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- W2953820503 endingPage "4105" @default.
- W2953820503 startingPage "4091" @default.
- W2953820503 abstract "Abstract An efficient one‐pot allylic alkylation of α‐enolic dithioesters (DTEs) with Morita‐Baylis‐Hillman (MBH) acetates has been devised in ethanol at room temperature. The reaction being site‐selective provided S‐allylated product exclusively with trace amount of C‐allylated one. Remarkably, some of the S‐allylated product undergoes [3,3]‐sigmatropic rearrangement to C‐allylated one under ethanol reflux. The typical feature of this protocol is the isolation of S‐allylated α‐oxoketene dithioacetals, a trisubstituted olefin, which have been further exploited toward the synthesis of thiopyrans. magnified image" @default.
- W2953820503 created "2019-07-12" @default.
- W2953820503 creator A5026814957 @default.
- W2953820503 creator A5033157405 @default.
- W2953820503 creator A5061275299 @default.
- W2953820503 creator A5077574354 @default.
- W2953820503 date "2019-07-22" @default.
- W2953820503 modified "2023-10-16" @default.
- W2953820503 title "Site‐Specific S‐Allylation of α‐Enolic Dithioesters with Morita‐Baylis‐Hillman Acetates at Room Temperature: Precursor for Thiopyrans" @default.
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