Bunnett and his coworkers1 have successfully carried out many nucleophilic substitution reactions on simple halobeneenes under stimulation eitner by ammoniated electrons or light (around 300-380 nm) . These reactions according to them proceed via SDNl mechanism2. very ret ently
Mesitylation and phenylation of picolyl anions by the SRN1 mechanism
β Scribed by Bunnett, J. F.; Gloor, Bernhard F.
- Book ID
- 126898377
- Publisher
- American Chemical Society
- Year
- 1974
- Tongue
- English
- Weight
- 400 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0022-3263
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π SIMILAR VOLUMES
The ~afion of N-acetylthiomorpholinΒ’ 2 was studied in photostimdated reactions with iodobenzene la and l-iodonaphthalene lb in DMSO, giving good yields of the substitution products 3a and 3b by the SR~I mechanism. The reaction of la with 2 is also induced with FeBr2. l-Iodoadamantane 4 did not react
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