Synthesis of 2,6,7-trideoxy-7-C-(2,4-dichlorophenyl)-D-xylo-heptonic acid and 6-(2,4-dichlorophenyl)-D-xylo-2,3,4-tri-hydroxyhexanesulfonic acid

DOI: 10.1016/S0008-6215(00)90499-3

Source and publish data:

Carbohydrate Research p. 247 - 267 (1992)

Update date:2022-08-03

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Authors:

Kuszmann

Podanyi Podanyi

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Article abstract of DOI:10.1016/S0008-6215(00)90499-3

2,4-0-Benzylidene-L-xylose was converted via a Wittig reaction into Z-2,4-0-benzylidene-5,6-di-deoxy-6-C-(2,4-dichlorophenyl)-D-xylo-hex- 5-enitol (17), which, on hydrogenation, gave 5,6-dideoxy-6-C-(2,4-dichlorophenyl)-D-xylo-hexitol (33). tert-Butyldime

Full text of DOI:10.1016/S0008-6215(00)90499-3

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Product name:2,3,4-Tri-O-acetyl-5,6-dideoxy-6-C-(2,4-dichlorophenyl)-1-O-methanesulfonyl-D-xylo-hexitol

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