Stereoselective insertion of cyclopropenes into Mg–Mg bonds
Author:
Affiliation:
1. Department of Chemistry, Molecular Sciences Research Hub, Imperial College London, 82 Wood Lane, Shepherds Bush, London, W12 0BZ, UK
2. Shenzhen Bay Laboratory, Shenzhen, 518132, P. R. China
Abstract
Funder
Leverhulme Trust
China Scholarship Council
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2022/CC/D2CC02931F
Reference28 articles.
1. I. Ueber die Abhängigkeit der verschiedenen Vertretbarkeit des Radicalwasserstoffs in den isomeren Buttersäuren
2. Catalytic Enantioselective Hydroboration of Cyclopropenes
3. Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions
4. Catalytic Enantioselective Hydrostannation of Cyclopropenes
5. Cobalt-Catalyzed Diastereoselective and Enantioselective Hydrosilylation of Achiral Cyclopropenes
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1. Reductive Dimerization of Alkenes and Allenes Enabled by Photochemically Activated Zinc–Zinc Bonded Compounds;Journal of the American Chemical Society;2024-07-03
2. Reductive Metallation of Dendralenes and Myrcene Using Dimagnesium(I) Compounds: A Facile Route to Unsaturated Organomagnesium Compounds;Chemistry – A European Journal;2023-12-07
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