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- W2002183750 abstract "The first spirocyclic nucleoside featuring a β-hydroxyl (anti) at C5‘ has yielded to synthesis. While the OMOM functionality proved to be sensitive to the conditions necessary to incorporate heterocyclic bases, PMB protection of the carbinol was readily accommodated. The remarkably similar minimum-energy conformations of the title compounds relative to natural thymidine as deduced by Amber calculations in the gas phase are noted." @default.
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- W2002183750 date "2001-11-10" @default.
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- W2002183750 title "Spirocyclic Restriction of Nucleosides. An Analysis of Protecting Group Feasibility while Accessing Prototype <i>anti</i>-1-Oxaspiro[4.4]nonanyl Mimics" @default.
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- W2002183750 doi "https://doi.org/10.1021/ol010212g" @default.
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