A CONVENIENT SYNTHESIS OF 2-DEOXY-D-RIBOSE

DOI: 10.1246/cl.1981.1109

Source and publish data:

Chemistry Letters p. 1109 - 1110 (1981)

Update date:2022-08-03

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Authors:

Harada, Taira

Mukaiyama, Teruaki

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Article abstract of DOI:10.1246/cl.1981.1109

Successive treatment of allyltin difluoroiodide, formed in situ by the oxidative addition of stannous fluoride to allyliodide, with 1,2-O-isopropylidene-D-glyceraldehyde and phenoxyacetyl chloride results in the predominant formation of erythro homoallyle

Full text of DOI:10.1246/cl.1981.1109

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