Synthesis of Isoiminosugars: Potent beta-Glucosidase Inhibitors

Lene Hyldtoft; Michael Anders Godskesen; Inge Lundt

Synthesis of Isoiminosugars: Potent beta-Glucosidase Inhibitors

Lene Hyldtoft, Michael Anders Godskesen, Inge Lundt

Research output: Chapter in Book/Report/Conference proceeding › Article in proceedings › Research

Abstract

A short synthesis of isoiminosugars have been developed. Bromolactones are diastereoselectively alkylated at C-2 followed by ring closure to the corresponding lactams. Reduction of these then gives isoiminosugars

Original language	English
Title of host publication	Abstract Book - XIXth International Carbohydrate Symposium
Place of Publication	San Diego
Publisher	International Carbohydrate Organization
Publication date	1998
Publication status	Published - 1998
Event	XIX International Carbohydrate Symposium - San Diego,CA, United States Duration: 9 Aug 1998 → 14 Aug 1998 Conference number: 19

Conference

Conference	XIX International Carbohydrate Symposium
Number	19
Country/Territory	United States
City	San Diego,CA
Period	09/08/1998 → 14/08/1998

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title = "Synthesis of Isoiminosugars: Potent beta-Glucosidase Inhibitors",

abstract = "A short synthesis of isoiminosugars have been developed. Bromolactones are diastereoselectively alkylated at C-2 followed by ring closure to the corresponding lactams. Reduction of these then gives isoiminosugars",

author = "Lene Hyldtoft and Godskesen, {Michael Anders} and Inge Lundt",

year = "1998",

language = "English",

booktitle = "Abstract Book - XIXth International Carbohydrate Symposium",

publisher = "International Carbohydrate Organization",

note = "XIX International Carbohydrate Symposium ; Conference date: 09-08-1998 Through 14-08-1998",

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T1 - Synthesis of Isoiminosugars

T2 - XIX International Carbohydrate Symposium

AU - Hyldtoft, Lene

AU - Godskesen, Michael Anders

AU - Lundt, Inge

N1 - Conference code: 19

PY - 1998

Y1 - 1998

N2 - A short synthesis of isoiminosugars have been developed. Bromolactones are diastereoselectively alkylated at C-2 followed by ring closure to the corresponding lactams. Reduction of these then gives isoiminosugars

AB - A short synthesis of isoiminosugars have been developed. Bromolactones are diastereoselectively alkylated at C-2 followed by ring closure to the corresponding lactams. Reduction of these then gives isoiminosugars

M3 - Article in proceedings

BT - Abstract Book - XIXth International Carbohydrate Symposium

PB - International Carbohydrate Organization

CY - San Diego

Y2 - 9 August 1998 through 14 August 1998

ER -