𝔖 Bobbio Scriptorium
✦   LIBER   ✦

On the mechanism of alkyl dimer formation in reactions of alkyl iodides with sodium naphthalene. Evidence from reactions of 1,4-diiodobutane.

✍ Scribed by John F. Garst; John T. Barbas


Publisher
Elsevier Science
Year
1969
Tongue
French
Weight
236 KB
Volume
10
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


Recent studies indicate that the initial reactions of alkyl halides with sodium naphthalene in IME are best regarded as dissociative electron-transfer reactions, with no significant competition from nucleophilic displacement reactions (Eq. 1) (1,Za). The initially-formed m + :Naph:,Na+ -R*


πŸ“œ SIMILAR VOLUMES


On the Mechanism of the Reactions of 4-A
✍ Gerrit L'abbΓ©; Ernestine Albrecht πŸ“‚ Article πŸ“… 2010 πŸ› Wiley (John Wiley & Sons) βš– 108 KB πŸ‘ 1 views

Although the first cycloaddition-elimination reactions of 4-alkyl-5-arylimino-1,2,3,4-thiatriazolines (1) with heterocumulenes were reported in 1976-78,' insight into the mechanistic puzzle has been gained recently, and then only for isothiocyanates.2 For isocyanates, which furnish l ,2,4-thiadiazol