Steric hindrance as a key factor on proton transfer in the σ-adduct forming reactions of o-substituted anilines with 1,3,5-trinitrobenzene in dimethylsulfoxide-Reference-Cited by-同舟云学术

Steric hindrance as a key factor on proton transfer in the σ-adduct forming reactions of o-substituted anilines with 1,3,5-trinitrobenzene in dimethylsulfoxide

Published:2008-04-11 Issue:10 Volume:139 Page:1191-1195
ISSN:0026-9247
Container-title:Monatshefte für Chemie - Chemical Monthly
language:en
Short-container-title:Monatsh Chem

Author:

Asghar Basim H.

Publisher

Springer Science and Business Media LLC

Subject

General Chemistry

Link

http://link.springer.com/content/pdf/10.1007/s00706-008-0913-5.pdf

Reference24 articles.

1. Rate and equilibrium studies in Jackson-Meisenheimer complexes

2. Crampton MR, Gold V (1967) J Chem Soc B:23

3. Intermediates in nucleophilic aromatic substitution. 20. Rate-limiting proton transfer in the formation of Meisenheimer complexes between 1,3,5-trinitrobenzene and amines. The effect of dimethyl sulfoxide on proton-transfer rates. Relative leaving-group abilities of amines and alkoxide ions

4. The stabilities of Meisenheimer complexes. Part 25. Kinetic studies of the reaction of 1,3,5-trinitrobenzene with aliphatic amines in dimethyl sulphoxide

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