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Photostimulated reactions of haloarenes with 2-naphtylamide ions. A facile synthesis of 1-aryl-2-naphthylamines.

✍ Scribed by A.B. Pierini; M.T. Baumgartner; R.A. Rossi

Publisher
Elsevier Science
Year
1987
Tongue
French
Weight
235 KB
Volume
28
Category
Article
ISSN
0040-4039

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✦ Synopsis

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, (5016) Cbrdoba, Argentina.

πŸ“œ SIMILAR VOLUMES

SRN1 reaction of haloarenes with benzene
SRN1 reaction of haloarenes with benzenethiolate, benzeneselenolate, and benzenetellurolate ions promoted by SmI2
✍ Yongmin Zhang; Hongyun Guo πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 118 KB

## Abstract S~RN~1 reaction is of haloarenes with benzenethiolate, benzeneselenate, and benzenetellurolate ions can be carried out by use of samarium diiodide (SmI~2~) as a promoter in DMF‐THF to afford the corresponding ArZPh compounds in moderate to good yields. Β© 2001 John Wiley & Sons, Inc. Het