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- W2143663934 endingPage "542" @default.
- W2143663934 startingPage "525" @default.
- W2143663934 abstract "The diastereoselective addition of lithiated vinyl sulfoxides to enantiopure sulfinimines provides direct access to a wide assortment of allylic sulfinamides in good yields and excellent selectivities. These adducts are key precursors to differently functionalized cis- and trans-dihydropyrroles. Modulation of the protecting group on nitrogen prior to cyclization has a significant impact on the stereochemical outcome, allowing for the selective preparation of 2,5-cis- or 2,5-trans-3-sulfinyl disubstituted dihydropyrroles from a common sulfinamide intermediate. Further research on halocyclization conditions has also yielded a stereoselective synthesis of trisubstituted vinyl aziridines from these chiral sulfinamides, simply by changing the halogenating agent." @default.
- W2143663934 created "2016-06-24" @default.
- W2143663934 creator A5018742841 @default.
- W2143663934 creator A5036305825 @default.
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- W2143663934 creator A5071811984 @default.
- W2143663934 creator A5073920549 @default.
- W2143663934 creator A5090870610 @default.
- W2143663934 date "2011-12-01" @default.
- W2143663934 modified "2023-10-09" @default.
- W2143663934 title "An Approach to the Stereoselective Synthesis of Enantiopure Dihydropyrroles and Aziridines from a Common Sulfinyl-Sulfinamide Intermediate" @default.
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