On the mechanism of formation of dimeric and reduced products from an α-halo amide with sodium methoxide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Anomalous substitutions and reductive dehalogenations of α,α-diaryl-α-halogeno- n,n-dimethylacetamides by methoxide
2. The remarkable reactivity of aryl halides with nucleophiles
3. Substitutionsreaktionen über Radikalanionen
4. Radical chain reductive dehalogenation of hetaryl halides promoted by methoxide ion
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Furofuranonaphthoquinones: bioactive compounds with a novel fused ring system from crescentia cujete;Tetrahedron;1993-07
2. Free Radical Chain Processes in Aliphatic Systems involving an Electron Transfer Reaction;Advances in Physical Organic Chemistry Volume 23;1987
3. Electron transfer processes. 34. Reactions of .alpha.-halo ketones with nucleophiles;Journal of the American Chemical Society;1985-04
4. Single‐electron Transfer‐initiated Thermal Reactions of Arylmethyl Halides, IX. The Reaction of 2‐Bromo‐ N , N ‐dimethyl‐2,2‐diphenylacetamide with Triethylamine in Benzene;Chemische Berichte;1985-03
5. Single-electron transfer-initiated thermal reactions of arylmethyl halides. Part 8. The reaction of 2-halogeno-NN-dimethyl-2,2-diphenylacetamides with sodium methoxide in 2,2-dimethoxypropane. The effects of added acetone, temperature elevation, and of the nature of the halogen. Refinement of the reaction mechanism;J. Chem. Soc., Perkin Trans. 2;1984
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