Iridium-catalyzed asymmetric cascade allylation/lactonization of methyl salicylates: enantioselective construction of chiral benzodioxepinones

An efficient asymmetric cascade allylation/lactonization of methyl salicylates is achieved. The utilization of chiral-bridged biphenyl phosphoramidite ligand resulted in good results for the construction of a wide range of chiral benzodioxepinones.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2024-11-05
DOI
https://doi.org/10.1039/d4qo01771d
Citations
6
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.95
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article

Iridium-catalyzed asymmetric cascade allylation/lactonization of methyl salicylates: enantioselective construction of chiral benzodioxepinones

Xiaobo He, Jiang Long, Liqin Qiu, Bendu Pan et al.
6 citations
Organic Chemistry Frontiers
Asymmetric Hydrogenation and Catalysis
0.95
article

Iridium-catalyzed asymmetric cascade allylation/lactonization of methyl salicylates: enantioselective construction of chiral benzodioxepinones

Xiaobo He, Jiang Long, Liqin Qiu, Bendu Pan, Yaqi Zhang, Yunru Wu
article en
6 citations

Abstract

An efficient asymmetric cascade allylation/lactonization of methyl salicylates is achieved. The utilization of chiral-bridged biphenyl phosphoramidite ligand resulted in good results for the construction of a wide range of chiral benzodioxepinones.

Organic Chemistry FrontiersVol. 12(1)
Sun Yat-sen University (CN)
Openalex Percentile: Top 28%
Asymmetric Hydrogenation and Catalysis
0.95
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