Kinetics of Rh(II)-Catalyzed α-Diazo-β-ketoester Decomposition and Application to the [3+6+3+6] Synthesis of Macrocycles on a Large Scale and at Low Catalyst Loadings
Author:
Affiliation:
1. Department of Organic Chemistry and ‡Department of Inorganic and Analytical Chemistry, University of Geneva, 30 Quai Ernest Ansermet, CH-1211 Geneva 4, Switzerland
Funder
Université de Genève
Swiss National Science Foundation
Publisher
American Chemical Society (ACS)
Subject
Catalysis,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acscatal.6b01283
Reference54 articles.
1. Domino reactions of diazodicarbonyl compounds with α,β-unsaturated δ-amino esters: a convenient way towards 2-oxopiperidines, dihydropyridinones and isoquinolinediones
2. Novel one-pot synthesis of diverse γ,δ-unsaturated β-ketoesters by thermal cascade reactions of diazodicarbonyl compounds and enol ethers: transformation into substituted 3,5-diketoesters
3. Catalyst- and Halogen-Free Regioselective Friedel-Crafts α-Ketoacylations
4. Synthesis of benzo[a]carbazoles and indolo[2,3-a]carbazoles via photoinduced carbene-mediated C–H insertion reaction
5. Wolff rearrangement of β-alkynyl-α-diazo-β-ketoesters: light-induced acetylene-allene isomerization and its use for activation of enediynes
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