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Asymmetric Evans syn‐Aldol Reactions of Terpene‐Derived Enals: Scope and Limitations

https://doi.org/10.1002/ejoc.201402736
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Outgoing claims: the papers this work cites, builds on, or argues with.

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The Mukaiyama Aldol Reaction: 40 Years of Continuous Development
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Synthesis and Biological Evaluation of Gephyronic Acid Derivatives: Initial Steps towards the Identification of the Biological Target of Polyketide Inhibitors of Eukaryotic Protein Synthesis
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Synthetic studies toward potent cytotoxic agents amphidinolides G and H: Synthesis of the entire C15C26 moiety of the top half
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The Cross-Aldol Reaction of 3-Alkoxy-2-cyclohexen-1-ones with α,β-Enals. A Synthesis of 4-(trans-2-Butenylidene)-3,5,5-trimethyl-2-cyclohexen-1-ones
inferredcites →https://doi.org/10.1246/cl.1973.1011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121629openalex-snapshot
Oxazolidinones as chiral auxiliaries in asymmetric aldol reaction applied to natural products total synthesis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154102openalex-snapshot
Synthesis of (1Z)-deacylcnicin
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01219openalex-snapshot
Samarium Iodide-Promoted Asymmetric Reformatsky Reaction of 3-(2-Haloacyl)-2-oxazolidinones with Enals
inferred← citeshttps://doi.org/10.1039/c8cc06185hopenalex-snapshot
Asymmetric total synthesis of pleurospiroketals A and B
inferred← citeshttps://doi.org/10.1055/a-1643-5729openalex-snapshot
Unified Approach to ent-Eudesmane-Type Terpenoid Synthesis: Total Synthesis of Sinupol and Eutyscoparin A
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