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• W2790548199 abstract "The formal synthesis of lucentamycin A (1) was accomplished in 14 steps from d-serine methyl ester as a starting material. All the requisite stereogenic centers on the pyrrolidine core of 1 were controlled by SmI2-mediated cyclization. Construction of the methyl unit at the C9 position of 1 was achieved by decarbonylation of lactol 11 with stoichiometric amount of Rh(PPh3)3Cl." @default.
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• W2790548199 date "2018-04-01" @default.
• W2790548199 modified "2023-10-18" @default.
• W2790548199 title "The formal synthesis of lucentamycin A: Construction of cis -2,3-disubstituted pyrrolidine core by application of SmI 2 -DMPU system" @default.
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• W2790548199 doi "https://doi.org/10.1016/j.tetlet.2018.02.076" @default.
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