Aryl versus Alkyl Redox-Active Diazoacetates ─ Light-Induced C–H Insertion or 1,2-Rearrangement
Author:
Affiliation:
1. Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44, 5201-224 Warsaw, Poland
Funder
Narodowe Centrum Nauki
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c02055
Reference39 articles.
1. Recent advances in transition-metal-catalyzed carbene insertion to C–H bonds
2. Enantioselective carbenoid insertion into C(sp3)–H bonds
3. Visible light-promoted reactions with diazo compounds: a mild and practical strategy towards free carbene intermediates
4. Diazo Compounds: Versatile Synthons for the Synthesis of Nitrogen Heterocycles via Transition Metal-Catalyzed Cascade C-H Activation/Carbene Insertion/Annulation Reactions
5. Application of donor/acceptor-carbenoids to the synthesis of natural products
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1. Visible-Light-Promoted N–H Insertion/Controllable Transformation of Diazoalkanes and 3-Aminomethylated Maleimides;The Journal of Organic Chemistry;2024-09-05
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