Skip to main navigation
Skip to search
Skip to main content
University of Johannesburg Home
Search content at University of Johannesburg
Home
Scholars
Research entities
Research output
Press/Media
Equipment & facilities
Prestigious awards
Theoretical Evaluation of Epimerization in Diels-Alder Cycloadducts
la
Osman F. Guner
,
Koop Lammertsma
, Peter V. Alston
, Raphael M. Ottenbrite
, Donald D. Shillady
University of Alabama at Birmingham
DuPont
Virginia Commonwealth University
Research output
:
Contribution to journal
›
Article
›
peer-review
7
Citations (Scopus)
Overview
Fingerprint
Fingerprint
Dive into the research topics of 'Theoretical Evaluation of Epimerization in Diels-Alder Cycloadducts
la
'. Together they form a unique fingerprint.
Sort by
Weight
Alphabetically
Keyphrases
Epimerization
100%
Diels-Alder
100%
1,3-dioxane
40%
Sulfone
40%
Phenylsulfonyl
40%
Dioxane
40%
Sulfoxide
40%
Column Chromatography
20%
Aryl Substituents
20%
Trans-1
20%
Attractive Interaction
20%
Torsional Effect
20%
Rotamers
20%
Isopropyl
20%
Piperylene
20%
Electron Repulsion
20%
Sulfonyl Group
20%
Published Data
20%
Sulfonyl
20%
Acrylonitrile
20%
Cis-9
20%
Methylthiol
20%
Acid Catalysis
20%
Ab Initio HF
20%
Silica Gel
20%
Reaction Coordinate
20%
Alkyl Substituents
20%
Sulfinyl Chloride
20%
Lewis Acid Catalysis
20%
Computational Results
20%
Phenylthio
20%
Methylsulfonyl
20%
X-ray Crystallographic Analysis
20%
In Cis
20%
Butyl
20%
1,3-pentadiene
20%
13C NMR
20%
Product Distribution
20%
Electrostatic Effect
20%
Methyl Vinyl Ketone
20%
Steric Effect
20%
Chemistry
Diels-Alder Reaction
100%
Epimerization
100%
1,3-dioxane
40%
Dioxane
40%
Sulfone
40%
Sulfoxide
40%
Butyl Group
20%
13C NMR Spectroscopy
20%
Ketone
20%
Substituent Effect
20%
Substance Spectroscopy
20%
Lewis Acid
20%
Rotamer
20%
Methyl Acrylate
20%
X-Ray Crystallographic Analysis
20%
Sulfonyl Group
20%
Product Distribution
20%
Diastereomer
20%
Acid Catalysis
20%
Column Chromatography
20%
Acrylonitrile
20%