Photostimulated reaction of aryl iodides with 2-naphthoxide ions by the SRN1 mechanism
β Scribed by A.B Pierini; M.T Baumgartner; R.A Rossi
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 208 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
The photostimulated reactions of aryl iodides with 2-naphthylamide ions in liquid the major substitution product. This reaction is ammonia gave 1-aryl-Z-naphthylamines as proposed to occur by the SRN 1 mechanism of nucleophilic substitution Organica, Facultad de Ciencias Quimicas, Suc.16, C.C.61, (5
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## Abstract magnified image The photostimulated reaction of enolate anions of cyclic aromatic ketones such as substituted indanβ1βones and 3,4βdihydroβ2__H__βnaphthalenβ1βone with __o__βiodoaniline in DMSO affords 1β, 2β, 3β, and 4βmethoxyβ5,10βdihydroindeno[1,2β__b__]indoles (34β40%), 1,2β, 1,4β,