion of Science