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- W4245431641 abstract "A suitable protected D-ribono-1,4-lactone derivative has been used for the straightforward chiral pool synthesis of cyclopentanoid nucleoside precursors. Thus, epoxidation followed by deoxygenation or regioselective ring opening led to nucleoside precursors modified at the positions C(4), C(4a) and C(4,4a) as well as side-chain modified derivatives. The structures of the key intermediates were determined by X-ray analyses." @default.
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- W4245431641 date "1999-08-01" @default.
- W4245431641 modified "2023-09-27" @default.
- W4245431641 title "Chiral Pool Synthesis of 4a-Substituted Carbocyclic Cyclopentanoid Nucleoside Precursors, I" @default.
- W4245431641 doi "https://doi.org/10.1515/znb-1999-0816" @default.
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