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Asymmetric phase-transfer mediated epoxidation of α,β-unsaturated ketones using catalysts derived from Cinchona alkaloids

✍ Scribed by Barry Lygo; Philip G. Wainwright


Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
251 KB
Volume
39
Category
Article
ISSN
0040-4039

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✦ Synopsis


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 hypochlorite give high stereocontrol and application of this process to the enantioselective synthesis of a range of trans-~-epoxy ketones (e.e. 69-89%) is presented.


📜 SIMILAR VOLUMES


Improved procedure for the room temperat
✍ Barry Lygo; Daniel C.M To 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 95 KB

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 epo

ChemInform Abstract: Asymmetric Epoxidat
✍ S. ARAI; H. TSUGE; T. SHIOIRI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

## 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