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Improved procedure for the room temperature asymmetric phase-transfer mediated epoxidation of α,β-unsaturated ketones

✍ Scribed by Barry Lygo; Daniel C.M To


Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
95 KB
Volume
42
Category
Article
ISSN
0040-4039

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✦ Synopsis


Studies into the factors affecting the rate of reaction in the enantioselective epoxidation of a,b-unsaturated ketones utilising Cinchona alkaloid-derived quaternary ammonium phase-transfer catalysts are reported. This has led to the identification of improved conditions for the room temperature epoxidation process, which require only 1 mol% catalyst and lead to isolation of the epoxide products in high enantiomeric excess.


📜 SIMILAR VOLUMES


Asymmetric phase-transfer mediated epoxi
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The enantioselective epoxidation of ot,~-un~turated ketones utilising Cinchona alkaloidderived quaternary ammonium phase-transfer catalysts bearing an N-anthracenylmethyl function are presented. It has been found that the O-benzyl derivatives of these catalysts in conjunction with sodium hypochlorit

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v