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- W2952054559 endingPage "7826" @default.
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- W2952054559 abstract "α-Phenylsulfinyl and α-Phenylsulfonyl radicals are generated by the reactions of α-chlorosulfoxides and α-chlorosulfones with tributyltin hydride, respectively. High reaction concentration (0.2 M) is required to ensure efficient generations of these radicals. The 5-exo-type intramolecular cyclizations of these radicals are studied. The cyclization is most successful when the olefin is terminally substituted with an ester group. The sulfinyl group only induces mild diastereoselectivity on the cyclization." @default.
- W2952054559 created "2019-06-27" @default.
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- W2952054559 date "1997-06-01" @default.
- W2952054559 modified "2023-09-24" @default.
- W2952054559 title "Generation and intramolecular cyclization of α-sulfinyl and α-sulfonyl radicals" @default.
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- W2952054559 doi "https://doi.org/10.1016/s0040-4020(97)00472-9" @default.
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