ArticleOrganic letters2017
Intramolecular Chirality Transfer [2 + 2] Cycloadditions of Allenoates and Alkenes.
Article in Organic letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed.
- Lewis Acid-Promoted [2 + 2] Cycloadditions of Allenes and Ketenes: Versatile Methods for Natural Product Synthesis.Accounts of chemical research · 2023Article
- Unveiling the Chemistry and Synthetic Potential of Catalytic Cycloaddition Reaction of Allenes: A Review.Molecules (Basel, Switzerland) · 2023Review
- Stereoselective [2+2]-Cycloadditions of chiral allenic ketones and alkenes: Applications towards the synthesis of benzocyclobutenes and endiandric acids.Tetrahedron · 2022Article
- Enantioselective Synthesis of (+)-Hippolide J and Reevaluation of Antifungal Activity.Organic letters · 2020Article
- Evolution of a Strategy for the Enantioselective Synthesis of (-)-Cajanusine.Journal of the American Chemical Society · 2020Article
- Lessons in Strain and Stability: Enantioselective Synthesis of (+)-[5]-Ladderanoic Acid.Angewandte Chemie (International ed. in English) · 2020Article
- Recent advances in the synthesis of gem-dimethylcyclobutane natural products.Natural product reports · 2019Review
- Photo-editable macromolecular information.Nature communications · 2019Article
- Thioallenoates in Catalytic Enantioselective [2+2]-Cycloadditions with Unactivated Alkenes.Tetrahedron · 2019Article
- Allenoates in Enantioselective [2+2] Cycloadditions: From a Mechanistic Curiosity to a Stereospecific Transformation.Journal of the American Chemical Society · 2018Article
- Synthesis of (-)-Hebelophyllene E: An Entry to Geminal Dimethyl-Cyclobutanes by [2+2] Cycloaddition of Alkenes and Allenoates.Angewandte Chemie (International ed. in English) · 2018Article
- Synthesis of ent-[3]-Ladderanol: Development and Application of Intramolecular Chirality Transfer [2+2] Cycloadditions of Allenic Ketones and Alkenes.Journal of the American Chemical Society · 2017Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
Intramolecular chirality transfer [2 + 2] cycloaddition of enantiomerically enriched allenoates and alkenes is presented. The use of a chiral catalyst was found to be critical to achieve high levels of diastereoselectivity compared to use of an achiral catalyst. The method developed leads to highly substituted cyclobutanes that would be difficult to prepare by alternative methods.
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Registered trials
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