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- W198499234 endingPage "580" @default.
- W198499234 startingPage "534" @default.
- W198499234 abstract "Methods for desymmetrization of meso epoxides are described in this chapter. Synthetically useful, highly enantioselective catalytic methods are mainly selected and explained in detail. Asymmetric ring opening reactions of meso epoxides via S N 2 addition of azide, anilines, amines, triazole, a carboxylic acid, phenols, alcohols, water, thiols, selenols, halogens, cyanide, isocyanide, indoles, and organometallic reagents provide powerful methods for the synthesis of chiral trans -disubstituted products. Reductive ring opening of meso epoxides, rearrangement of meso epoxides under strongly basic conditions, S N 2′-type addition of organometallic reagents to allylic meso epoxides, and related desymmetrization of meso aziridines are also described. The reaction mechanism of some selected catalytic systems as well as synthetic applications are also discussed." @default.
- W198499234 created "2016-06-24" @default.
- W198499234 creator A5039224020 @default.
- W198499234 date "2012-01-01" @default.
- W198499234 modified "2023-10-09" @default.
- W198499234 title "5.22 Desymmetrization of meso Epoxide" @default.
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