Reaction of 2-deoxy-6-O-[2,3-dideoxy-4,6,-O-isopropylidene-2,3-(N-tosylepimino)-α -D-mannopyranosyl]-4,5-O-isopropylidene-1,3-di-N-tosylstreptamine with potassium hydrogenfluoride

DOI: 10.1016/S0008-6215(00)90582-2

Source and publish data:

Carbohydrate Research p. 363 - 368 (1992)

Update date:2022-09-26

Topics: Nucleophilic substitution Deprotection Glycosylation Reaction

Authors:

Kobayashi

Taneichi

Tsuchiya

Koga Koga

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Article abstract of DOI:10.1016/S0008-6215(00)90582-2

In a previous paper the authors reported a new method for preparation of the 2-amino-2,3-dideoxy-3-fluoro-α-D-glucopyranosyl structure by ring-opening of 2,3-dideoxy-2,3-(N-tosylepimino)-α-D-allopyranosides by potassium hydrogen fluoride (KHF₂)

Full text of DOI:10.1016/S0008-6215(00)90582-2

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Product name:2-Deoxy-6-O-(2,3-dideoxy-3-fluoro-4,6-O-isopropylidene-2-tosylamido-α-D-altropyranosyl)-4,5-O-isopropylidene-1,3-di-N-tosylstreptamine

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