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- W2034334906 endingPage "129" @default.
- W2034334906 startingPage "103" @default.
- W2034334906 abstract "The thio-Claisen rearrangement is a general and facile process that is often advantageous overthe standard Claisen rearrangement. Several asymmetric variants of the thio-Claisen rearrangement havebeen reported. The rearrangement of sulfonium salts and sulfoxides takes place even more readily. Alkenylsulfoxides and sulfilimines undergo a highly stereocontrolled cyclization to lactones and lactams,respectively, upon reaction with haloketenes; this synthetically useful process entails a [3,3]-sigmatropicrearrangement of a zwitterionic intermediate. Sulfur-containing functionalities located at the peripheryof the Claisen substrates exert a powerful influence on the outcome of the process." @default.
- W2034334906 created "2016-06-24" @default.
- W2034334906 creator A5071811984 @default.
- W2034334906 creator A5073920549 @default.
- W2034334906 creator A5077073496 @default.
- W2034334906 date "2006-01-01" @default.
- W2034334906 modified "2023-10-12" @default.
- W2034334906 title "Sulfur Participation in [3,3]-Sigmatropic Rearrangements" @default.
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