English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

vs. amineconcentration curve upward. The current study has demonstrated convincingly that the nature of the leavingand nonleaving groups governs the reaction mechanism. The contrasting reaction mechanisms have beenrationalized in terms of an intramolecular H-bonding interaction, steric acceleration, and steric inhibition.Key Words : Aminolysis, Mechanism, H-bonding interaction, Steric acceleration, Steric inhibitionIntroductionNucleophilic substitution reactions of esters have inten-sively been investigated due to their importance in biologicalprocesses as well as synthetic applications.

A Kinetic Study on Aminolysis of t-Butyl 4-Pyridyl Carbonate and Related Compounds: Effect of Leaving and Nonleaving Groups on Reaction Mechanism