ArticleOrganic letters2013
An efficient synthesis of the fully elaborated isoindolinone unit of muironolide A.
Article in Organic letters, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Total Synthesis of Allocyclinone A via Late-Stage Halogen Swapping.Angewandte Chemie (International ed. in English) · 2026Article
- Enantioselective synthesis of (-)-maoecrystal V by enantiodetermining C-H functionalization.Journal of the American Chemical Society · 2014Article
- The chemistry of isoindole natural products.Beilstein journal of organic chemistry · 2013Review
- Total synthesis of maoecrystal V: early-stage C-H functionalization and lactone assembly by radical cyclization.Journal of the American Chemical Society · 2013Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
An efficient stereocontrolled construction of the fully substituted isoindolone subunit of muironolide A is described. The approach is centered on the intramolecular Diels-Alder reaction between the enol form of the β-keto amide and an α,β,γ,δ-unsaturated ester, followed by the installation of the cyclohexene double bond.
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Registered trials
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