A new, highly selective type of radical chlorination
โ Scribed by F. Minisci; R. Galli; A. Galli; R. Bernardi
- Publisher
- Elsevier Science
- Year
- 1967
- Tongue
- French
- Weight
- 39 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
In polychloro-2,2-difluoropropanes, where a large inductive effect results in relatively low reactivity to chlorination, the presence of additional chlorine causes an increased reactivity of the hydrogens geminal to the chlorine and a reduced reactivity of the remote (third carbon) hydrogens. The wa
The prevalent nucleophilic character of the alkyl radicals' readily permits thehomolyticalkylation of protonated heteroaromatic bases2, due to the contribution of polar forms in the transition state: The oxygen atom of ethersand alcohols as well as the nitrogen of amides and amines, attached to the