Reply to Correspondence on “Carbon‐Centered Radical Addition to O=C of Amides or Esters as a Route to C−O Bond Formations”
Author:
Affiliation:
1. College of Chemistry and Molecular SciencesWuhan University Wuhan 430072 P.R. China
Publisher
Wiley
Subject
General Chemistry,Catalysis,Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201805351
Reference20 articles.
1. Carbon-Centered Radical Addition to OC of Amides or Esters as a Route to CO Bond Formations
2. An abnormal photo-fries rearrangement of aryl phthalates
3. Study of 5-Endo Cyclization of 5-Oxapenta-2,4-dienoyl Radical and Related Radicals by ab Initio Calculations. Unusual Nonradical Cyclization Mechanism
4. Mechanism of Reduction of Alkyl Halides by Organotin Hydrides
5.
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1. Photoredox-catalyzed oxytrifluoromethylation of alkenes toward CF3-containing five-membered cyclic carbonates;Organic Chemistry Frontiers;2024
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3. A Desaturase‐Like Enzyme Catalyzes Oxazole Formation in Pseudomonas Indolyloxazole Alkaloids;Angewandte Chemie;2021-03-05
4. Iron-Catalyzed [2+2+2] Annulation of Aliphatic Bridged 1,n -Enynes with Aldehydes for the Synthesis of Fused Pyrans;European Journal of Organic Chemistry;2020-05-28
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