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.

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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

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article

Asymmetric Olefin Isomerization via Phase-Transfer-Catalyzed [1,3]-Hydrogen Transfer for Access to Axially Chiral Furan-Benzimidazoles

Dong‐Chao Wang, Kaili Ma, Hai‐Ming Guo, Yu‐Qing Guan
5 citations
Organic Letters
Axial and Atropisomeric Chirality Synthesis
4.68
article

Asymmetric Olefin Isomerization via Phase-Transfer-Catalyzed [1,3]-Hydrogen Transfer for Access to Axially Chiral Furan-Benzimidazoles

Dong‐Chao Wang, Kaili Ma, Hai‐Ming Guo, Yu‐Qing Guan
article en
5 citations

Abstract

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.

Organic LettersVol. 27(20)
Henan Normal University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Henan Province, Henan Key Laboratory of Organic Functional Molecules and Drug Innovation
Openalex Percentile: Top 6%
Axial and Atropisomeric Chirality Synthesis
4.68
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