Search results for "Mononuclear Heterocyclic Rearrangement"

showing 2 items of 2 documents

Unexpected Substituent Effects in the Iso-Heterocyclic Boulton-Katritzky Rearrangement of 3-Aroylamino-5-methyl-1,2,4-oxadiazoles: A Mechanistic Stud…

2019

The kinetics of the iso-heterocyclic mononuclear rearrangement of some 3-aroylamino-5-methyl-1,2,4-ozadiazoles was carefully examined under largely variable acidic or alkaline conditions. This reaction may proceed via two different mechanistic pathways (an uncatalyzed and a base-catalyzed one), as accounted for also by the evaluation of the relevant activation parameters. Substituent effects, as quantified by means of the Hammett’s equation, appear relatively modest; however, they reveal some interesting anomalies, which enabled us to draw a very precise picture of the intimate reaction course.

010304 chemical physicsChemistryKineticsSubstituent124-oxadiazoleSettore CHIM/06 - Chimica OrganicaMononuclear Heterocyclic Rearrangement010402 general chemistry01 natural sciences0104 chemical sciencesKineticschemistry.chemical_compoundSubstituent effectComputational chemistry0103 physical sciencesPhysical and Theoretical ChemistryReaction mechanismThe journal of physical chemistry. A
researchProduct

The synthesis of fluorinated heteroaromatic compounds. Part 2. Five-membered rings with two heteroatoms. A review

2007

DAKIN-WEST REACTIONCONVENIENT SYNTHESISPOLYFUNCTIONALLY SUBSTITUTED PYRAZOLESOrganic ChemistryTRIFLUOROMETHYL-BETA-DIKETONESN-DIFLUOROMETHYL ANIONSMONONUCLEAR HETEROCYCLIC REARRANGEMENTSHALOACETYLATED ENOL ETHERSF-19 NMR-SPECTRAELECTROLYTIC PARTIAL FLUORINATIONALPHA-AMINO-ACIDS
researchProduct