Asymmetric catalytic oxidation
Asymmetric catalytic oxidation is a technique of oxidizing various substrates to give an enantiopure product using a catalyst.
Reactions
- Jacobsen epoxidation of alkenes using manganese-salen complex and NaOCl
- Sharpless epoxidation of allyl alcohols using titanium isopropoxide, diethyl tartrate, and t-butyl hydroxyperoxide
- Sharpless asymmetric dihydroxylation of alkenes using dihydroquinine or dihydroquinidine ligands on an osmium metal center
- Sharpless oxyamination
- Shi epoxidation of alkenes using oxone and a fructose-derived chiral catalyst
- Sulfonyloxaziridine enolate oxidation
See also
Concepts in asymmetric synthesis | |
|---|---|
| Nomenclature | Chirality, Stereocenter, Stereoisomer, Enantiomer, Diastereomer, Meso compound, Planar chirality, Chiral ligand, Axial chirality |
| Analysis | Optical rotation, Enantiomeric excess, Diastereomeric excess, Chiral derivitizing agents |
| Chiral resolution | Crystallization, Kinetic resolution, Chiral column chromatography |
| Reactions | Asymmetric induction, Chiral pool synthesis, Chiral auxiliaries, Asymmetric catalytic reduction, Asymmetric catalytic oxidation, Organocatalysis, Biocatalysis |
Navigation WikiDoc | WikiPatient | Popular pages | Recently Edited Pages | Recently Added
Pictures
There is no pharmaceutical or device industry support for this site and we need your viewer supported Donations | Editorial Board | Governance | Licensing | Disclaimers | Avoid Plagiarism | Policies
Table of Contents In Alphabetical Order | By Individual Diseases | Signs and Symptoms | Physical Examination | Lab Tests | Drugs
Editor Tools Become an Editor | Editors Help Menu | Create a Page | Edit a Page | Upload a Picture or File | Printable version | Permanent link | Maintain Pages | What Pages Link HereThere is no pharmaceutical or device industry support for this site and we need your viewer supported Donations | Editorial Board | Governance | Licensing | Disclaimers | Avoid Plagiarism | Policies
