Chiral monomers, bearing different quinidine derivatives, were copolymerized with achiral monomers, producing insoluble copolymers which were used for the dihydroxylation of styrene as standard substrate. The structure of the polymeric insoluble support was found to be of great importance in determi
โฆ LIBER โฆ
Asymmetric Dihydroxylation of Alkenes
โ Scribed by Mark C. Noe; Michael A. Letavic; Sheri L. Snow
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 8 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
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## Abstract For Abstract see ChemInform Abstract in Full Text.
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Preliminary studies using the chiral title catalyst reveal that the rates are comparable with those of the homogeneous asymmetric dihydroxylation of alkenes. However, the e.e. values are lower. -