Revisiting Aromatic Claisen Rearrangement Using Unstable Aryl Sulfonium/Iodonium Species: The Strategy of Breaking Up the Whole into Parts
Author:
Affiliation:
1. Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Zhejiang Normal University, 688 Yingbin Road, Jinhua321004, China
Funder
National Natural Science Foundation of China
Natural Science Foundation of Zhejiang Province
Publisher
American Chemical Society (ACS)
Subject
General Medicine,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.accounts.2c00263
Reference95 articles.
1. Redox-Neutral α-Arylation of Alkyl Nitriles with Aryl Sulfoxides: A Rapid Electrophilic Rearrangement
2. Dearomative Dual Functionalization of Aryl Iodanes
3. Asymmetric Iodonio-[3,3]-Sigmatropic Rearrangement to Access Chiral α-Aryl Carbonyl Compounds
4. Morita–Baylis–Hillman‐Type [3,3]‐Rearrangement: Switching from Z ‐ to E ‐Selective α‐Arylation by New Rearrangement Partners
5. Über Umlagerung von Phenol‐allyläthern in C ‐Allyl‐phenole
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