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Thermodynamics of the Isomerization of Monoterpene Epoxides
Julián E. Sánchez-Velandia
, Jaime Andrés Becerra
,
Sol M. Mejía
, Aída L. Villa
, Fernando Martínez O
Department of Chemistry
Sustainable use of natural resources
Universidad de Antioquia
Universidad Javeriana
Universidad Industrial de Santander
Research output
:
Contribution to journal
›
Article
›
peer-review
9
Scopus citations
Overview
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Keyphrases
Thermodynamics
100%
Pinene
100%
Monoterpenes
100%
Epoxides
100%
Isomerization
100%
Group Contribution Method
75%
MCM-41
75%
Epoxide Isomerization
75%
Gibbs Free Energy
50%
Aldehydes
50%
Alcohol
25%
Density Functional Theory
25%
Campholenic Aldehyde
25%
Monoterpenoids
25%
Ketones
25%
PBE-D3
25%
Computational Chemistry
25%
Transcranial Focused Ultrasound (tFUS)
25%
Catalytic Reaction
25%
Oxygenated Compounds
25%
Isomerization Reaction
25%
Heat of Reaction
25%
Cu-MCM-41
25%
Perillyl Alcohol
25%
Evaluated Temperature
25%
Thermodynamic Analysis
25%
Density Functional Calculations
25%
Ethyl Acetate
25%
Fe-MCM-41
25%
Chemistry
Isomerization
100%
Monoterpene
100%
Epoxide
100%
Thermodynamics
100%
Terpene
100%
Pinene
66%
Aldehyde
50%
Gibbs Free Energy
33%
Density Functional Theory
33%
Monoterpenoid
16%
Heat Capacity Cv
16%
Computational Chemistry
16%
Thermodynamic Analysis
16%
Pc
16%
Ketones
16%
Heat of Reaction
16%
Perillyl Alcohol
16%
Enthalpy
16%
Ethyl Acetate
16%
Catalytic Reaction
16%
INIS
thermodynamics
100%
isomerization
100%
epoxides
100%
transformations
50%
solvents
50%
aldehydes
50%
data
33%
alcohols
33%
density functional method
33%
gibbs free energy
33%
range
16%
chemistry
16%
comparative evaluations
16%
yields
16%
enthalpy
16%
ketones
16%
heat of reaction
16%
acetates
16%