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Intermediates in nucleophilic aromatic substitution. Part V. Kinetic versus thermodynamic control in the reactions of methoxide ion with nitrocyanoanisoles; rearrangement of 1,3-to 1,1-dimethoxycyclohexadienylides

โœ Scribed by E.J. Fendler; C.E. Griffin; J.H. Fendler


Publisher
Elsevier Science
Year
1968
Tongue
French
Weight
207 KB
Volume
9
Category
Article
ISSN
0040-4039

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Aromatic nucleophilic substitution VIII.
โœ S. Sekiguchi; T. Takei; T. Aizawa; K. Okada ๐Ÿ“‚ Article ๐Ÿ“… 1977 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 200 KB

Ever since Servis' first observed by NMR spectrometry that in DMSO much faster formation of 1,3\_disubstituted anionic o complex (hereinafter referred to as 1,3-adduct) from 2,4,6\_trinitroanisole (TNA) and 'OCH3 is followed by a much slower attack on the l-position, considerable attention has been