2012
DOI: 10.1016/j.jorganchem.2012.05.002
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Asymmetric epoxidation of unfactionalized olefins catalyzed by chiral salen Mn(III) immobilized onto sulfoalkyl modified zirconium poly(styrene-isopropenyl phosphonate)-phosphate and zirconium poly(styrene-phenylvinyl phosphonate)-phosphate

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Cited by 6 publications
(1 citation statement)
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“…62 2.2.9 Asymmetric epoxidation. [63][64][65][66][67][68][69] Chemical modication of zinc poly(styrene-phenylvinylphosphonate)-phosphate 70 zirconium poly(styrene-isopropenylphosphonate)-phosphate, 71,72 followed by attachment of a chiral manganese(III)-salen complex gave the polymer-immobilized catalyst 122. 122 was used for the asymmetric epoxidation of unfunctionalized olens, such as that of 123 to give 124 (Scheme 32).…”
Section: Asymmetric Cyclopropanationmentioning
confidence: 99%
“…62 2.2.9 Asymmetric epoxidation. [63][64][65][66][67][68][69] Chemical modication of zinc poly(styrene-phenylvinylphosphonate)-phosphate 70 zirconium poly(styrene-isopropenylphosphonate)-phosphate, 71,72 followed by attachment of a chiral manganese(III)-salen complex gave the polymer-immobilized catalyst 122. 122 was used for the asymmetric epoxidation of unfunctionalized olens, such as that of 123 to give 124 (Scheme 32).…”
Section: Asymmetric Cyclopropanationmentioning
confidence: 99%