Diastereospecific dihydroxylation and highly efficient asymmetric dihydroxylation kinetic resolution of cis/trans-2,6-dimethylbenzylidenecyclohexane
John M. Gardiner, Marck Nörret, Ian H. Sadler
Abstract
John M. Gardiner, Marck Nörret, Ian H. Sadler
Abstract
Achiral dihydroxylation and catalytic asymmetric dihydroxylation (AD) lead to reaction of only the cis(and not the trans) isomer of 2,6-dimethylbenzylidenecyclohexane, dihydroxylation is diastereoisomer specific and an efficient kinetic resolution is achieved using AD.
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Achiral dihydroxylation and catalytic asymmetric dihydroxylation (AD) lead to reaction of only the cis(and not the trans) isomer of 2,6-dimethylbenzylidenecyclohexane, dihydroxylation is diastereoisomer specific and an efficient kinetic resolution is achieved using AD.
Key concepts: Dihydroxylation, Kinetic resolution, Diastereomer, Chemistry, Stereochemistry, Resolution (logic), Catalysis, Enantioselective synthesis