Eetyl Radical Formed in the Grignard Reaction of 2-Methylbenzophenone
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/48/3/48_3_1057/_pdf
Reference6 articles.
1. Organometallic reaction mechanisms. VIII. Detailed description of the mechanism of methylmagnesium bromide addition to 2-methylbenzophenone
2. The Appearance of Free Radicals during Grignard Reactions
3. A radical process in a reaction of a grignard compound
4. The Electron Spin Resonance ofo-Substituted Benzophenone Ketyls
5. A Study of the Reaction between Nitrosobenzene and the Grignard Reagent
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1. ESR and ENDOR Studies of the 2-Methylbenzophenone Anion Radical: Unusual Spin Density Distribution due to a Sterical Hindrance by Methyl Substitution;Bulletin of the Chemical Society of Japan;1993-09
2. Time-resolved resonance raman studies of transient species in the photoenolization of 2-methylbenzophenone and 2-benzylbenzophenone;Chemical Physics Letters;1988-08
3. New methodology in determining evidence for single electron transfer in the reaction of Grignard reagents with ketones;Journal of Organometallic Chemistry;1985-09
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. Photochemistry of cyclopropene derivatives. 20. Deuterium isotope effects in the triplet-induced photochemistry of tetrasubstituted cyclopropenes;Journal of the American Chemical Society;1981-06
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