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C2‑Symmetric Cyclic Selenium-Catalyzed Enantioselective Bromoaminocyclization

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Figshare2016-02-20 更新2026-04-29 收录
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https://figshare.com/articles/dataset/_i_C_i_sub_2_sub_Symmetric_Cyclic_Selenium_Catalyzed_Enantioselective_Bromoaminocyclization/2448820
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A catalytic asymmetric bromocyclization of trisubstituted olefinic amides that uses a C2-symmetric mannitol-derived cyclic selenium catalyst and a stoichiometric amount of N-bromophthalimide is reported. The resulting enantioenriched pyrrolidine products, which contain two stereogenic centers, can undergo rearrangement to yield 2,3-disubstituted piperidines with excellent diastereoselectivity and enantiospecificity.
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2016-02-20
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