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

応用化学科

研究成果: Article › 査読

19 被引用数 (Scopus)

抄録

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.

本文言語	English
ページ（範囲）	6361-6362
ページ数	2
ジャーナル	Tetrahedron Letters
巻	31
号	44
DOI	https://doi.org/10.1016/S0040-4039(00)97064-3
出版ステータス	Published - 1990

ASJC Scopus subject areas

生化学
創薬
有機化学

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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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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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JO - Tetrahedron Letters

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

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