Routes to C-Glycopyranosides via Sigmatropic Rearrangements

DOI: 10.1021/jo00177a026

Source and publish data:

Journal of Organic Chemistry p. 518 - 522 (1984)

Update date:2022-08-04

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Authors:

Tulshian, Deen Bhandu

Fraser-Reid, Bert

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Article abstract of DOI:10.1021/jo00177a026

Claisen rearrangements have been applied to 1,5-anhydro-4,6-O-benzylidene-1,2-dideoxy-D-ribo-hex-1-enitol (1).The classical procedure succeeds, but the overall process is unsatisfactory because of the low conversion to the vinyl ether intermediate.Best re

Full text of DOI:10.1021/jo00177a026

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