Dataset of Enabling Cyclization Strategies through Carbonyl Ylide Mediated Synthesis of Malonate Enol Ethers

Malonate enol ethers are afforded in one step by condensation of cyclic ketones with α-diazomalonates under [CpRu(CH3CN)3][BArF] catalysis. Thanks to the dual reactivity of these 2-vinyloxymalonates, a range of orthogonal cyclizations is enabled that extends remarkably the scope of annulations from carbonyl ylide intermediates.

    Organizational unit
    Laboratory of Professor Jérôme Lacour
    Creative Commons Attribution 4.0 International
Publication date16/03/2021
Retention date26/04/2031
accessLevelPublicAccess levelPublic
duaNoneContract on the use of data
  • Viñas-Lóbez, Júlia
  • Levitre, Guillaume orcid
  • de Aguirre, Adiran
  • Besnard, Céline orcid
  • Poblador Bahamonde, Amalia orcid
  • Lacour, Jérôme orcid
  • Quality (0 Reviews)
  • Usefulness (0 Reviews)

Datacite metadata

Packages information

Similar archives

Laboratory of Professor Jérôme Lacour
Dataset of Organic & Biomolecular Chemistry_Aliphatic amide macrocycles
2019 accessLevelPublic Public 1.6 GB
Laboratory of Professor Jérôme Lacour
Dataset of submission_Photo-Induced Thiol-Ene Reactions of Unsaturated Polyether Macrocycles
2019 accessLevelPublic Public 1016.2 MB
Laboratory of Professor Jérôme Lacour
Multistate Aggregation-Induced Chiroptical Properties of Enantiopure Disulfide-Mediated BisPyrene Macrocycles
2022 accessLevelPublic Public 151.2 MB
Laboratory of Professor Jérôme Lacour
Regiodivergent Synthesis of Oxadiazocines via Dirhodium-Catalyzed Reactivity of Oxazolidines and alpha-Imino Carbenes
2023 accessLevelPublic Public 1.1 GB
All rights reserved by DLCM and the University of GenevaunigeBlack