The use of 2,6-anhydro-2-thio glycopyranosyl fluoride for a highly α-stereoselective glycosylation

Kazunobu Toshima; Satsuki Mukaiyama; Takashi Ishiyama; Kuniaki Tatsuta

doi:10.1016/S0040-4039(00)97064-3

The use of 2,6-anhydro-2-thio glycopyranosyl fluoride for a highly α-stereoselective glycosylation

Kazunobu Toshima, Satsuki Mukaiyama, Takashi Ishiyama, Kuniaki Tatsuta

Department of Applied Chemistry

Research output: Contribution to journal › Article › peer-review

19 Citations (Scopus)

Abstract

The glycosylation of 2, 6-anhydro-1-f1uoro-2-thioglycoside 1 with alcohols under various conditions proceeded smoothly at low temperature to give the corresponding α-glycosides in high yields, and the selectivity was highly independent on the conditions examined.

Original language	English
Pages (from-to)	6361-6362
Number of pages	2
Journal	Tetrahedron Letters
Volume	31
Issue number	44
DOIs	https://doi.org/10.1016/S0040-4039(00)97064-3
Publication status	Published - 1990

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)97064-3

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title = "The use of 2,6-anhydro-2-thio glycopyranosyl fluoride for a highly α-stereoselective glycosylation",

abstract = "The glycosylation of 2, 6-anhydro-1-f1uoro-2-thioglycoside 1 with alcohols under various conditions proceeded smoothly at low temperature to give the corresponding α-glycosides in high yields, and the selectivity was highly independent on the conditions examined.",

author = "Kazunobu Toshima and Satsuki Mukaiyama and Takashi Ishiyama and Kuniaki Tatsuta",

year = "1990",

doi = "10.1016/S0040-4039(00)97064-3",

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journal = "Tetrahedron Letters",

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T1 - The use of 2,6-anhydro-2-thio glycopyranosyl fluoride for a highly α-stereoselective glycosylation

AU - Toshima, Kazunobu

AU - Mukaiyama, Satsuki

AU - Ishiyama, Takashi

AU - Tatsuta, Kuniaki

PY - 1990

Y1 - 1990

N2 - The glycosylation of 2, 6-anhydro-1-f1uoro-2-thioglycoside 1 with alcohols under various conditions proceeded smoothly at low temperature to give the corresponding α-glycosides in high yields, and the selectivity was highly independent on the conditions examined.

AB - The glycosylation of 2, 6-anhydro-1-f1uoro-2-thioglycoside 1 with alcohols under various conditions proceeded smoothly at low temperature to give the corresponding α-glycosides in high yields, and the selectivity was highly independent on the conditions examined.

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U2 - 10.1016/S0040-4039(00)97064-3

DO - 10.1016/S0040-4039(00)97064-3

M3 - Article

AN - SCOPUS:0025086982

SN - 0040-4039

VL - 31

SP - 6361

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 44

ER -

The use of 2,6-anhydro-2-thio glycopyranosyl fluoride for a highly α-stereoselective glycosylation

Abstract

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