Exploring Diradical Chemistry: A Carbon-Centered Radical May Act as either an Anion or Electrophile through an Orbital Isomer
Author:
Publisher
Wiley
Subject
General Medicine
Reference73 articles.
1. Concerted Reactions That Produce Diradicals and Zwitterions: Electronic, Steric, Conformational, and Kinetic Control of Cycloaromatization Processes
2. p-Benzyne. Generation as an intermediate in a thermal isomerization reaction and trapping evidence for the 1,4-benzenediyl structure
3. Reactive 1,4-dehydroaromatics
4. Evidence for the reactive spin state of 1,4-dehydrobenzenes
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2. Drawing Catalytic Power from Charge Separation: Stereoelectronic and Zwitterionic Assistance in the Au(I)-Catalyzed Bergman Cyclization;Journal of the American Chemical Society;2017-02-22
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4. Four-Electron Electrocyclic Ring-Opening/Intermolecular [4+2] Cycloadditions of α-Hydroxycyclobutenones: Stereoselective Synthesis of Multiple Substituted δ-Lactams;Advanced Synthesis & Catalysis;2016-03-17
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