A series of Mn III porphyrins progressively halogenated in the electrophilic pathway of addition and a stereospecific pathway of oxygen insertion, the former being disfavoured Ξ²-pyrrolic positions was employed to catalyse the epoxidation of cis-stilbene by iodosylbenzene, and to study by electron-wi
β¦ LIBER β¦
Olefin epoxidation by manganese(III)-porphyrin complexes: effect of pyridine on stereoselectivity
β Scribed by Alexander W. Van Der Made; Roeland J.M. Nolte
- Publisher
- Elsevier Science
- Year
- 1984
- Weight
- 169 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0304-5102
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## Abstract The asymmetric epoxidation of unfunctionalised olefins to epoxides is realised by using manganese(III) complexes stabilised on nanocrystalline magnesium oxide in the presence (1__R__,2__R__)β(β)βdiaminocyclohexane as a chiral ligand in good yields and up to 91β% enantiomeric excess.
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