Cobalt-Catalyzed Carbonylative Cyclization of Allyl Propargyl Ethers with Benzene-1,3,5-triyl Triformate as the CO Source
Author:
Affiliation:
1. Department of Chemistry; Zhejiang Sci-Tech University, Xiasha Campus; Hangzhou 310018 People's Republic of China
2. Leibniz-Institut für Katalyse e. V.; Universität Rostock; Albert-Einstein-Straβe 29a 18059 Rostock Germany
Funder
Zhejiang Natural Science Fund for YoungScholars
Zhejiang Sci-Tech University
Publisher
Wiley
Subject
Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajoc.201800702/fullpdf
Reference54 articles.
1. A Decade of Advancements in Pauson–Khand‐Type Reactions
2. Catalytic Pauson–Khand-type reactions and related carbonylative cycloaddition reactions
3. Advances in the Pauson-Khand Reaction: Development of Reactive Cobalt Complexes
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1. TFBen (Benzene‐1,3,5‐triyl triformate): A Powerful and Versatile CO Surrogate;The Chemical Record;2021-09-30
2. Palladium-catalyzed [2 + 2 + 1] annulation: access to chromone fused cyclopentanones with cyclopropenone as the CO source;Organic Chemistry Frontiers;2021
3. CARBONYLATIVE SYNTHESIS OF HETEROCYCLIC COMPOUNDS USING CO SURROGATES;TARG HETEROCYCL SYST;2020
4. Benzene-1,3,5-triyl Triformate (TFBen)-Promoted Palladium-Catalyzed Carbonylative Synthesis of 2-Oxo-2,5-dihydropyrroles from Propargyl Amines;Organic Letters;2019-12-20
5. Cobalt-based catalysis for carboxylative cyclization of propargylic amines with CO2 at atmospheric pressure;Journal of CO2 Utilization;2019-12
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