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- W2955474846 endingPage "11624" @default.
- W2955474846 startingPage "11620" @default.
- W2955474846 abstract "Abstract A 1,3‐aminothiolation was realized by reacting 2‐substituted cyclopropane 1,1‐dicarboxylates with sulfonamides and N ‐(arylthio)succinimides. Under Sn(OTf) 2 catalysis the transformation proceeded smoothly to the corresponding ring‐opened products bearing the sulfonamide in the 1‐position next to the donor and the arylthio residue in the 3‐position next to the acceptor. The procedure was extended to the corresponding selenium analogues by employing N ‐(phenylseleno)succinimides as an electrophilic selenium source." @default.
- W2955474846 created "2019-07-12" @default.
- W2955474846 creator A5079173916 @default.
- W2955474846 creator A5083595986 @default.
- W2955474846 creator A5089476171 @default.
- W2955474846 date "2019-08-07" @default.
- W2955474846 modified "2023-10-16" @default.
- W2955474846 title "Ring‐Opening 1,3‐Aminochalcogenation of Donor–Acceptor Cyclopropanes: A Three‐Component Approach" @default.
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