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- W2369969073 abstract "A synthetic study of pactamycin is described. Enantioselective construction of the aminocyclopentitol core of pactamycin bearing five contiguous stereocenters was achieved based on an organocatalytic asymmetric aziridination of 2-cyclopentene-1-one, a regio- and diastereoselective 1,3-dipolar cycloaddition, and a rhodium-catalyzed C–H amination reaction." @default.
- W2369969073 created "2016-06-24" @default.
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- W2369969073 date "2016-05-12" @default.
- W2369969073 modified "2023-09-23" @default.
- W2369969073 title "Synthetic Study of Pactamycin: Enantioselective Construction of the Pactamycin Core with Five Contiguous Stereocenters" @default.
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- W2369969073 doi "https://doi.org/10.1021/acs.orglett.6b00761" @default.
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