SYNTHESIS OF METHYL 2-ACETAMIDO-2,3,6-TRIDEOXY-β-L-lyxo-HEXOPYRANOSIDE

DOI: 10.1016/0008-6215(83)88112-9

Source and publish data:

Carbohydrate Research p. 227 - 238 (1983)

Update date:2022-08-05

Topics: Synthesis Column chromatography NMR spectroscopy Reactions Triflation Decomposition Isolation Precipitate Thin-layer chromatography (TLC) Spectrophotometer Mass spectrometry Microanalysis

Authors:

Gallagher, Timothy F.

Horton, Derek

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Article abstract of DOI:10.1016/0008-6215(83)88112-9

The title glycoside, having the daunosamine structure but with amination at C-2 instead of C-3, was synthesized in nine steps from 2-acetamido-2-deoxy-D-glucose.The sequence also provided preparative access to methyl 2-acetamido-2,3-dideoxy-α-D-ribo-hexop

Full text of DOI:10.1016/0008-6215(83)88112-9

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Product name:methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-trifluoromethylsulfonyl-α,β-D-glucopyranoside

Cas No:86988-15-0

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