Asymmetric Olefin Isomerization via Phase-Transfer-Catalyzed [1,3]-Hydrogen Transfer for Access to Axially Chiral Furan-Benzimidazoles
An efficient catalytic asymmetric olefin isomerization of axially chiral methylene dihydrofuran-benzimidazoles via kinetic resolution is reported. Under mild phase-transfer catalysis, axially chiral furan-benzimidazole compounds and recovered methylene dihydrofuran-benzimidazoles were obtained in high ee. The combination of the kinetic resolution and TBD-catalyzed isomerization of recovered dihydrofuran-benzimidazoles provided access to both enantiomers of furan-benzimidazoles. Deuterium-labeling experiments reveal intramolecular [1,3]-H transfer mechanism. The utility of this method was demonstrated by scale-up synthesis and functionalization of the products.
Authors
- Dong‐Chao Wang (ORCID: https://orcid.org/0000-0002-5037-4727)
- Kaili Ma (ORCID: https://orcid.org/0000-0003-0394-6566)
- Hai‐Ming Guo (ORCID: https://orcid.org/0000-0003-0629-4524)
- Yu‐Qing Guan
Institutions
- Henan Normal University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-05-09
- DOI
- https://doi.org/10.1021/acs.orglett.5c01181
- Citations
- 5
- Primary Topic
- Axial and Atropisomeric Chirality Synthesis
- Type
- article
- Field-Weighted Citation Impact
- 4.68
Funders
- National Natural Science Foundation of China
- Natural Science Foundation of Henan Province
- Henan Key Laboratory of Organic Functional Molecules and Drug Innovation