Asymmetric Transfer Hydrogenation of gem ‐Difluorocyclopropenyl Esters: Access to Enantioenriched gem ‐Difluorocyclopropanes
Author:
Affiliation:
1. Molecular, Macromolecular Chemistry, and Materials ESPCI Paris, PSL University CNRS 10 rue Vauquelin 75005 Paris France
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202008572
Reference92 articles.
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4. Experimental Study of the Stereomutation of 1,1-Difluoro-2-ethyl-3-methylcyclopropane Confirms the Predicted Preference for Disrotatory Ring Opening and Closure
5. Structure, Synthesis, and Chemical Reactions of Fluorinated Cyclopropanes and Cyclopropenes
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1. Experimental and Theoretical Studies on Stereomutation Through gem‐Difluorocyclopropanylide Intermediates;Asian Journal of Organic Chemistry;2024-01-15
2. Synthesis of Selectively gem‐Difluorinated Molecules; Chiral gem‐Difluorocyclopropanes via Chemo‐Enzymatic Reaction and gem‐Difluorinated Compounds via Radical Reaction;The Chemical Record;2023-03-22
3. Catalytic Asymmetric Conjugate Reduction;Angewandte Chemie International Edition;2023-02-27
4. Catalytic Asymmetric Conjugate Reduction;Angewandte Chemie;2023-02-27
5. Catalytic Diversification of gem ‐Difluorocyclopropanes: Recent Advances and Challenges;ChemCatChem;2022-09-12
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