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Enantioselective oxidation of sulphides by dioxiranes in the presence of bovine serum albumin
- Source :
- Tetrahedron Letters. 30:6233-6236
- Publication Year :
- 1989
- Publisher :
- Elsevier BV, 1989.
-
Abstract
- Oxidation of sulphides by in situ generated dioxiranes in buffered (pH 7.5) aqueous solutions, using bovine serum albumin (BSA) as a chiral auxiliary, affords the corresponding sulphoxides in up to 89% enantiomeric excess (e.e.).
- Subjects :
- chemistry.chemical_classification
Chiral auxiliary
Aqueous solution
biology
Sulfide
organic chemicals
Organic Chemistry
Enantioselective synthesis
Albumin
Biochemistry
chemistry.chemical_compound
chemistry
Dioxirane
Drug Discovery
polycyclic compounds
biology.protein
Organic chemistry
heterocyclic compounds
Bovine serum albumin
Enantiomeric excess
Subjects
Details
- ISSN :
- 00404039
- Volume :
- 30
- Database :
- OpenAIRE
- Journal :
- Tetrahedron Letters
- Accession number :
- edsair.doi...........7fe5d098a1288c3dc6e632af76882154
- Full Text :
- https://doi.org/10.1016/s0040-4039(01)93352-0