A new entry for the controlled synthesis of 2,6-dideoxy oligosaccharides

Kazunobu Toshima; Yuko Nozaki; Hatsuki Inokuchi; Masaya Nakata; Kuniaki Tatsuta; Mitsuhiro Kinoshita

doi:10.1016/0040-4039(93)85021-N

A new entry for the controlled synthesis of 2,6-dideoxy oligosaccharides

Kazunobu Toshima, Yuko Nozaki, Hatsuki Inokuchi, Masaya Nakata, Kuniaki Tatsuta, Mitsuhiro Kinoshita

Department of Applied Chemistry

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

15 Citations (Scopus)

Abstract

A novel methodology for the controlled synthesis of 2,6-dideoxy oligosaccharides by combinational use of an activated 2,6-anhydro-2-thio sugar and a deactivated 2,6-anhydro-2-sulfinyl sugar, both of which have a same leaving group at anomeric position, has been demonstrated.

Original language	English
Pages (from-to)	1611-1614
Number of pages	4
Journal	Tetrahedron Letters
Volume	34
Issue number	10
DOIs	https://doi.org/10.1016/0040-4039(93)85021-N
Publication status	Published - 1993 Mar 5

Keywords

2
6-anhydro-2-sulfinyl sugar
6-anhydro-2-thio sugar
avermectins.
glycosylation
oligosaccharide

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/0040-4039(93)85021-N

Cite this

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title = "A new entry for the controlled synthesis of 2,6-dideoxy oligosaccharides",

abstract = "A novel methodology for the controlled synthesis of 2,6-dideoxy oligosaccharides by combinational use of an activated 2,6-anhydro-2-thio sugar and a deactivated 2,6-anhydro-2-sulfinyl sugar, both of which have a same leaving group at anomeric position, has been demonstrated.",

keywords = "2, 6-anhydro-2-sulfinyl sugar, 6-anhydro-2-thio sugar, avermectins., glycosylation, oligosaccharide",

author = "Kazunobu Toshima and Yuko Nozaki and Hatsuki Inokuchi and Masaya Nakata and Kuniaki Tatsuta and Mitsuhiro Kinoshita",

year = "1993",

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doi = "10.1016/0040-4039(93)85021-N",

language = "English",

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T1 - A new entry for the controlled synthesis of 2,6-dideoxy oligosaccharides

AU - Toshima, Kazunobu

AU - Nozaki, Yuko

AU - Inokuchi, Hatsuki

AU - Nakata, Masaya

AU - Tatsuta, Kuniaki

AU - Kinoshita, Mitsuhiro

PY - 1993/3/5

Y1 - 1993/3/5

N2 - A novel methodology for the controlled synthesis of 2,6-dideoxy oligosaccharides by combinational use of an activated 2,6-anhydro-2-thio sugar and a deactivated 2,6-anhydro-2-sulfinyl sugar, both of which have a same leaving group at anomeric position, has been demonstrated.

AB - A novel methodology for the controlled synthesis of 2,6-dideoxy oligosaccharides by combinational use of an activated 2,6-anhydro-2-thio sugar and a deactivated 2,6-anhydro-2-sulfinyl sugar, both of which have a same leaving group at anomeric position, has been demonstrated.

KW - 2

KW - 6-anhydro-2-sulfinyl sugar

KW - 6-anhydro-2-thio sugar

KW - avermectins.

KW - glycosylation

KW - oligosaccharide

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U2 - 10.1016/0040-4039(93)85021-N

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AN - SCOPUS:0027458798

SN - 0040-4039

VL - 34

SP - 1611

EP - 1614

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 10

ER -

A new entry for the controlled synthesis of 2,6-dideoxy oligosaccharides

Abstract

Keywords

ASJC Scopus subject areas

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