Evidence for Electron-transfer Process in Abnormal Grignard Reactions. Enolization and α-Diketone Formation
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/53/10/53_10_3029/_pdf
Reference11 articles.
1. Eetyl Radical Formed in the Grignard Reaction of 2-Methylbenzophenone
2. Abnormal Grignard Reaction of 2,4,6-Trimethylbenzophenone: An Electron-transfer Mechanism
3. Ketyl Radicals Formed in Grignard Reaction. III. Steric Effects on the Formation of Radicals
4. Ketyl Radicals Formed in Grignard Reaction. IV. Sterically Hindered Ketyl Radicals in Nuclear Replacement and Conjugate Addition
5. The Tautomerism of Certain Derivatives of Acetomesitylene
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1. Synthesis of α,α-diarylacetamides from benzyl aryl ketones using 2-azido-1,3-dimethylimidazolinium hexafluorophosphate;Tetrahedron Letters;2011-06
2. Reaction of aryliminodimagnesium with diphenyl diketones: Heat evolution accompanying single electron transfer and chelate formation, and product distribution;Journal of Physical Organic Chemistry;1990-06
3. References;Reactivity and Structure Concepts in Organic Chemistry;1983
4. The Replacement of Electronegative Substituents by an Electron-transfer Mechanism. The Factors Governing the Reaction of Carbonyl and Imino Compounds with Organomagnesium Reagents;Bulletin of the Chemical Society of Japan;1982-04
5. ChemInform Abstract: EVIDENCE FOR ELECTRON-TRANSFER PROCESS IN ABNORMAL GRIGNARD REACTIONS. ENOLIZATION AND α-DIKETONE FORMATION;Chemischer Informationsdienst;1981-01-20
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