Iron-Catalyzed Dearomatization of Biaryl Ynones with Aldehydes via Double C–H Functionalization in Eco-Benign Solvents: Highly Atom-Economical Synthesis of Acylated Spiro[5.5]trienones
Author:
Affiliation:
1. College of Chemistry, Beijing Normal University, Beijing 100875, China
Funder
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c01870
Reference62 articles.
1. Pyrroloiminoquinone and related metabolites from marine sponges
2. Synthesis of Spirocyclic Ethers
3. Discorhabdins and Pyrroloiminoquinone-Related Alkaloids
4. Enantioselective methodologies for the synthesis of spiro compounds
5. Metal Complex Catalysis in the Synthesis of Spirocarbocycles
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1. Regioselective synthesis of N-containing polycyclic compounds via radical annulation cyclization of 1,7-dienes with aldehydes;Chemical Communications;2024
2. BBr3-mediated dearomative spirocyclization of biaryl ynones: facile access to spiro[5.5]dienones;Organic & Biomolecular Chemistry;2024
3. Electrochemical Arene Radical Cation Promoted Spirocyclization of Biaryl Ynones: Access to Alkoxylated Spiro[5,5]trienones;Organic Letters;2023-12-15
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